Trigeminal neuralgia - Connective tissue disease Factor. Last reviewed for CCPS 10 March 1995.. Preliminary questions [8154]. 8603 [1] there is some evidence that a connective tissue disease may be a factor in the development of the condition under consideration.. 8184 - the veteran has suffered from a connective tissue disease at some time.. 6563 [2] the veteran has had scleroderma at some time.. or. 8615 [3] the veteran has had Sjogrens syndrome at some time.. or. 2576 [4] the veteran has had systemic lupus erythematosus at some time.. or. [5]8616. the veteran has had dermatomyositis at some time.. or. 8617 [6] the veteran has had mixed connective tissue disease at some time.. 8186 [7] the veteran suffered from the identified illness or injury, a connective tissue disease, prior to the clinical onset of trigeminal neuralgia. [8]. 8187 - the veteran has established the causal connection between the identified illness or injury, a connective tissue disease, and operational service for the ...
Undifferentiated connective tissue diseases (UCTDs) are clinical entities characterised by signs and symptoms suggestive of a systemic autoimmune disease, which do not fulfil the diagnostic criteria for a defined connective tissue disease. Lung involvement can complicate the course and management of the disease, often determining a worse outcome. Respiratory dysfunction as the first clinical manifestation has seldom been reported. We describe a case of a female patient who developed significant respiratory dysfunction as the principal clinical sign. Video-assisted thoracoscopy was performed and a histological pattern of nonspecific interstitial pneumonia (NSIP) was found. A pathological diagnosis suggested careful follow-up with extensive immunological screening which then detected Raynauds phenomenon and positivity of antinuclear antibodies. After a multidisciplinary discussion (pneumologist, radiologist, pathologist and rheumatologist) a final diagnosis of NSIP associated with UCTD was made. The
How undifferentiated connective tissue disease (UCTD) is diagnosed through its symptoms, family history, physical examination, x-rays, and CT scans.
(Update) Donna C: Undifferentiated Connective Tissue Disease (UCTD) For the most part I have still been doing very good. Some little setbacks here and there...
Objective. To review the diagnoses after 5 years in patients who were identified within 12 months of the onset of well established and undifferentiated connective tissue diseases CTD ; to examine death rates and disease remissions in these patients. Methods. This inception cohort of 410 patients was identified in 10 academic rheumatology...
Undifferentiated Connective Tissue Disease stories from our community of patients. Read how these patients from all walks of life got back into their game of life.
A rheumatology biorepository will be created to permit comparative analyses between the rheumatic diseases in order to increase the understanding of disease pathogenesis. Patients diagnosed with rheumatic diseases are invited to participate in this study. These rheumatic diseases include, but are not limited to: adult onset Stills disease, ankylosing spondylitis, psoriatic arthritis, reactive arthritis, antiphospholipid syndrome, systemic lupus erythematosus, Behcets disease, dermatomyositis, polymyositis, giant cell arteritis and other vasculitides, Lymes disease, mixed connective tissue disease, polymyalgia rheumatica, rheumatoid arthritis, sarcoidosis, systemic sclerosis (scleroderma), Sjogrens syndrome, and undifferentiated connective tissue disease. Healthy volunteers are also invited to participate in this study ...
Scleroderma (especially CREST syndrome). Mixed connective tissue disease Systemic lupus erythematosus Rheumatoid arthritis Dermatomyositis. Which occurs more frequently, primary or secondary pulmonary hypertension?. Primary (unexplained) pulmonary hypertension is a rare disorder. Secondary pulmonary hypertension is seen considerably more often in practice.. What population group is most frequently affected by primary pulmonary hypertension?. Although primary pulmonary hypertension occurs in both sexes and virtually all age groups, it has a tendency to affect young females. The female-to-male predominance is 1.7:1, and the mean age is 36 years.. Is surgical therapy now an option for patients with pulmonary hypertension secondary to chronic recurrent thromboembolism?. Appropriate prevention of recurrent thromboembolism continues to be extremely important. In addition to this prevention, it is now possible to remove organized thrombus surgically from the proximal pulmonary arteries of patients with ...
This week, I was called to evaluate a young man with several aneurysms (ballooning of his blood vessels) and a dilated (widened) aorta. The medical team thought he had a connective tissue disease because a family member also had a connective tissue disease-she had lupus. Unfortunately, doctors can mean very different things when they talk about a connective tissue disease; this is a common source of confusion for doctors and patients alike. After reading this post, I hope youll be able understand the difference.. Connective tissue is the stuff that holds your body together. That is, the bones, ligaments, tendons, cartilage, fat, and glue that keeps all your organs in place. Two very different types of diseases can affect these tissues-you can have problems in MAKING the connective tissues, or these tissues can be ATTACKED by the bodys own immune system.. In the first type of connective tissue disease, the body is unable to produce strong connective tissues. Its like trying to build ...
The conceptual study of connective tissue diseases as one of causative factors in Interstitial lung diseases (ILDs) : both modern and ayurveda perspective ;patients with ILDs come with the onset of progressive exertional dyspnea or a persistent nonproductive cough. Hemoptysis , wheezing and chest pain may be present. Often , the identification of interstitial opacities on chest X-ray focuses the diagnostic approach on one of the ILDs. Rheumatoid arthritis is one of connective and autoimmune diseases which cause ILDs.. inflammation in the air space and alveolar walls and interstitial fibrosis are present due to autoimmunity.. the presence of jts pain , stiffness and deformity like swan neck etc with +ve antinuclear antibodies and anti- immunoglobulin antibodies ( RA factors ) confirm the diagnosis , however these tests are +ve even in absence of defined connective tissue diseases. ILDs are characterized as a significant part of a multiorgan process , as may occur in the connective tissue diseases ...
RP is an exaggerated vascular response to cold temperature or emotional stress, primarily seen in young women. It is classified into primary or idiopathic without underlying disease and secondary when it is related to various medical problems.1,2 Clinical criteria are used to distinguish between patients with uncomplicated or primary RP, and those with secondary RP. The suggested criteria for primary RP are symmetric attacks; the absence of tissue necrosis, ulceration or gangrene; the absence of a secondary cause on the basis of a patients history and general physical examination; normal nailfold capillaries; a negative test for antinuclear antibody; and a normal erythrocyte sedimentation rate.2,3 The most common diseases associated with secondary RP are scleroderma, mixed connective tissue disease, systemic lupus erythematosus, occlusive vascular disease, drug effects, haematological abnormalities, and use of vibrating tools.1,3 Primary RP occasionally evolves into a connective tissue disease, ...
LeRoy, EC, Black, C, Fleischmajer. Scleroderma (Systemic Sclerosis): classification, subsets, and pathogenesis. J Rheumatology. vol. 15. 1988. pp. 202-5. (This article lays the foundation for how most people classify and characterize scleroderma.) Steen, VD. Pregnancy in Scleroderma. Rheum Dis Clin N Am. vol. 33. 2007. pp. 345-58. (Dr. Steen is a leading expert in the area of systemic sclerosis.) Steen, VD. Pregnancy in women with systemic sclerosis. Obstet Gynecol. vol. 94. 1999. pp. 15-20. Miniati, I, Guiducci, S, Mecacci, F. Pregnancy in systemic sclerosis. Rheumatology. vol. 47. 2008. pp. iii16-iii18. Chung, L, Flyckt, RLR, Colón, I. Outcomes of pregnancies complicated by systemic sclerosis and mixed connective tissue disease. Lupus. vol. 15. 2006. pp. 595-9. Subcommittee for scleroderma criteria of the American Rheumatism Association Diagnostic and Therapeutic Criteria Committee: Preliminary criteria for the classification of systemic sclerosis (scleroderma). Arthritis Rheum. ...
Purple and Blue Awareness Ribbon Causes & Meanings What causes are associated with the purple and blue awareness pin? * Adult-Onset Stills Disease * Alternating Hemiplegia * Childhood Stroke * Cult Awareness * Mixed Connective Tissue Disease (MCTD) * Pediatric Rheumatic Diseases * Pediatric Stroke * Preeclampsia * Rheumatoid Arthritis * Rheumatoid Disease
Results A total of 221 NPC, corresponding to 197 patients, 167 females (84.8%) and 30 males (15.2%) aged from 9 to 90 years were reviewed. One hundred and thirty eight (62.4%) patients had no definitive diagnosis, 53 patients (24%) had SSc, 7 (3.2%) had mixed connective tissue disease, 3 (1.4%) had dermatomyositis/polymyositis (DM/PM), and 3 (1.4%) antiphospholipid syndrome (APS).. Raynauds phenomenon (RP) alone was the most frequent reason for requesting NCP (33% of the cases), and combined with ANA positivity accounted for another 30.8% of the requests. RP was present in 73.3% of the patients, acrocyanosis in 16.3%, livedo reticularis and puffy hands accounted for 8.6% each one. Anti-nuclear antibodies (ANA) were positive in 59.7%, anti-centromere antibodies were present in 21.3%, anti-topoisomerase I and SSA/SSB in 5.1% of the cases.. One hundred and fifty nine (71.9%) NCP were considered abnormal. The most frequent specific disease pattern was the early one (Cuttolo) in 15%. The most ...
Rheumatoid arthritis, Bechterews disease, arthritis, mixed connective tissue disease with articular manifestations (scleroderma, systemic lupus erythematosus, etc.), articular diseases associated with endocrine disorders, neurological diseases and blood disorders, pain resulting from osteoporosis, tendons, ligaments and muscles pain, hip arthritis, knee joint inflammation, other forms of joints inflammation, post-injury cases, rehabilitation after musculoskeletal surgery, especially spine and joints surgery (joint replacement), joint replacement pre-operation, scoliosis, spinal pain, and joint injury due to metabolic exchange disorders.. ...
In the United States, more than 50 million adults and 300,000 children live with arthritis. Costing the U.S. economy $156 billion dollars a year, arthritis affects one in five Americans and causes more activity limitation than heart disease, cancer or diabetes. The Chicago Walk to Cure Arthritis will help those living with arthritis by supporting programs, research and advocacy initiatives as well as fund crucial research aimed at finding a cure for the disease.. At the walk, local honorees Amanda Barnes and Krista Bauman will share their inspiring stories about living with arthritis. Amanda, diagnosed at only five years old, was diagnosed with polyarticular juvenile idiopathic arthritis. Krista was diagnosed with mixed connective tissue disease in 2011 and has a combination of rheumatoid arthritis, lupus and scleroderma. I want to follow my dreams and find a cure for arthritis. I want to help other kids going through the same thing as me, says youth honoree Amanda Barnes. My hopes for the ...
TY - JOUR. T1 - T cell immunity in connective tissue disease patients targets the RNA binding domain of the U1-70kDa small nuclear ribonucleoprotein. AU - Greidinger, Eric L.. AU - Foecking, Mark F.. AU - Schäfermeyer, Kim R.. AU - Bailey, Craig W.. AU - Primm, Shannon L.. AU - Lee, David R.. AU - Hoffman, Robert W.. PY - 2002/9/15. Y1 - 2002/9/15. N2 - Although the T cell dependence of autoimmune responses in connective tissue diseases has been well established, limited information exists regarding the T cell targeting of self Ags in humans. To characterize the T cell response to a connective tissue disease-associated autoantigen, this study generated T cell clones from patients using a set of peptides encompassing the entire linear sequence of the 70-kDa subunit of U1 snRNP (U1-70kDa) small nuclear ribonucleoprotein. Despite the ability of U1-70kDa to undergo multiple forms of Ag modification that have been correlated with distinct clinical disease phenotypes, a remarkably limited and ...
TY - JOUR. T1 - The short-term role of corticosteroid therapy for pulmonary arterial hypertension associated with connective tissue diseases. T2 - Report of five cases and a literature review. AU - Kato, M.. AU - Kataoka, H.. AU - Odani, T.. AU - Fujieda, Y.. AU - Otomo, Kotaro. AU - Oku, K.. AU - Horita, T.. AU - Yasuda, S.. AU - Atsumi, T.. AU - Ohira, H.. AU - Tsujino, I.. AU - Nishimura, M.. AU - Koike, T.. PY - 2011/10/1. Y1 - 2011/10/1. N2 - Pulmonary arterial hypertension (PAH) is a life-threatening complication in connective tissue diseases (CTD). It remains controversial whether immunosuppressive therapy is useful for PAH associated with CTD (PAH-CTD). The Dana Point algorithm does not refer such treatments in patients with PAH-CTD due to the lack of evidence. However, some case reports have shown the potential efficacy of immunosuppression for PAH-CTD. Here we report five cases of PAH-CTD treated with corticosteroids and discuss the current management of PAH-CTD with immunosuppressive ...
ILD is most commonly found in systemic sclerosis at a prevalence rate of 25% to 90%, Dr. Fischer said. It is also found less frequently in polymyositis and dermatomyositis, RA, Sjögrens syndrome, and systemic lupus erythematosus. If rheumatologists are treating patients with known connective tissue disease, they should take steps to determine if possible ILD is connective tissue disease¬ associated, Dr. Fischer said. Recognition of the exact disease would affect treatment decisions and the prognosis for these patients. Its important for the patients outcome to see where they fit, he said.. ...
Study shows HHV-6 reactivation is disproportionately elevated among patients with autoimmune connective tissue disease. A new study from Italy indicates that HHV-6 reactivation is selectively increased among patients suffering from autoimmune connective tissue diseases (ACTD). Low levels of HHV-6 DNA were detected in the serum of 26% of ACTD patients, which was significantly greater than that observed amongst controls (P , 0.0002). The authors used a highly sensitive assay and the median viral load for these patients was under 100 copies/ml, which would fall below the current level of detection at most clinical laboratories. The group also found a significant association between HHV-6 reactivation and the active disease state for lupus erythematosus (P = 0.021). By contrast, the rate of EBV viremia was similar in patients and controls groups, while CMV, HHV-8, and parvovirus B19 viremia was not detected in any subject.. In the paper, published in the Journal of Medical Virology this month, the ...
Complex Treatment of Children Affected by Undifferentiated Connective Tissue Dysplasia Combined with Bone Mineral Density Reduction
Complex Treatment of Children Affected by Undifferentiated Connective Tissue Dysplasia Combined with Bone Mineral Density Reduction
Culture anything you already know and any risks taken by means of self-medicating distressing positive and reasonably well localized in the following formula: Mmol number of patterns usually present, the only interventions dysfunction erectile multiple sclerosis viagra necessary in some countriessimilar effectiveness. This now also available these do not speak english. Fig. Comput biol med ; :. Montori vm, devereaux pj, adhikari nk, burns ke, eggert ch, briel m et al. Cuboidal epithelium with eosinophilic cytoplasm; a peritubular hyaline rim of connective tissue disease jia mixed connective tissue. Samaritans. Craniopharyngioma patients have end-stage renal disease. Ocd reported to slow radiographic progression of diabetic foot this is the anti-arrhythmic of choice is based on history, electrocardiograph ecg changes, headache, fatigue, sleep disturbance, reduced libido, muscle strength, and form supplied. Mda-mb- skin cancer also showed that by the active phase or by catheterization to exclude ...
Background Pulmonary hypertension (PH) can develop in connective tissue disease associated interstitial lung disease (CTD-ILD), and contributes to increased morbidity and mortality. However, except...
Background: Connective tissue disease (CTD) is a group of inflammatory disorders of unknown aetiology. Patients with CID often report hypersensitivity to nickel. We examined the frequency of delayed type hypersensitivity (DTH) (Type IV allergy) to metals in patients with CTD. Methods: Thirty-eight patients; 9 with systemic lupus erythematosus (SLE), 16 with rheumatoid arthritis (RA), and 13 with Sjogrens syndrome (SS) and a control group of 43 healthy age- and sex-matched subjects were included in the study. A detailed metal exposure history was collected by questionnaire. Metal hypersensitivity was evaluated using the optimised lymphocyte transformation test LTT-MELISA (R) (Memory Lymphocyte Immuno Stimulation Assay). Results: In all subjects, the main source of metal exposure was dental metal restorations. The majority of patients (87%) had a positive lymphocyte reaction to at least one metal and 63% reacted to two or more metals tested. Within the control group, 43% of healthy subjects ...
WHO Group 1 PH (PAH, pulmonary arterial hypertension) is a progressive and chronic disease. There currently is no cure. In PAH, the arteries in the lungs become narrow, thickened or stiff, which causes high blood pressure in the lungs. The disease can present in several forms, one of which is PAH associated with connective tissue disease (CTD-PAH), such as scleroderma, CREST syndrome and lupus. Research has found that this particular form of PAH is difficult to treat and patients have worse outcomes compared to people with other types of PAH. Two groups of researchers looked at different approaches to treating CTD-PAH using PH-targeted medications.. Selexipag therapy. The European Respiratory Journal published the findings of one study on the use of selexipag (Uptravi®) in patients with CTD-PAH. (https://www.ncbi.nlm.nih.gov/pubmed/28818881) Sean Gaine, M.D. - National Pulmonary Hypertension Unit, Mater Misericordiae University Hospital in Dublin - led an international team of researchers to ...
This multicenter study will attempt to determine the epidemiologic, clinical, serologic and immunogenetic factors associated with patients who develop scleroderma/systemic sclerosis after silicone prosthesis implantation or silicone injection. This will be accomplished by comparing these patients to groups of appropriately matched patients with idiopathic scleroderma/systemic sclerosis without silicone exposure, and appropriately matched volunteers who have received similar silicone implants or injections and have not developed symptoms, physical examination findings, or laboratory abnormalities associated with autoimmune/connective tissue diseases. Patient and physician questionnaires will be self-administered, and will collect data regarding: the number and types of implanted silicone devices or injections; the indications for and nature of the surgical procedures; peri- and post-operative complications; initial and subsequent clinical presentations; and therapy and clinical course of the ...
This ACD course teaches, from a dermatological perspective, about the most commonly encountered Connective Tissue Disease including autoimmune disorders such as Lupus, Dermatomyositis and Scleroderma.
This article reviews the associations of occupational and environmental exposures relevant to connective tissue diseases, and in particular systemic sclerosis.
To determine the clinical significance of anticentromere (ACA) and anti Scl-70 antibodies in an English population with connective tissue diseases, we examined the sera of 150 patients, including 40...
This article will inform you about lupus and connective tissue disease as well as other similar disorders that are interconnected with the disease.
Connective tissue diseases are generally rare with varying prevalence. Accurate diagnosis and specialist care are key to proper management.
Background Interstitial pneumonia in connective tissue diseases (CTD-IP) featuring inflammation and fibrosis is usually a leading cause of death in CTD-IP individuals. by histology, circulation cytometry and molecular biology. Capital t cell subsets included in the procedure of CTD-IP had been described, while the regulatory features of MSCs separated from the bone tissue marrow of regular people (HBMSCs) on cytotoxic Capital t cells and CTD-UIP HLFs had been looked into in vitro. Outcomes Higher frequencies of cytotoxic Capital t cells had been noticed in the lung and peripheral bloodstream of CTD-IP individuals, followed with a decreased regulatory Capital t cell (Treg) level. CTD-UIP HLFs secreted proinflammatory cytokines in mixture with upregulation of -clean muscle mass actin (-SMA). The addition of HBMSCs in vitro improved Tregs SC-514 concomitant with decreased cytotoxic Capital t cells in an fresh cell model with prominent cytotoxic Capital t cells, and advertised Tregs growth in ...
Uveitis Caused by Connective Tissue Disease - Etiology, pathophysiology, symptoms, signs, diagnosis & prognosis from the MSD Manuals - Medical Professional Version.
Study Connective Tissue Disease flashcards from Rebecca Thomas's class online, or in Brainscape's iPhone or Android app. ✓ Learn faster with spaced repetition.
University of Minnesota Health physicians are available to help you with some of the most advanced treatments to relieve pain from connective tissue disease and improve your quality of life.
A Herculean process really and you need to be applauded for locating something that mixes the three issues together in one go. Every cell in the body needs iodine. Unlike hierarchical data structure that require specific entrance points to find records in a hierarchy, network data structures can by entered and traversed more flexibly. I like to recommend counting calories and holding a diet journal at the least as soon as in your life for a minimum of 4-12 consecutive weeks or till you obtain unconscious competence. This way you will be able to determine what you are giving your pet. Foodstuffs that are rich in soluble fibres embrace seasonal fruits, beans, lentils, oat bran, dried peas, leafy greens connective tissue disease and nutrition barley. What should you eat and drink to produce enough milk and to get enough nutrients for your baby and yourself. We love using spinach as a base for a salad, and youll reap the greatest dietary advantages when its raw. By comparing the prices you could ...
Background/Purpose: Patients with Systemic Autoimmune Rheumatic Disease (SARD) often have a prolonged pre-clinical phase during which they are anti-nuclear antibody (ANA) positive but lack clinical symptoms. It has been proposed that progression from asymptomatic autoimmunity to clinical disease is accompanied by immunologic changes that could be used as predictors of disease development. Our objective was to identify cyto/chemokine abnormalities in ANA+individuals who lack sufficient criteria for a diagnosis of SARD. Methods: ANA+ individuals who: 1) lacked clinical symptoms of SARD (ANA No Symptoms, ANS); 2) had a least one clinical symptom of SARD (Undifferentiated Connective Tissue Disease, UCTD); or 3) had a recently diagnosed steroid and immunosuppressive naïve SARD were recruited, and compared with ANA- healthy controls (HC). The levels of 30 cyto/chemokines were measured, 29 by Luminex and one (BAFF) by ELISA. Peripheral blood interferon (IFN)-induced and BAFF gene expression was ...
I lost my Mariel to Interstitial Lung Disease caused by Undifferentiated Connective Tissue Disease. Barely six weeks after we checked with a dermatologist to complain about some ordinary rashes and fever. ( We were even discharged earlier at another hospital for what they thought was merely a viral infection, after ruling out Dengue ). C3…
Non-specific interstitial PNA (NSIP) - basilar-predominant process, ground glass opacities and reticular pattern on imaging, 80% of patients will have fibrotic pattern as well, seen in patients with undifferentiated connective tissue disease, SLE, Sjogrens, Systemic sclerosis, and ...
Hello, I havent posted in a long time - my official diagnosis is undifferentiated connective tissue disease with signed of lupus and Sjögrens syndrome. My last rheumatology check up was almost a...
She has masters degrees in applied, clinical early signs of pregnancy in my dog community ssigns. i want to bookmark everything you ever write. Be sure your schedule is coordinated with other teachers in the school. But the real trouble do a force much larger than they are-one which they cant even pinpoint, and so have little chance to fight. Your babys size may make you feel uncomfortable. Then they were born and their parents wouldnt let you. Plan for some decompression time between conferences. A doctor can sgns you from this requirement. One question that single parents often have is how to make quality time for their children, despite their exhaustion. O quality of education. A recent Consumers Research magazine report on the risk to health from some fluorescent lamps suggested new probes by industry and the government. Your tips are super helpful, thank you. In case undifferentiated connective tissue disease and pregnancy are on the look-out for schools in Punjabi Bagh from the best ...
The INNO-LIAr ANA Update is a qualitative test detecting antibodies to several different antigens, most of which are recombinantly made, with the exception of SSA/Ro60 and histones (natural), and SmD and ribosomal P (synthetic). The LIA-SCAN ANA provides a quantitative read-out of the INNO-LIAr ANA Update results. The cut-off value of the different antigen lines was optimized using an in-house set of 955 samples. The assay specificity was validated at multiple sites using a different set of 330 samples obtained from 158 apparently healthy blood donors, 100 patients with a variety of infections, 20 with Wegeners granulomatosis, 20 with inflammatory bowel disease, 20 with primary antiphospholipid syndrome, and 12 with psoriatic arthritis. The INNO-LIAr ANA Update reactivity using the optimized cut-off was tested in 147 patients with scleroderma, 93 with Sjögrens disease, 40 patients with systemic lupus erythematosus (SLE), 40 with rheumatoid arthritis (RA), 39 with mixed connective tissue ...
This sounds as if you were born with an auto-immune (self attacking self) connective tissue disease. Connective tissue is what holds your cells together, and there are a few connective tissue diseases. In my family, we get red, inflammed connective tissue and like you, it hurts to lay or sit or get touched or anything. I was born with it, it is genetic. I would suggest that you research connective tissue diseases or find a specialist and a good teaching hospital (like a university medical center) that would be willing to do the work and tests for you. Bless you, what a life that is. ...
CollagenThe most important nutrient for stronger connective tissue is Collagen. … The optimal way to get the right amount of collagen is through your diet. … Another vital nutrient that helps to support healthy connective tissue is glucosamine. … One of the most vital components of cartilage is chondroitin.More items ...
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A heterogeneous group of disorders, some hereditary, others acquired, characterized by abnormal structure or function of one or more of the elements of connective tissue, i.e., collagen, elastin, or the mucopolysaccharides ...
TY - JOUR. T1 - Severe rhizomelic chondrodysplasia punctata in a fetus due to maternal mixed connective tissue disorder. AU - Nayak, S. S.. AU - Adiga, P. K.. AU - Rai, L.. AU - Girisha, K. M.. PY - 2012. Y1 - 2012. N2 - Maternal systemic lupus erythematosus and autoimmune diseases have been extremely rarely reported to cause rhizomelic chondrodysplasia punctata. We report on a fetus aborted spontaneously at 21 weeks of gestation due to complications of maternal mixed connective tissue disorder. The fetus had micrognathia, a depressed nasal bridge, flat nose, long philtrum, short columella and rhizomelia. Radiographic study showed stippling of carpal and tarsal bones, short humeri and coronal clefts in the vertebrae. Ossification centers were present at the lower end of the femora and upper end of the tibiae.. AB - Maternal systemic lupus erythematosus and autoimmune diseases have been extremely rarely reported to cause rhizomelic chondrodysplasia punctata. We report on a fetus aborted ...
undifferentiated connective tissue disease answers are found in the Tabers Medical Dictionary powered by Unbound Medicine. Available for iPhone, iPad, Android, and Web.
TY - JOUR. T1 - A 61-year-old woman with osteomalacia and a thoracic spine lesion. AU - Marshall, Ann E.. AU - Martin, Sarah E.. AU - Agaram, Narasimhan P.. AU - Chen, Jey Hsin. AU - Horn, Eric. AU - Douglas-Akinwande, Annette C.. AU - Hattab, Eyas M.. PY - 2010/3. Y1 - 2010/3. N2 - Phosphaturic mesenchymal tumor, mixed connective tissue variant (PMT-MCT) is a rare, largely benign, mesenchymal neoplasm almost invariably associated with oncogenic osteomalacia. It is generally found in the soft tissue and bone of the extremities. We report a case of a 61-year-old female with long-standing osteomalacia who was found to have PMT-MCT of the thoracic spine. There have been very few previously reported cases of PMT involving the spinal vertebrae and neuropathologists should be aware of this lesion. Recognition of PMT-MCT is critical for optimal patient care since complete surgical resection without additional therapy is curative.. AB - Phosphaturic mesenchymal tumor, mixed connective tissue variant ...
Connective tissue diseases by Graham R. V. Hughes; 4 editions; First published in 1977; Subjects: Collagen diseases, Connective Tissue Diseases, Connective Tissue, Diseases, Connective tissues, Internet Archive Wishlist
What is CTD-ILD? Connective tissue disease-associated interstitial lung disease (CTD-ILD) is a lung disease that may happen to some people with a connective tissue disease.
A total of 187 specimens from 142 subjects with rheumatoid arthritis, systemic lupus erythematosus, other connective tissue diseases, and controls were placed in cell culture. Specimens from 119 of the subjects grew, lasting over 2 yr in several instances. No evidence of virus infection has been found by a variety of sensitive methods, including cell fusion. Other approaches have likewise failed thus far to implicate any virus in the pathogenesis of rheumatoid arthritis.. ...
Background and objectives: The overlap between antineutrophil cytoplasmic antibody (ANCA) associated glomerulonephritis (ANCA-GN) and connective tissue diseases (CTD) has been reported mainly as case series in the literature. Frequency of this association, as well as presentation and outcomes are unknown. Materials and Methods: Patients from the Maine-Anjou ANCA-associated vasculitides (AAV) registry with ANCA-GN diagnosed between 01/01/2000 and 01/01/2018, ANCA positivity, and at least six months of follow-up, were included. Results: 106 out of 142 patients fulfilled the inclusion criteria and were analyzed. CTD was present at ANCA-GN diagnosis in 16 (15.1%) patients. The most common CTD were rheumatoid arthritis, Sjogren syndrome and systemic sclerosis. Compared to the control group, females were more represented in the CTD group (75%, p = 0.001). Renal presentation was comparable between groups, including the pathological analysis of renal biopsies. Patients of CTD group presented a higher rate of
Breast implants and connective tissue diseases answers are found in the Evidence-Based Medicine Guidelines powered by Unbound Medicine. Available for iPhone, iPad, Android, and Web.
TY - JOUR. T1 - Peripheral sensorimotor and autonomic neuropathy associated with systemic lupus erythematosus. T2 - Clinical, pathological and immunological features. AU - Mccombe, P. A.. AU - Mcleod, J. G.. AU - Pollard, J. D.. AU - Guo, Y. P.. AU - Ingall, T. J.. PY - 1987/4. Y1 - 1987/4. N2 - The clinical features and pathological findings in the sural nerves are described of 7 patients with peripheral neuropathy; in 4 cases the criteria for diagnosis of systemic lupus erythematosus (SLE) were satisfied and in 3 other cases there was serological evidence of an undifferentiated connective tissue disease, most probably SLE. The peripheral neuropathy was of a chronic sensorimotor type with predominantly sensory features and gradual onset. In 2 cases the presentation was asymmetric. One patient had autonomic dysfunction. The pathological findings in the biopsied sural nerves were those of axonal degeneration and vasculitis. In 6 nerves there was increased expression of Class II (Ia) antigen ...
Ceftriaxone therapy of chronic inflammatory arthritis. A double-blind placebo controlled trial. Arch Intern Med. 1990 Aug;150(8):1677-82.. In a placebo-controlled, double-blind study of 60 patients with inflammatory arthritis - rheumatoid arthritis (RA), psoriatic arthritis (PsA), vasculitis, and undifferentiated connective tissue disease (UCTD) - who were positive for Lyme disease (borrelia burgdorferi), patients were randomized to be in one of two study arms to either receive an inactive placebo or the antibiotic, ceftriaxone, 2 grams/day, intravenously for 2 weeks. Nearly half of the antibiotic group (19/40 patients) experienced improvement as compared with the placebo group (2/20 patients), who were later able to elect to receive ceftriaxone therapy. Of 58 patients who were treated with IV ceftriaxone, 27 were notably improved at follow-up, 13-24 months later, and responses were seen in all forms of arthritis (RA 5/12, PsA 5/8, vasculitis 3/5, and UCTD 14/33). Of these 27 patients, 16 ...
This week, I was called to evaluate a young man with several aneurysms (ballooning of his blood vessels) and a dilated (widened) aorta. The medical team thought he had a connective tissue disease because a family member also had a connective tissue disease-she had lupus. Unfortunately, doctors can mean very different things when they talk about a connective tissue disease; this is a common source of confusion for doctors and patients alike. After reading this post, I hope youll be able understand the difference.. Connective tissue is the stuff that holds your body together. That is, the bones, ligaments, tendons, cartilage, fat, and glue that keeps all your organs in place. Two very different types of diseases can affect these tissues-you can have problems in MAKING the connective tissues, or these tissues can be ATTACKED by the bodys own immune system.. In the first type of connective tissue disease, the body is unable to produce strong connective tissues. Its like trying to build ...
Patients with uncharacteristic inflammatory symptoms such as long-standing fatigue or pain, or a prolonged fever, constitute a diagnostic and therapeutic challenge. The aim of the present study was to determine if an extended immunophenotyping of lymphocytes and monocytes including activation markers can define disease-specific patterns, and thus provide valuable diagnostic information for these patients. Whole blood from patients with gram-negative bacteraemia, neuroborreliosis, tuberculosis, acute mononucleosis, influenza or a mixed connective tissue disorders, as diagnosed by routine culture and serology techniques was analysed for lymphocyte and monocyte cell surface markers using a no-wash, no-lyse protocol for multi-colour flow cytometry method. The immunophenotyping included the activation markers HLA-DR and CD40. Plasma levels of soluble TNF alpha receptors were analysed by ELISA. An informative pattern was obtained by combining two of the analysed parameters: (i), the fractions of HLA-DR
Reversible vasospasm of the extremities occurs as an isolated symptom in the absence of underlying disease (primary Raynaud phenomenon) or in association with other disorders (secondary Raynaud phenomenon). It has been reported that Raynaud phenomenon is associated with connective tissue diseases, but the frequency and types of diseases that eventually develop are not well established. Spencer-Green conducted a systematic literature search to assess the rates and predictors of transition to secondary disease after a primary diagnosis of Raynaud phenomenon.. A total of 639 patients with primary Raynaud phenomenon were identified from 10 studies. The average length of study follow-up was four years. The average duration of Raynaud phenomenon in the study subjects was 12.3 years. During follow-up, 12.6 percent (81 patients) developed a secondary disorder. Eighty of these cases were connective tissue diseases. Two thirds of the cases of connective tissue disease were attributed to systemic ...
Since immune responses play a major role in the development of connective tissue diseases, it is not surprising that a number of laboratory studies reflect these responses. Prior to the 1940s when rheumatoid and LE factors became widely known, one relied mainly on erythrocyte sedimentation rate and serum electrophoresis to identify protein abnormality. Elevated sedimentation rate depends on rouleaux formation, and rouleaux formation is dependent upon large asymmetric molecules of fibrinogen and gamma globulin in plasma. The demonstration of gamma globulin has become the cornerstone of the immunologists edifice. It is amazing to see how the subspecialty of immunology has mushroomed to involve the many facets of disease processes such as connective tissue diseases, skin diseases, gastrointestinal diseases, renal diseases, and cancer. More recently, immune deficiency diseases have included the pediatrician in the ever-enlarging field of immunology as has the modern-day discovery of human leukocyte antigen
Scope. This guideline describes appropriate use of antinuclear antibody (ANA) testing in the diagnosis of connective tissue disease (CTD), also referred to as systemic rheumatic disease. It applies only to individuals 17 years of age and over. The guideline does not address ANA testing in the investigation of unexplained infertility, adverse pregnancy outcomes, liver disease or thrombotic disorders.. RECOMMENDATION 1: ANA testing not indicated. ANA testing should not be ordered unless a connective tissue disease is a significant clinical possibility.. ANA testing is not helpful in confirming a diagnosis of rheumatoid arthritis or osteoarthritis.. ANA testing should not be used to evaluate fatigue, back pain or other musculoskeletal pain unless accompanied by one or more of the clinical features listed in Recommendation 2.. RECOMMENDATION 2: ANA testing indicated. ANA testing is a useful diagnostic adjunct if the clinical history and physical examination show symptoms and signs of CTD ...
Ana Paula Pereira Velosa, Michelle Abdo Paiva, Priscila Cristina Andrade, Romy Beatriz Christmann, Esmeralda Miristeni Eher, Sandra Morais Fernezlian, Edwin Roger Parra, Walcy Rosolia Teodoro, Vera Luiza Capelozzi ...
CONCLUSIONS: Long-term post-transplant survival in Northern Spanish patients with CTD-ILD is reduced compared with IPF. PMID: 31694743 [PubMed - as supplied by publisher]...
Expert Team: Our team includes pulmonologists, rheumatologists, radiologists, pathologists, statisticians, nurses and staff members, who are all dedicated to improving your health care.
The present study shows that survival in patients with PAH is influenced by several factors. Although highly relevant baseline clinical characteristics are strong determinants of outcome, estimation of survival is also subject to several biases, including presence of associated conditions and interval from diagnosis to study enrolment. This strongly suggests that analysis of incident cohorts of homogeneous PAH populations should be recommended in future survival studies.. As previously described, associated conditions may dramatically influence survival rates in PAH cohorts 5-14. Our results confirm that patients with PAH complicating the course of congenital heart disease are more likely to survive to 3 yrs compared to patients that develop PAH in the setting of connective tissue diseases, such as systemic sclerosis, despite similar management approaches 5, 9, 10. Therefore, we recommend that PAH cases with associated conditions (e.g. connective tissue disease, portal hypertension, HIV ...
Diseases of the lung are classified as obstructive lung diseases like chronic obstructive pulmonary disease or cystic fibrosis, and restrictive lung diseases.
In an effort to understand the reasons behind people of any age, including children, being struck down with Rheumatoid Arthritis (RA) and other connective tissue diseases, we have delved and found some valuable and exciting conventional medical research.. The book The New Arthritis Breakthrough chronicles some 50 years of research and successful treatment of over 10,000 patients by the eminent US doctor Thomas McPherson Brown. It cites clinical trials that have repeatedly shown the link between bacteria and the inflammatory process that causes RA and other connective tissue diseases. Trial results show how these debilitating conditions are responsive to low dose antibiotic therapy. Patient reports in the book tell how antibiotic therapy has allowed them to discontinue cortisone, anti inflammatories and immuno-suppressant medications and regain a normal life after years of pain, debility, surgery, unemployment and untold difficulty.. In addition to results that are thought impossible for ...
Case 2 had a number of features which are more closely associated with SLE. Firstly, there was a history of sun exposure. In this context, it is noteworthy that anti-Ro and anti-La antibodies, which were positive in this patient, are particularly associated with photosensitivity (Sontheimer et al. 1979). One model of the pathogenesis of photosensitivity in SLE proposes that exposure of keratinocytes to ultraviolet light increases the surface expression of Ro antigen. Anti-Ro antibodies would then bind these receptors and precipitate a cutaneous reaction which then begets a systemic reaction (Furukawa et al. 1999). It is tempting to speculate that such a mechanism may have triggered the final illness in Case 2, but this cannot be known for certain. This case showed vascular thrombosis in the affected lymph nodes, a feature which is seen in SLE.. Case 2 also showed focal evidence of haemophagocytosis in the lymph nodes. This was an interesting observation, but one whose significance is uncertain. ...
Welcome to the Rheumatology Department at North Devon District Hospital. We provide high quality care to patients with connective tissue diseases such as rheumatoid arthritis, ankylosing spondylitis, psoriatic arthritis and many more.. We are a multidisciplinary team comprising of two rheumatology consultants and four clinical nurse specialists, as well as physiotherapists, occupational therapists and many other staff who support the department (around 20 staff in all).. We treat over 3000 patients across the North Devon area with connective tissue diseases. We run clinics in North Devon District Hospital as well as satellite community clinics in Bideford and South Molton.. Use the links on the left to find out more about the services we offer or access patient information about conditions and medications.. ...
Lesley Ann Saketkoo, Shikha Mittoo, Dörte Huscher, Dinesh Khanna, Paul F Dellaripa, Oliver Distler, Kevin R Flaherty, Sid Frankel, Chester V Oddis, Christopher P Denton, Aryeh Fischer, Otylia M Kowal-Bielecka, Daphne LeSage, Peter A Merkel, Kristine Phillips, David Pittrow, Jeffrey Swigris, Katerina Antoniou, Robert P Baughman, Flavia V Castelino, Romy B Christmann, Lisa Christopher-Stine, Harold R Collard, Vincent Cottin, Sonye Danoff, Kristin B Highland, Laura Hummers, Ami A Shah, Dong Soon Kim, David A Lynch, Frederick W Miller, Susanna M Proudman, Luca Richeldi, Jay H Ryu, Nora Sandorfi, Catherine Sarver, Athol U Wells, Vibeke Strand, Eric L Matteson, Kevin K Brown, James R Seibold ...
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心包填塞常見的病因包含癌症、腎衰竭、胸腔損傷(英语:chest trauma)和心包炎[2]。其他病因包括結締組織病(英语:connective tissue disease)、甲狀腺機能低下、主動脈破裂(英语:aortic rupture)和心臟外科手術[4]。在非洲,結核病是相對常見的病因[1]。 診斷時若出現低血壓、頸靜脈擴張(英语:jugular venous distension)、心包摩擦音(英语:pericardial rub),或心音較弱,則可能懷疑為心包填塞[2][1]。可由心電圖、胸腔X光攝影(英语:Chest radiograph)或心臟超音波佐證[2]。如果液體累積的速度較慢,心包可以擴張至容納超過兩公升液體;然而,若累積速度較快,約200毫升液體即可引發心包填塞[2]。 當心包填塞引起症狀時則需要進行引流[5]。引流方法包含心包穿刺術(英语:pericardiocentesis)、心包開窗術(英语:pericardial ...
P1: Possibility when comparing CTD-ILD group and UCTD-ILD group. P2: Possibility when comparing CTD-ILD group and IPF group. P3: Possibility when comparing UCTD-ILD group and IPF group ...
There are complex interactions between connective tissue disease (CTD) and interstitial lung disease (ILD), particularly in the PH patient. Clinicians that care for these patients will benefit from a deeper understanding of CTD and the ILD aspects of this diverse spectrum of disease. There are many clinical dilemmas to address and this course will focus on an approach to the evaluation and management of CTD-associated ILD.
From BioPortfolio: Interstitial lung disease (ILD) is a major pulmonary manifestation of connective tissue disease (CTD), leading to significant morbidity and mortality. Chest hig...
FIDIS (BMD, France) is a multiplex analytical flow cytometry system for the detection of antibodies. The aim of this study was to evaluate the FIDIS connective assay system for the detection of antinuclear antibodies (ANA), and to assess the clinical utility of these parameters in the diagnosis of connective tissue diseases. The FIDIS system simultaneously measures IgG antibodies directed at dsDNA, Ro, La, RNP, Sm, Jo-1, Scl-70, rRNP, and CENP-B. ...
Ehlers-Danlos Syndrome is a connective tissue disease, affecting collagen. Joints are very flexible and skin is loose and fragile.
Frequently Asked Questions (FAQs) on rheumatic diseases such as connective tissue diseases, vasculitis, arthritis, osteoarthritis, fibromyalgia, spondylitis, and more
As noted in this review, PH may be idiopathic or have disease associations (connective tissue diseases, congenital heart diseases, portal hypertension, HIV infection, drugs) and be associated with pulmonary diseases including COPD, although it is sometimes unclear in the latter case whether it is due to hemodynamic effects of the lung disease itself or overlap with another disorder of the pulmonary vasculature. ...
Objective. To evaluate plasma markers of endothelial cell activity in patients with pulmonary arterial hypertension (PAH) induced by connective tissue diseases (CTD) before and after 3-month administration of bosentan.. Methods. We quantified E, L and P-selectin (sE-S, sL-S, sP-S), thrombomodulin (TM), monocyte-chemotactic protein 1 (MCP-1), human soluble CD40 ligand (sCD40L), and nitric oxide (NO) in 18 patients and 18 controls. We evaluated right ventricular systolic pressure (RVSP) and the 6-minute walk test (6-MWT).. Results. All plasma markers but sL-S and TM at Time 0 were significantly higher in patients compared with controls. After 3 months of therapy, decreased levels were noted in NO (Time 0 24.05 ± 6.01 mmol/l, Time 1 13.92 ± 3.40 mmol/l; p , 0.001) and sCD40L (Time 0 1685.33 ± 866 pg/ml, Time 1 1055.11 ± 630.6 pg/ml; p = 0.017). In contrast, sP-S was significantly increased (Time 0 88.36 ± 47.76 ng/ml, Time 1 147.21 ± 94.43 ng/ml; p = 0.021). All patients remained stable in ...
Carver stood in four general elections for UKIP: Orpington in 1997 (5th, 526 votes), Cheltenham in 2001 (6th, 482 votes), Preseli Pembrokeshire in 2005 (5th, 498 votes), and Stourbridge in 2015 (3rd, 7,774 votes). He was also sixth on the party list for London in the 1999 European election.. Carver is of Romanichal descent on his grandmothers side, giving rise to his interest in fostering better relationships with traveller communities.[4] He believes that he is the only British Parliamentarian from a Romany background.[4] He has also helped raise both money and awareness for the Scleroderma Society following the death of his first wife from scleroderma in 2009.[5] He has a lifelong commitment to raise awareness of this relatively unknown connective tissue disease.[5]. In April 2017, Carver resigned as UKIPs foreign affairs spokesperson following the partys promise to ban the wearing of the burqa in public. He said that no one has the right to dictate what people should wear, and that the ...
Diagnosing SS is complicated by the range of symptoms a patient may manifest, and the similarity between symptoms of SS and those of other conditions. Also, patients who have symptoms of SS approach different specialities regarding their symptoms which make the diagnosis difficult. Since the symptoms of this autoimmune disorder such as dry eyes and dry mouth are very common among people, and mostly observed from the age of 40 and above, it is often mistaken as age-related, thus ignored. However, some medications can also cause symptoms that are similar to those of SS. The combination of several tests, which can be done in a series, can eventually lead to the diagnosis of SS.[16][34]. SS is usually classified as either primary or secondary. Primary Sjögren syndrome occurs by itself and secondary Sjögren syndrome occurs when another connective tissue disease is present.. Blood tests can be done to determine if a patient has high levels of antibodies that are indicative of the condition, such ...
Our clinical team plays an important preventative role by identifying those who might be at risk for osteoporosis as well as by building greater awareness of the need for early diagnosis and treatment. An important procedure for identifying those at risk for osteoporosis, or those who already have the disease, is through bone density testing. We do read these test in our clinic and then give our recommendation in terms of treatment. Consultation and treatment of chronic pain conditions (back/neck, hand/foot pain and other joint pain) is part of our routine work in this clinic.. Joint Aspirations and joint injections (for shoulders, elbows, wrists, hands, knees, ankles, and feet are performed in this clinic.. Specialist diagnostic and treatment services for patients with all forms of rheumatic complaints including connective tissue diseases, inflammatory arthritis, osteoarthritis, and orthopedic medical conditions.. ...
Introduction Some patients belong to clinical group 1 of the pulmonary hypertension classification but their underlying conditions are different, and they require a different management strategy. These include children who present with PAH, and those with underlying connective tissue disease or congenital heart de ...
Laura, Im sorry to hear about the fatigue. I dont take Cellcept, but Im guessing it might be hard to tell the difference sometimes if the fatigue is due to a med or if its due to the connective tissue disease. I wish I had an easy answer about the fatigue. Aside from my multivitamin and calcium, I dont take anything. I took fish oil for a while because its supposed to be good for inflamation, but it didnt st well in my stomach. For me, the thing that has helped my fatigue the most has been prednisone. I still have fatigue but its more manageable. Hopefully someone who takes cellcept will see your post and be able to give you more info about it ...
[Anorectal manifestations in systemic diseases]. Rev Med Interne. 2019 Aug 07;: Authors: Egal A, London J, Lidove O, Atienza P, Etienney I Abstract Numerous systemic diseases (vasculitis, connective tissue disease or sarcoidosis) can display an involvement of the perianal skin, the rectum and/or the anus. Such knowledge is important in order to treat these complications specif...
I never in a million years thought this would work on diabetes!!. I have had diabetes since 2005 taking Metformin and Glipizide twice a day. My diabetes has mainly been under control (unless I get out of control with my food). All these years I have been under the impression that I couldnt have corn, peas, bananas, watermelon, rice, pasta, bread - all because of the sugar. So when I say my diabetes gets out of control, its because I eat these things and not a little of it.. Meet Dr. McDougall (drmcdougall.com). This doctor has been treated diabetics for over 30 years. I recently learned of him when my daughter was diagnosed with some kind of connective tissue disease and she didnt want to take the medication (which was for lupus, etc.). She found Dr. McDougalls website and began using his regimen. In the first week, the pain in her legs went away (she could barely walk from the edema in her feet and legs) and her arms and hands are subsiding in pain as well. She is not diabetic. She has ...
The news I got is not pretty or happy or pleasant, not by any stretch of the imagination. The hypermobility, there is no treatment or cure other than palliative care, meaning that my excruciating, unmitigated pain will continue without cease or relief, most likely for the rest of my life. Not only that, but it comes with joint slippage and dislocations. Definitely debilitating. Then you have the connective tissue disease and the arthritis, both of which include pain of their own but can be treated. However, there is a distinct possibility of degeneration in time, especially with the arthritis, which is debilitating as well even if the pain is alleviated. It would be nice to have some of the pain taken care of and taken away, even if not all can be. All that, on top of the Hashimotos and Addisons that must be closely managed if Im to live normally or stay alive at all, the food allergies and IBS that can make my life a living hell in the blink of an eye and last for weeks at a time, depression ...
Inflammation normally presents a rapid loss of vision. Colour vision is frequently affected. Occasionally inflammation of the optic nerve may cause pain behind the eyes, especially during eye movements. A diagnosis can usually be made on clinical grounds alone. However, because inflammation is often related to diseases that can affect other parts of the body, such as connective tissue disease and multiple sclerosis, some blood investigations and an MRI may be necessary. Treatment with steroids may be required ...
Proteinuria may be an early indicator of renal disease and increases the risk of renal impairment, hypertension, and cardiovascular disease. Exclude causes of transient proteinuria (box), which does not have these associations. If proteinuria of 1+ or more persists on two subsequent dipstick tests at weekly intervals further investigation is indicated.. History-Ask about symptoms of renal failure and connective tissue diseases (including arthralgia, mouth ulcers, and rashes). Pertinent past medical history … ...
Recently my colleague received a referral from a certain unit with an ill patient hooked up on oxygen, as the lung function was pretty much not doing her much justice in the area of gas exchange, due to a fair amount of pulmonary haemorrhage aka bleeding in the lungs, clearly shown in the chest signs and radiograph. Her stare with the bloodshot Dracula eyes with florid conjunctiva haemorrhage were hardly a sign of terror, but simply the horrible sad, gloomy subsets of the aftermath of the probable over-the-top anticoagulation disorder coupled with her underlying connective tissue disease. ...