Hyperostosis: Increase in the mass of bone per unit volume.Hyperostosis, Diffuse Idiopathic Skeletal: A disease of elderly men characterized by large osteophytes that bridge vertebrae and ossification of ligaments and tendon insertions.Acquired Hyperostosis Syndrome: Syndrome consisting of SYNOVITIS; ACNE CONGLOBATA; PALMOPLANTAR PUSTULOSIS; HYPEROSTOSIS; and OSTEITIS. The most common site of the disease is the upper anterior chest wall, characterized by predominantly osteosclerotic lesions, hyperostosis, and arthritis of the adjacent joints. The association of sterile inflammatory bone lesions and neutrophilic skin eruptions is indicative of this syndrome.Hyperostosis Frontalis Interna: Thickening of the inner table of the frontal bone, which may be associated with hypertrichosis and obesity. It most commonly affects women near menopause.Hyperostosis, Sternocostoclavicular: A rare, benign rheumatologic disorder or syndrome characterized by hyperostosis and soft tissue ossification between the clavicles and the anterior part of the upper ribs. It is often associated with the dermatologic disorder palmoplantar pustulosis, particularly in Japan. Careful diagnosis is required to distinguish it from psoriatic arthritis, OSTEITIS DEFORMANS, and other diseases. Spondylitis of pustulosis palmaris et plantaris is one of the possible causes; also, evidence suggests one origin may be bone infection. Bone imaging is especially useful for diagnosis. It was originally described by Sonozaki in 1974.Exostoses: Benign hypertrophy that projects outward from the surface of bone, often containing a cartilaginous component.Melorheostosis: A form of osteosclerosis extending in a linear track mainly through one of the long bones of the upper and lower limbs.Ankylosis: Fixation and immobility of a joint.Paleopathology: The study of disease in prehistoric times as revealed in bones, mummies, and archaeologic artifacts.Papilloma, Inverted: A mucosal tumor of the urinary bladder or nasal cavity in which proliferating epithelium is invaginated beneath the surface and is more smoothly rounded than in other papillomas. (Stedman, 25th ed)Osteitis: Inflammation of the bone.Hyperostosis, Cortical, Congenital: A disease of young infants characterized by soft tissue swellings over the affected bones, fever, and irritability, and marked by periods of remission and exacerbation. (Dorland, 27th ed)Spinal Osteophytosis: Outgrowth of immature bony processes or bone spurs (OSTEOPHYTE) from the VERTEBRAE, reflecting the presence of degenerative disease and calcification. It commonly occurs in cervical and lumbar SPONDYLOSIS.Paranasal Sinuses: Air-filled spaces located within the bones around the NASAL CAVITY. They are extensions of the nasal cavity and lined by the ciliated NASAL MUCOSA. Each sinus is named for the cranial bone in which it is located, such as the ETHMOID SINUS; the FRONTAL SINUS; the MAXILLARY SINUS; and the SPHENOID SINUS.Skull: The SKELETON of the HEAD including the FACIAL BONES and the bones enclosing the BRAIN.Cervical Vertebrae: The first seven VERTEBRAE of the SPINAL COLUMN, which correspond to the VERTEBRAE of the NECK.Meningioma: A relatively common neoplasm of the CENTRAL NERVOUS SYSTEM that arises from arachnoidal cells. The majority are well differentiated vascular tumors which grow slowly and have a low potential to be invasive, although malignant subtypes occur. Meningiomas have a predilection to arise from the parasagittal region, cerebral convexity, sphenoidal ridge, olfactory groove, and SPINAL CANAL. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2056-7)Bone Diseases, DevelopmentalFibula: The bone of the lower leg lateral to and smaller than the tibia. In proportion to its length, it is the most slender of the long bones.Spinal DiseasesParanasal Sinus Neoplasms: Tumors or cancer of the PARANASAL SINUSES.Sternum: A long, narrow, and flat bone commonly known as BREASTBONE occurring in the midsection of the anterior thoracic segment or chest region, which stabilizes the rib cage and serves as the point of origin for several muscles that move the arms, head, and neck.Longitudinal Ligaments: Two extensive fibrous bands running the length of the vertebral column. The anterior longitudinal ligament (ligamentum longitudinale anterius; lacertus medius) interconnects the anterior surfaces of the vertebral bodies; the posterior longitudinal ligament (ligamentum longitudinale posterius) interconnects the posterior surfaces. The commonest clinical consideration is OSSIFICATION OF POSTERIOR LONGITUDINAL LIGAMENT. (From Stedman, 25th ed)Meningeal Neoplasms: Benign and malignant neoplastic processes that arise from or secondarily involve the meningeal coverings of the brain and spinal cord.Skull Base Neoplasms: Neoplasms of the base of the skull specifically, differentiated from neoplasms of unspecified sites or bones of the skull (SKULL NEOPLASMS).Nose Neoplasms: Tumors or cancer of the NOSE.Bone and Bones: A specialized CONNECTIVE TISSUE that is the main constituent of the SKELETON. The principle cellular component of bone is comprised of OSTEOBLASTS; OSTEOCYTES; and OSTEOCLASTS, while FIBRILLAR COLLAGENS and hydroxyapatite crystals form the BONE MATRIX.Tomography, X-Ray Computed: Tomography using x-ray transmission and a computer algorithm to reconstruct the image.Sternoclavicular Joint: A double gliding joint formed by the CLAVICLE, superior and lateral parts of the manubrium sterni at the clavicular notch, and the cartilage of the first rib.Sternocostal Joints: An articulation where the costal cartilage of each rib fit with slight concavities along the lateral borders of the STERNUM.Hidradenitis Suppurativa: A chronic suppurative and cicatricial disease of the apocrine glands occurring chiefly in the axillae in women and in the groin and anal regions in men. It is characterized by poral occlusion with secondary bacterial infection, evolving into abscesses which eventually rupture. As the disease becomes chronic, ulcers appear, sinus tracts enlarge, fistulas develop, and fibrosis and scarring become evident.Mast Cells: Granulated cells that are found in almost all tissues, most abundantly in the skin and the gastrointestinal tract. Like the BASOPHILS, mast cells contain large amounts of HISTAMINE and HEPARIN. Unlike basophils, mast cells normally remain in the tissues and do not circulate in the blood. Mast cells, derived from the bone marrow stem cells, are regulated by the STEM CELL FACTOR.Sweat Gland Diseases: Diseases of the SWEAT GLANDS.Acne Vulgaris: A chronic disorder of the pilosebaceous apparatus associated with an increase in sebum secretion. It is characterized by open comedones (blackheads), closed comedones (whiteheads), and pustular nodules. The cause is unknown, but heredity and age are predisposing factors.ArchivesBiological Science Disciplines: All of the divisions of the natural sciences dealing with the various aspects of the phenomena of life and vital processes. The concept includes anatomy and physiology, biochemistry and biophysics, and the biology of animals, plants, and microorganisms. It should be differentiated from BIOLOGY, one of its subdivisions, concerned specifically with the origin and life processes of living organisms.Periodicals as Topic: A publication issued at stated, more or less regular, intervals.PubMed: A bibliographic database that includes MEDLINE as its primary subset. It is produced by the National Center for Biotechnology Information (NCBI), part of the NATIONAL LIBRARY OF MEDICINE. PubMed, which is searchable through NLM's Web site, also includes access to additional citations to selected life sciences journals not in MEDLINE, and links to other resources such as the full-text of articles at participating publishers' Web sites, NCBI's molecular biology databases, and PubMed Central.Dystonia Musculorum Deformans: A condition characterized by focal DYSTONIA that progresses to involuntary spasmodic contractions of the muscles of the legs, trunk, arms, and face. The hands are often spared, however, sustained axial and limb contractions may lead to a state where the body is grossly contorted. Onset is usually in the first or second decade. Familial patterns of inheritance, primarily autosomal dominant with incomplete penetrance, have been identified. (Adams et al., Principles of Neurology, 6th ed, p1078)Osteitis Deformans: A disease marked by repeated episodes of increased bone resorption followed by excessive attempts at repair, resulting in weakened, deformed bones of increased mass. The resultant architecture of the bone assumes a mosaic pattern in which the fibers take on a haphazard pattern instead of the normal parallel symmetry.Spondylosis: A degenerative spinal disease that can involve any part of the VERTEBRA, the INTERVERTEBRAL DISK, and the surrounding soft tissue.Hernia: Protrusion of tissue, structure, or part of an organ through the bone, muscular tissue, or the membrane by which it is normally contained. Hernia may involve tissues such as the ABDOMINAL WALL or the respiratory DIAPHRAGM. Hernias may be internal, external, congenital, or acquired.OsteomyelitisRecurrence: The return of a sign, symptom, or disease after a remission.Chronic Disease: Diseases which have one or more of the following characteristics: they are permanent, leave residual disability, are caused by nonreversible pathological alteration, require special training of the patient for rehabilitation, or may be expected to require a long period of supervision, observation, or care. (Dictionary of Health Services Management, 2d ed)International Classification of Diseases: A system of categories to which morbid entries are assigned according to established criteria. Included is the entire range of conditions in a manageable number of categories, grouped to facilitate mortality reporting. It is produced by the World Health Organization (From ICD-10, p1). The Clinical Modifications, produced by the UNITED STATES DEPT. OF HEALTH AND HUMAN SERVICES, are larger extensions used for morbidity and general epidemiological purposes, primarily in the U.S.Databases, Factual: Extensive collections, reputedly complete, of facts and data garnered from material of a specialized subject area and made available for analysis and application. The collection can be automated by various contemporary methods for retrieval. The concept should be differentiated from DATABASES, BIBLIOGRAPHIC which is restricted to collections of bibliographic references.Osteosclerosis: An abnormal hardening or increased density of bone tissue.Acute Generalized Exanthematous Pustulosis: Rare skin eruption characterized by acute formation of pustules filled with NEUTROPHILS, fever, and peripheral blood LEUKOCYTOSIS. Most cases are associated with the use of antibiotics (e.g., BETA-LACTAMS).Hong Kong: The former British crown colony located off the southeast coast of China, comprised of Hong Kong Island, Kowloon Peninsula, and New Territories. The three sites were ceded to the British by the Chinese respectively in 1841, 1860, and 1898. Hong Kong reverted to China in July 1997. The name represents the Cantonese pronunciation of the Chinese xianggang, fragrant port, from xiang, perfume and gang, port or harbor, with reference to its currents sweetened by fresh water from a river west of it.Osteoblasts: Bone-forming cells which secrete an EXTRACELLULAR MATRIX. HYDROXYAPATITE crystals are then deposited into the matrix to form bone.
A case report of synovitis, acne, pustulosis, hyperostosis and osteitis syndrome presenting with spondylodiscitis. (1/60)
SAPHO syndrome stands for synovitis, acne, pustulosis, hyperostosis and osteitis. The common site of skeletal lesions in this syndrome is the sternocostoclavicular area. Spondylodiscitis is rarely described in published studies. In general, skin lesions develop before the onset of skeletal lesions. We report a case of SAPHO syndrome in which spondylodiscitis developed more than 1 year before the onset of pustulosis. (+info)Proximal femoral bone loss and increased rate of fracture with a proximally hydroxyapatite-coated femoral component. (2/60)
We performed a retrospective analysis of the clinical and radiological outcomes of total hip replacement using an uncemented femoral component proximally coated with hydroxyapatite. Of 136 patients, 118 who had undergone 124 primary total hip replacements were available for study. Their mean age was 66.5 years (19 to 90) and the mean follow-up was 5.6 years (4.25 to 7.25). At the final follow-up the mean Harris hip score was 92 (47.7 to 100). Periprosthetic femoral fractures, which occurred in seven patients (5.6%), were treated by osteosynthesis in six and conservatively in one. We had to revise five femoral components, one because of aseptic loosening, one because of septic loosening and three because of periprosthetic fracture. At the final follow-up there were definite signs of aseptic loosening in two patients. Radiologically, proximal femoral bone loss in Gruen zones I and VI was evident in 96.8% of hips, while bone hypertrophy in zones III and V was seen in 64.7%. In 24 hips (20.2%) the mean subsidence of the stem was 3.7 mm which occurred within the first 12 postoperative weeks. This indicated poor initial stability, which might have been aggravated by early weight-bearing. The high rate of failure in our study suggests that proximal femoral bone loss affects the long-term survival of the replacement. (+info)Hypertrophic osteodystrophy in a Great Dane puppy. (3/60)
An intact male, Great Dane puppy was evaluated for weakness, lethargy, reluctance to move, and inability to stand. Hypertrophic osteodystrophy was diagnosed based on clinical and radiographic findings. Clinical signs, radiographic lesions, gross pathology, histopathology, etiology, and treatment of the disease are discussed. (+info)Stenosis of the cervical canal in craniodiaphyseal dysplasia. (4/60)
Craniodiaphyseal dysplasia (CDD) is a rare sclerosing bone disorder, the severity of which depends on its phenotypic expression. Hyperostosis can cause progressive foraminal stenosis leading to palsy of cranial nerves, epilepsy and mental retardation. We report the only case of CDD in an adult, with stenosis of the cervical canal leading to quadriparesis as a late complication of hyperostosis, and describe the problems associated with its treatment. Although the syndrome is rare, its pathophysiological and therapeutic considerations may be applicable to the management of stenosis of the spinal canal in other hyperostotic bone disorders. (+info)Frequency variations of discrete cranial traits in major human populations. III. Hyperostotic variations. (5/60)
Seven discrete cranial traits usually categorised as hyperostotic characters, the medial palatine canal, hypoglossal canal bridging, precondylar tubercle, condylus tertius, jugular foramen bridging, auditory exostosis, and mylohyoid bridging were investigated in 81 major human population samples from around the world. Significant asymmetric occurrences of the bilateral traits were detected in the medial palatine canal and jugular foramen bridging in several samples. Significant intertrait associations were found between some pairs of the traits, but not consistently across the large geographical samples. The auditory exostosis showed a predominant occurrence in males. With the exception of the auditory exostosis and mylohyoid bridging in a few samples, significant sex differences were slight. The frequency distributions of the traits (except for the auditory exostosis) showed some interregional clinality and intraregional discontinuity, suggesting that genetic drift could have contributed to the observed pattern of variation. (+info)Simultaneous reduction in cancer pain, bone destruction, and tumor growth by selective inhibition of cyclooxygenase-2. (6/60)
More than half of all chronic cancer pain arises from metastases to bone, and bone cancer pain is one of the most difficult of all persistent pain states to fully control. Several tumor types including sarcomas and breast, prostate, and lung carcinomas grow in or preferentially metastasize to the skeleton where they proliferate, and induce significant bone remodeling, bone destruction, and cancer pain. Many of these tumors express the isoenzyme cycloxygenase-2 (COX-2), which is involved in the synthesis of prostaglandins. To begin to define the role COX-2 plays in driving bone cancer pain, we used an in vivo model where murine osteolytic 2472 sarcoma cells were injected and confined to the intramedullary space of the femur in male C3HHeJ mice. After tumor implantation, mice develop ongoing and movement-evoked bone cancer pain-related behaviors, extensive tumor-induced bone resorption, infiltration of the marrow space by tumor cells, and stereotypic neurochemical alterations in the spinal cord reflective of a persistent pain state. Thus, after injection of tumor cells, bone destruction is first evident at day 6, and pain-related behaviors are maximal at day 14. A selective COX-2 inhibitor was administered either acutely [NS398; 100 mg/kg, i.p.] on day 14 or chronically in chow [MF. tricyclic; 0.015%, p.o.] from day 6 to day 14 after tumor implantation. Acute administration of a selective COX-2 inhibitor attenuated both ongoing and movement-evoked bone cancer pain, whereas chronic inhibition of COX-2 significantly reduced ongoing and movement-evoked pain behaviors, and reduced tumor burden, osteoclastogenesis, and bone destruction by >50%. The present results suggest that chronic administration of a COX-2 inhibitor blocks prostaglandin synthesis at multiple sites, and may have significant clinical utility in the management of bone cancer and bone cancer pain. (+info)Vascular malformations of the lower limb with osseous involvement. (7/60)
Vascular malformations are rare congenital lesions which often have associated skeletal changes. Over a period of ten years, 90 patients at our clinic had a vascular anomaly of the lower limb, examined by either CT or MRI. Of these, 18 (20%) had bony involvement. A questionnaire was sent to these patients (8 men, 10 women) to evaluate their age of presentation, initial symptoms and current complaints. Radiological imaging revealed 15 low- and three high-flow lesions. The mean age at presentation to a physician was six years of age. Pain was the most common complaint. Disparity in leg length of 2 cm or more was observed in ten patients. Of the 16 patients with muscle infiltration, 13 had four or more muscles involved. Treatment by resection alone would require radical surgery. (+info)Genomic deletion of a long-range bone enhancer misregulates sclerostin in Van Buchem disease. (8/60)
Mutations in distant regulatory elements can have a negative impact on human development and health, yet because of the difficulty of detecting these critical sequences, we predominantly focus on coding sequences for diagnostic purposes. We have undertaken a comparative sequence-based approach to characterize a large noncoding region deleted in patients affected by Van Buchem (VB) disease, a severe sclerosing bone dysplasia. Using BAC recombination and transgenesis, we characterized the expression of human sclerostin (SOST) from normal (SOST(wt)) or Van Buchem (SOST(vbDelta) alleles. Only the SOST(wt) allele faithfully expressed high levels of human SOST in the adult bone and had an impact on bone metabolism, consistent with the model that the VB noncoding deletion removes a SOST-specific regulatory element. By exploiting cross-species sequence comparisons with in vitro and in vivo enhancer assays, we were able to identify a candidate enhancer element that drives human SOST expression in osteoblast-like cell lines in vitro and in the skeletal anlage of the embryonic day 14.5 (E14.5) mouse embryo, and discovered a novel function for sclerostin during limb development. Our approach represents a framework for characterizing distant regulatory elements associated with abnormal human phenotypes. (+info)
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![2020 ICD-10-CM Diagnosis Code M48.10: Ankylosing hyperostosis [Forestier], site unspecified](data:image/png;base64,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)
2020 ICD-10-CM Diagnosis Code M48.10: Ankylosing hyperostosis [Forestier], site unspecified
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Craniofacial bonesSyndromeIdiopathicSkeletalDISHCorticalFrontalis InternaPustulosisOsteitisSpineCorticalisBoneForestier'sDiseasePorotic hyperostosisVertebral hyperostosisEndosteal hyperostosisCalvarial hyperostosisSternocostoclavicularDefinitionSkeletal hyperostosisDiffuseFrontalis internaMeningiomaAcneCharacterized by benignArthritisSkullTreatmentHairResults
Craniofacial bones1
- Mutations in the pyrophosphate (PPi) transporter ANKH cause the autosomal dominant form of craniometaphyseal dysplasia (CMD), a rare disorder characterized by hyperostosis of craniofacial bones and widened metaphyses in long bones. (uconn.edu)
Syndrome3
- Acquired Hyperostosis Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings) . (uchicago.edu)
- This graph shows the total number of publications written about "Acquired Hyperostosis Syndrome" by people in this website by year, and whether "Acquired Hyperostosis Syndrome" was a major or minor topic of these publications. (uchicago.edu)
- Below are the most recent publications written about "Acquired Hyperostosis Syndrome" by people in Profiles. (uchicago.edu)
Idiopathic93
- Diffuse idiopathic skeletal hyperostosis Hyperostosis frontalis interna Infantile cortical hyperostosis Porotic hyperostosis SAPHO syndrome Stuart-Macadam P (April 1985). (wikipedia.org)
- Diffuse idiopathic skeletal hyperostosis (DISH) is a condition where the ligaments and tendons harden. (clevelandclinic.org)
- Diffuse idiopathic skeletal hyperostosis (DISH) is a skeletal disorder that causes ligaments and tendons in the body to calcify (harden). (clevelandclinic.org)
- What are the symptoms of diffuse idiopathic skeletal hyperostosis (DISH)? (clevelandclinic.org)
- What Facts Should I Know about Diffuse Idiopathic Skeletal Hyperostosis (DISH)? (emedicinehealth.com)
- Diffuse idiopathic skeletal hyperostosis (DISH) is a condition that causes bone to form in abnormal places. (emedicinehealth.com)
- How Is Diffuse Idiopathic Skeletal Hyperostosis Diagnosed ? (emedicinehealth.com)
- What Is the Treatment for Diffuse Idiopathic Skeletal Hyperostosis? (emedicinehealth.com)
- Diffuse Idiopathic Skeletal Hyperostosis (DISH) is a phenomenon that more commonly affects older males. (eorthopod.com)
- The most common finding of Diffuse Idiopathic Skeletal Hyperostosis (DISH) is ligaments that turn into bone. (eorthopod.com)
- These are the spinal ligaments that can turn into bone in Diffuse Idiopathic Skeletal Hyperostosis (DISH). (eorthopod.com)
- Diffuse Idiopathic Skeletal Hyperostosis generally occurs in people between the ages of 50 and 60. (eorthopod.com)
- Diffuse idiopathic skeletal hyperostosis (DISH) is a disorder in which there is bone growth in the ligaments, particularly where they attach to the bones of the spine. (uwhealth.org)
- All dogs were found to be affected with both disseminated idiopathic spinal hyperostosis and spondylosis deformans. (wiley.com)
- Neurological signs due to foraminal stenosis associated with disseminated idiopathic spinal hyperostosis were found in two dogs. (wiley.com)
- Differences between disseminated idiopathic spinal hyperostosis and spondylosis deformans found on magnetic resonance imaging contribute to an increased differentiation between the two entities. (wiley.com)
- We experienced 2 cases of spinal fracture in patients aged 80 years or older with diffuse idiopathic skeletal hyperostosis (DISH). (scirp.org)
- D. Resnick and G. Niwayama, "Radiographic and Pathologic Features of Spinal Involvement in Diffuse Idiopathic Skeletal Hyperostosis," Radiology, Vol. 119, 1976, pp. 559-568. (scirp.org)
- C. W. Denko and C. J. Malemud, "Body Mass Index and Blood Glucose: Correlations with Serum Insulin, Growth Hormone, and Insulin-Like Growth Factor-1 Levels in Patients with Diffuse Idiopathic Skeletal Hyperostosis (DISH)," Rheumatology International, Vol. 26, 2006, pp. 292-297. (scirp.org)
- Idiopathic hyperostosis of the calvaria in five young bullmastiffs. (semanticscholar.org)
- Study Design A retrospective review of 12 patients with ankylosing spondylitis (AS) and 18 patients with diffuse idiopathic skeletal hyperostosis (DISH) treated at a single institution for spinal injuries between the years 2000 and 2006. (ovid.com)
- Swallowing disorders due to diffuse idiopathic skeletal hyperostosis (DISH) often remain undetected, even if symptoms increase over the years. (minervamedica.it)
- Di Grezia G, Gatta G, Vecchione L, Vitiello G, D'Anna E, Dell'Aquila A. Computed tomography for the diagnosis and management of idiopathic cervical spine hyperostosis. (minervamedica.it)
- Diffuse Idiopathic Skeletal Hyperostosis (DISH) refers to a non-inflammatory disease that is characterized by ossification/calcification of soft tissues, entheses, and spinal ligaments. (physio-pedia.com)
- The reported prevalence of diffuse idiopathic skeletal hyperostosis is widely varied throughout the course of available research . (physio-pedia.com)
- Diffuse idiopathic skeletal hyperostosis (DISH) is a common disease of the aging population, characterized by multiple axial and extraaxial involvement. (asahq.org)
- Diffuse idiopathic skeletal hyperostosis (DISH) is a condition commonly affecting the spine characterized by calcification (bony hardening) of ligaments, tendons and joint capsule insertions. (fondren.com)
- Diffuse idiopathic skeletal hyperostosis is more common among individuals older than 50 years of age with a male predominance. (fondren.com)
- Diffuse idiopathic skeletal hyperostosis is often asymptomatic and is detected on unsuspected X-rays or CT/MRI scans. (fondren.com)
- Individuals with diffuse idiopathic skeletal hyperostosis tend to have a higher body mass index, elevated uric acid levels and a higher tendency to develop diabetes mellitus. (fondren.com)
- Diffuse idiopathic skeletal hyperostosis (DISH) is a non-inflammatory disease characterized by hyperostosis of the axial as well as peripheral skeleton. (prolekare.cz)
- In addition, the spinal column was affected by new bone formation along the vertebral bodies, bridging the disc spaces, as seen in diffuse idiopathic skeletal hyperostosis (DISH). (avmi.net)
- Diffuse idiopathic skeletal hyperostosis , or DISH, is considered a type of osteoarthritis that doesn't show any wear and tear, and may be present with no symptoms. (healthguideinfo.com)
- Whether testing for ankylosing spondylitis or diffuse idiopathic skeletal hyperostosis, your doctor will begin with a complete physical examination. (healthguideinfo.com)
- There is no known cure for ankylosing spondylitis or diffuse idiopathic skeletal hyperostosis, so treatment depends on the level of pain and involvement of the disease. (healthguideinfo.com)
- Diffuse idiopathic skeletal hyperostosis (DISH) is a form of degenerative arthritis characterized by excessive bone growth along the sides of the vertebrae of the spine. (diseaseinfosearch.org)
- Following organizations serve the condition "Diffuse idiopathic skeletal hyperostosis" for support, advocacy or research. (diseaseinfosearch.org)
- Finding the right clinical trial for Diffuse idiopathic skeletal hyperostosis can be challenging. (diseaseinfosearch.org)
- The terms "Diffuse idiopathic skeletal hyperostosis" returned 47 free, full-text research articles on human participants. (diseaseinfosearch.org)
- Morphological characteristics of diffuse idiopathic skeletal hyperostosis in the cervical spine. (diseaseinfosearch.org)
- Diffuse idiopathic skeletal hyperostosis (DISH) is characterized by anterior ossification of the spine and can lead to dysphagia and airway obstruction. (diseaseinfosearch.org)
- Diffuse idiopathic skeletal hyperostosis with cervical myelopathy. (diseaseinfosearch.org)
- Thoracic spondylolisthesis and spinal cord compression in diffuse idiopathic skeletal hyperostosis: a case report. (diseaseinfosearch.org)
- Diffuse idiopathic skeletal hyperostosis has long been regarded as a benign asymptomatic clinical entity with an innocuous clinical course. (diseaseinfosearch.org)
- Neurological complications are rare in diffuse idiopathic skeletal hyperostosis. (diseaseinfosearch.org)
- Fluoride Action Network Fluoride DISH Diffuse Idiopathic Skeletal Hyperostosis. (fungionline.org.uk)
- It is similar to diffuse idiopathic skeletal hyperostosis. (fungionline.org.uk)
- Home About Arthritis Types Diffuse Idiopathic Skeletal Hyperostosis. (fungionline.org.uk)
- Diffuse idiopathic skeletal hyperostosis DISH is a type of arthritis that affects tendons and ligaments, mainly around your spine. (fungionline.org.uk)
- Imaging Characteristics of Diffuse Idiopathic Skeletal Hyperostosis With an Emphasis on Acute Spinal Fractures: Review: American Journal of Roentgenology: Vol. 193, No. 3_supplement AJR. (fungionline.org.uk)
- 3A Absence of apophyseal joint ankylosis and costovertebral joint fusion with diffuse idiopathic skeletal hyperostosis, which is present with ankylosing spondylitis. (fungionline.org.uk)
- Axial CT image of thoracic spine in 66-year-old man with diffuse idiopathic skeletal hyperostosis shows normal apophyseal joints with no evidence of fusion long arrow and mild osteoarthritic changes of costovertebral joints that are not fused short arrow. (fungionline.org.uk)
- Rich table but short life: Diffuse idiopathic skeletal hyperostosis in Danish astronomer Tycho Brahe 1546-1601 and its possible consequences. (fungionline.org.uk)
- 2004 The prevalence of diffuse idiopathic skeletal hyperostosis in Korea. (fungionline.org.uk)
- Kiss C, O'Neill' TW, Mituszova M, Szilagyi M, Poór G 2002 The prevalence of diffuse idiopathic skeletal hyperostosis in a population-based study in Hungary. (fungionline.org.uk)
- Diffuse Idiopathic Skeletal Hyperostosis Involving Cervical and Lumbar Spine Presenting with Dysphagia: A Case Report. (fungionline.org.uk)
- Radiographic and pathological features of spinal involvement in diffuse idiopathic skeletal hyperostosis DISH Radiology. (fungionline.org.uk)
- Miyamoto K, Sugiyama S, Hosoe H, Iinuma N, Suzuki Y, etal Postsurgical recurrence of ost eophytes causing dysphagia in patients with diffuse idiopathic skeletal hyperostosis. (fungionline.org.uk)
- Keywords: Anterior Longitudinal Ligament, diffuse idiopathic skeletal hyperostosis, Forestier's' disease. (fungionline.org.uk)
- Diffuse idiopathic skeletal hyperostosis DISH Symptoms and causes Mayo Clinic. (fungionline.org.uk)
- Diffuse idiopathic skeletal hyperostosis DISH A common but less known cause of back pain. (fungionline.org.uk)
- Diffuse idiopathic skeletal hyperostosis DISH: Where we are now and where to go next. (fungionline.org.uk)
- Ankylosing vertebral hyperostosis HVA or diffuse idiopathic skeletal hyperostosis DISH is a disease often seen in the middle-aged and elderly, frequently in patients older than 70 years 10.1% in men, 6.8% in women. (fungionline.org.uk)
- Diffuse Idiopathic Skeletal Hyperostosis DISH Cleveland Clinic. (fungionline.org.uk)
- Diffuse idiopathic skeletal hyperostosis DISH is a systemic, relatively common condition, with an average prevalence of approximately 10% in people 50 years of age. (fungionline.org.uk)
- Diffuse Idiopathic Skeletal Hyperostosis is hardening, calcification of the spinal ligaments where they attach to bone , particularly at the front of the skeletal column. (docshay.com)
- Diffuse idiopathic skeletal hyperostosis (DISH) is basically calcification of ligaments along with hardening of bones in parts connected to spine. (drvikram.com)
- Diffuse idiopathic skeletal hyperostosis actually has no symptoms. (drvikram.com)
- Retinoids, like isotretinoin ,Amnesteem and Claravis increase the risk of diffuse idiopathic skeletal hyperostosis. (drvikram.com)
- Diffuse idiopathic skeletal hyperostosis if not treated can cause life-long complications. (drvikram.com)
- Obesity caused due to Diffuse idiopathic skeletal hyperostosis might lead to long term complications. (drvikram.com)
- Herbal Remedies for Ayurvedic Treatment of Diffuse Idiopathic Skeletal Hyperostosis , from Planet Ayurveda house are very effective. (drvikram.com)
- Diffuse idiopathic skeletal hyperostosis (DISH) is a condition that commonly affects the spine. (atlspinesurgery.com)
- We're all familiar with the spinal findings of diffuse idiopathic skeletal hyperostosis (DISH). (xraymachines.info)
- Diffuse idiopathic skeletal hyperostosis (DISH): Forestier's disease with extraspinal manifestations. (xraymachines.info)
- Diffuse idiopathic skeletal hyperostosis (DISH) is not really an arthropathy because it spares synovium, articular cartilage, and articular osseous surfaces. (dieutridau.com)
- Diffuse idiopathic skeletal hyperostosis (DISH) is associated with more cardiovascular events than is predicted by the Framingham Risk Score (FRS). (mdedge.com)
- D iffuse idiopathic skeletal hyperostosis (DISH) is a disorder affecting both the vertebral column and the extra-axial skeleton, and is characterized by ossification of ligaments, with hyperostosis at their points of attachment to bone. (thejns.org)
- Diffuse idiopathic skeletal hyperostosis (DISH) -- also called Forestier's disease -- is considered to be a form of Osteoarthritis or degenerative arthritis. (alwaysayurveda.net)
- Diffuse idiopathic skeletal hyperostosis is a condition which implies a bony hardening (calcification) of ligaments at the points at which they are attached to the spine. (alwaysayurveda.net)
- Diffuse idiopathic skeletal hyperostosis is generally linked to tendinitis (inflammation) and calcification of tendons at the point of their attachment to the bone. (alwaysayurveda.net)
- The exact cause behind the occurrence of Diffuse idiopathic skeletal hyperostosis is not known. (alwaysayurveda.net)
- The standard treatment for Diffuse idiopathic skeletal hyperostosis involves the use of anti-inflammatory medications because the condition typically leads to the inflammation of the areas of the spine and tendons. (alwaysayurveda.net)
- Some excellent herbal formulations offered by Planet Ayurveda herbal manufacturing company can be very useful in managing the symptoms of Diffuse idiopathic skeletal hyperostosis. (alwaysayurveda.net)
- The use of these capsules can reduce inflammation, provide relief from pain, and manage other symptoms associated with Diffuse idiopathic skeletal hyperostosis. (alwaysayurveda.net)
- Recommended dosage of Boswellia Curcumin capsules for managing the symptoms of Diffuse idiopathic skeletal hyperostosis: 1 capsules with plain water, two times a day, after meals. (alwaysayurveda.net)
- Although cervical anterior osteophytes accompanying diffuse idiopathic skeletal hyperostosis (DISH) are generally asymptomatic, large osteophytes sometimes cause swallowing disorders. (europeanspinejournal.org)
- Physical examination and radiography revealed signs consistent with diffuse idiopathic skeletal hyperostosis (DISH), including a C7-T1 osteophyte causing severe tracheal compression. (thejns.org)
- Diffuse idiopathic skeletal hyperostosis describes a widespread condition of unknown cause that causes excessive, abnormal bone growth in the human skeleton. (cure-back-pain.org)
- Tanishima S, Takeda C, Hamamoto Y, Kondo Y, Nagashima H. Prompt surgical management for spinal fracture in the elderly aged over 90 years with diffuse idiopathic skeletal hyperostosis to extend their healthy lifespan. (springer.com)
- The prevalence of diffuse idiopathic skeletal hyperostosis (DISH) in two large American Midwest metropolitan hospital populations. (springer.com)
- Baxi V, Gaiwal S. Diffuse idiopathic skeletal hyperostosis of cervical spine-an unusual cause of difficult flexible fiber optic intubation. (springer.com)
- Diffuse idiopathic skeletal hyperostosis (DISH or Forestier's disease) is a form of degenerative arthritis. (medicinenet.com)
Skeletal4
- Porosities in the outer table of the cranial vault (porotic hyperostosis) and orbital roof (cribra orbitalia) are among the most frequent pathological lesions seen in ancient human skeletal collections. (nih.gov)
- Infantile cortical hyperostosis (ICH), Caffey disease, is a multifocal, inflammatory skeletal process with classic onset before the fifth month of life and resolution by the age of 3 years. (semanticscholar.org)
- Our study shows that hyperostosis of the spine and peripheral skeletal parts occurs more frequently among fluoride-exposed aluminum smelter workers. (fungionline.org.uk)
- Camurati-Engelmann disease is a skeletal condition that is characterized by abnormally thick bones (hyperostosis) in the arms, legs, and skull. (medlineplus.gov)
DISH2
- DISH is also known as Forestier's disease, spondylitis ossificans ligamentosa, spondylosis hyperostotica, and ankylosing hyperostosis of the spine. (emedicinehealth.com)
- Despite its old characterisation previously described as ankylosing hyperostosis by Forestier and Rotes-Querol, 1 DISH is still insufficiently investigated and understood. (fungionline.org.uk)
Cortical31
- In 1945, Caffey first described infantile cortical hyperostosis (Caffey disease), a self-limited disorder that affects infants and causes bone changes, soft-tissue swelling, and irritability. (medscape.com)
- Infantile cortical hyperostosis is an inflammatory process of unclear etiology. (medscape.com)
- Bone mineral density (BMD) was normal in adult patients of both families who had had an episode of cortical hyperostosis, regardless of the presence or absence of the p.Arg1014Cys mutation. (medscape.com)
- Infantile cortical hyperostosis has been reported to affect 3 of 1000 infants younger than age 6 months. (medscape.com)
- [ 3 , 20 ] The average age at onset for the sporadic form of infantile cortical hyperostosis is 9-11 weeks. (medscape.com)
- Infantile cortical hyperostosis usually runs its course and resolves without sequelae in 6-9 months. (medscape.com)
- [ 21 ] These symptoms were similar to symptoms present at the age of 1 month, at which time she was diagnosed as having cortical hyperostosis. (medscape.com)
- Radiologic investigation revealed new periosteal bone formation of the right and left ulnae and the left fibula, suggesting a recurrence of cortical hyperostosis. (medscape.com)
- [ 21 ] They concluded that the diagnosis of recurrent cortical hyperostosis should be considered for patients who experienced cortical hyperostosis in infancy and who present with similar symptoms during adolescence. (medscape.com)
- CAFFEY J. Infantile cortical hyperostoses. (medscape.com)
- Hyperphosphatemia -hyperostosis syndrome (HHS) is a rare autosomal recessive metabolic disorder characterized by elevated serum phosphate levels and radiological evidence of cortical hyperostosis. (wikidoc.org)
- Infantile cortical hyperostosis (Caffey disease) is characterized by spontaneous episodes of subperiosteal new bone formation along 1 or more bones commencing within the first 5 months of life. (jci.org)
- Individuals bearing the mutation, whether they had experienced an episode of cortical hyperostosis or not, had joint hyperlaxity, hyperextensible skin, and inguinal hernias resembling symptoms of a mild form of Ehlers-Danlos syndrome type III. (jci.org)
- Haplotype analyses of families with infantile cortical hyperostosis. (jci.org)
- Recurrent severe infantile cortical hyperostosis (Caffey disease) in siblings. (semanticscholar.org)
- Prenatal cortical hyperostosis with COL1A1 gene mutation. (semanticscholar.org)
- Radiological aspects of prenatal-onset cortical hyperostosis [Caffey Dysplasia]. (semanticscholar.org)
- Infantile cortical hyperostosis (ICH), also known as Caffey disease, was first reported by Roske in 1930 and described by Caffey and Silverman in 1945. (statpearls.com)
- Radiographic findings include cortical thickening (hyperostosis) and subperiosteal new bone formation. (statpearls.com)
- There is a prenatal form of the disease, called lethal prenatal cortical hyperostosis, that shows an autosomal recessive mode of inheritance and occurs before 35 weeks gestation. (statpearls.com)
- Various types of localised hyperostosis have been recognised including internal frontal hyperostosis, leontiasis ossea and infantile cortical hyperostosis Caffey's' disease. (fungionline.org.uk)
- Full TextCaffey: Disease or Infantile Cortical Hyperostosis: A Case Report. (fungionline.org.uk)
- Caffey disease or Infantile Cortical Hyperostosis ICH is a rare and mostly self limiting condition affecting young infants. (fungionline.org.uk)
- Infantile Cortical Hyperostosis An Inquiry into the Etiology and Pathogenesis NEJM. (fungionline.org.uk)
- THE syndrome that has become known as infantile cortical hyperostosis, after the suggestion of Caffey and Silverman, 1 is characterized by the usually sudden onset of swelling of the face, thorax or extremities, hyperirritability, fever, fluctuating course and roentgenographic evidence of periosteal new-bone formation. (fungionline.org.uk)
- generalized cortical hyperostosis a hereditary disorder beginning during puberty, marked by osteosclerosis of the skull, mandible, clavicles, ribs, and diaphyses of long bones, associated with elevated blood alkaline phosphatase. (fungionline.org.uk)
- Hyperphosphatemic hyperostosis syndrome (HHS) is characterized by hyperphosphatemia and episodes of diaphysitis and cortical hyperostosis visualized on x-rays. (biomedcentral.com)
- Radiologic findings of subperiosteal cortical hyperostosis of the diaphyses of the long bones (with sparing of the epiphyses), ribs, scapulae, clavicles, and mandible in a child age two months to five years suggest the diagnosis. (nih.gov)
- Radiologic findings of subperiosteal cortical hyperostosis of the diaphyses of the long bones (with sparing of the epiphyses), as well as the ribs, scapulae, clavicles, and mandible. (nih.gov)
- Clavicular cortical hyperostosis: new autoinflammatory entity or part of the juvenile spondyloarthropathies clinical picture? (biomedcentral.com)
- Clavicular cortical hyperostosis (CCH-variant of chronic recurrent multifocal osteomyelitis) is characterized by unilateral sterno-clavicular swelling. (biomedcentral.com)
Frontalis Interna9
- Hyperostosis frontalis interna: archaeological evidence of possible microevolution of human sex steroids? (uzh.ch)
- Hyperostosis frontalis interna is a restricted bilateral thickening of the frontal endocranial surface, which is frequently found in postmenopausal females today. (uzh.ch)
- This is again highlighted by the oldest known male European hyperostosis frontalis interna case in an adult Celtic from 100 BC presented here. (uzh.ch)
- Hyperostosis frontalis interna a find in women individual from Modern Times St. Martin Cathedral, Spisska Kapitula, Slovakia Antropoweb. (fungionline.org.uk)
- Hyperostosis frontalis interna HFI is an overgrowth of bony tissue on the inner plate of the frontal bone of the calvaria, the irregular thickening of the endocranium may be 1 cm or thicker. (fungionline.org.uk)
- Hyperostosis Frontalis Interna NORD National Organization for Rare Disorders. (fungionline.org.uk)
- Hyperostosis Frontalis Interna affects females 9 times more often than males. (fungionline.org.uk)
- Symptoms of the following disorders can be similar to those of Hyperostosis Frontalis Interna. (fungionline.org.uk)
- frontal internal hyperostosis hyperostosis frontalis interna a new formation of bone tissue protruding in patches on the internal surface of the cranial bones in the frontal region, most commonly affecting women near menopause. (fungionline.org.uk)
Pustulosis3
- The concept of SAPHO syndrome (synovitis, acne, pustulosis, hyperostosis, osteitis) includes 4 subgroups of osteoarticular disorders: (1) rheumatologic manifestations associated with acne conglobata or acne fulminans or inversa hidradenitis suppurativa, (2) pustulosis palmoplantaris, (3) sternocostoclavicular hyperostosis, and (4) chronic multifocal recurrent osteomyelitis. (medscape.com)
- The two most common entities among generally rare but under-diagnosed autoinflammatory bone disorders are chronic recurrent multifocal osteomyelitis (CRMO) and synovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome. (unboundmedicine.com)
- Synovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome is an inflammatory clinical condition with aseptic bone lesions and characteristic skin manifestations. (koreamed.org)
Osteitis1
- However, aseptic osteitis with hyperostosis, particularly of the thoracic joints, is a hallmark of SAPHO syndrome, and it may represent a feature that distinguishes SAPHO syndrome from the arthropathy of hidradenitis suppurativa and acne conglobata. (medscape.com)
Spine2
- Hyperostosis of the spine in an adult population. (bmj.com)
- A cervical spine CT highlighted the hyperostosis with a consequent anterior displacement of oropharynx. (minervamedica.it)
Corticalis3
- LRP5 related high bone density phenotypes - Hyperostosis corticalis generalisata, benign form of worth, with torus palatinus or endosteal hyperostosis (MIM 144750) is an autosomal dominant disorder caused by mutations in the LDL receptor-related protein 5 (LRP5) gene. (ctgt.net)
- The clinical findings in VBCH2 are similar to those in hyperostosis corticalis generalisata. (ctgt.net)
- The detection of a shared LRP5 mutation in patients with VBCH2 and hyperostosis corticalis generalisata indicates that this is indeed the case. (ctgt.net)
Bone2
- Hyperostosis is an excessive growth of bone. (wikipedia.org)
- Porotic hyperostosis, also known as osteoporosis symmetrica, cribra crani, hyperostosis spongiosa, and symmetrical osteoporosis is a pathological condition that affects bones of the cranial vault, and is characterized by localized areas of spongy or porous bone tissue. (wikipedia.org)
Forestier's1
- Forestier's' disease was first described by Jacques Forestier and his student Jaume Rotes-Querol in 1950 under the name senile ankylosing vertebral hyperostosis. (fungionline.org.uk)
Disease5
- Sternocostoclavicular hyperostosis (SCCH) is an ill-recognized, rarely diagnosed disease. (mdpi.com)
- The disease causes progressive hyperostosis, fusion of the sternocostoclavicular joints, and soft tissue ossification. (mdpi.com)
- Information on all these conditions is provided by Ortner 2003, but apart from internal frontal hyperostosis and Caffey's' disease e.g. (fungionline.org.uk)
- The most common site of the disease is the upper anterior chest wall, characterized by predominantly osteosclerotic lesions, hyperostosis, and arthritis of the adjacent joints. (ctdbase.org)
- The degree of hyperostosis varies among individuals with Camurati-Engelmann disease as does the age at which they experience their first symptoms. (medlineplus.gov)
Porotic hyperostosis8
- This condition was widely accepted as a result of anemia, which is typically due to an iron deficient diet, but several lines of evidence suggest that the accelerated loss and compensatory over-production of red blood cells seen in hemolytic and megaloblastic anemia are the most likely proximate causes of porotic hyperostosis. (wikipedia.org)
- A sub-discipline known as paleonutrition has focused on the presence of porotic hyperostosis, among other nutritional disorders. (wikipedia.org)
- From this perspective, porotic hyperostosis could be viewed as a biological attempt to adapt to the environment, rather than an indicator of malnutrition. (wikipedia.org)
- 1968. Porotic hyperostosis and the Gelligaer skull. (wikipedia.org)
- Stuart-Macadam P. 1992 Porotic hyperostosis: a new perspective. (wikipedia.org)
- Walker PL et al (2009) The causes of porotic hyperostosis and cribra orbitalia: a reappraisal of the iron-deficiency-anemia hypothesis. (wikipedia.org)
- Several lines of evidence suggest that the accelerated loss and compensatory over-production of red blood cells seen in hemolytic and megaloblastic anemias is the most likely proximate cause of porotic hyperostosis. (nih.gov)
- Although cranial vault and orbital roof porosities are sometimes conflated under the term porotic hyperostosis, paleopathological and clinical evidence suggests they often have different etiologies. (nih.gov)
Vertebral hyperostosis1
- Ankylosing vertebral hyperostosis and pulmonary function. (fungionline.org.uk)
Endosteal hyperostosis6
- Endosteal hyperostosis has various causes and these are reviewed by Whyte 1998, but these are rare conditions. (fungionline.org.uk)
- Endosteal hyperostosis was encountered in a 26-year-old-man and his 6-month-old daughter. (biomedcentral.com)
- To the best of our knowledge, this is the first clinical report describing distinctive spinal changes in association with fractures and endosteal hyperostosis. (biomedcentral.com)
- More than 13 kindreds with endosteal hyperostosis have been reported. (biomedcentral.com)
- We present a father and daughter with endosteal hyperostosis. (biomedcentral.com)
- We found no previous reports describing this constellation of spinal abnormalities in association with autosomal dominant, endosteal hyperostosis. (biomedcentral.com)
Calvarial hyperostosis2
- Calvarial hyperostosis presenting as unilateral exophthalmos in a female English Springer Spaniel. (semanticscholar.org)
- PubMed is a searchable database of medical literature and lists journal articles that discuss Calvarial hyperostosis. (cdc.gov)
Sternocostoclavicular1
- Treatment-Refractory Sternocostoclavicular Hyperostosis. (nih.gov)
Definition1
- Hyperostosis Definition of Hyperostosis at Dictionary.com. (fungionline.org.uk)
Skeletal hyperostosis16
- Diffuse idiopathic skeletal hyperostosis (DISH) describes a phenomenon characterized by a tendency toward ossification of ligaments. (omicsonline.org)
- Olivieri I, Diffuse Idiopathic skeletal hyperostosis may give the typical postural abnormalities of advanced ankylosing spondylitis. (edu.pl)
- Shaul, Stephen R. Diffuse idiopathic skeletal hyperostosis (DISH) [ankylosing hyperostosis of forestier and Rotes-Querol]. (edu.pl)
- Diffuse idiopathic skeletal hyperostosis and its relation to back pain among older men: the MrOS Study. (edu.pl)
- Comprehensive radiographic evaluation of diffuse idiopathic skeletal hyperostosis: development and interrater reliability of a scoring system. (edu.pl)
- Mader R, Current therapeutic options in the management of diffuse idiopathic skeletal hyperostosis. (edu.pl)
- The surgical management of dysphagia secondary to diffuse idiopathic skeletal hyperostosis. (edu.pl)
- 2013). Late onset vertebral fusions may be associated with bone hyperostosis and include spondylosis deformans, diffuse idiopathic skeletal hyperostosis (DISH) and spondyloarthropathies such as osteoarthritis of the facet joints and ankylosing spondylitis (Reswick, 1985). (palaeo-electronica.org)
- For example, the term spondylosis deformans has occasionally been used to describe the condition more properly called diffuse idiopathic skeletal hyperostosis or DISH (Kranenburg et al. (palaeo-electronica.org)
- 2009). The coexistence of ankylosing spondylitis and diffuse idiopathic skeletal hyperostosis - A postmortem diagnosis . (up.pt)
- While head restraints are higher and more forward providing support for the head and neck, serious-to-fatal injuries to the thoracic and cervical spine have been seen in occupants with spinal disorders, such as DISH (diffuse idiopathic skeletal hyperostosis), ankylosis, spondylosis and/or osteophytes that ossify the joints in the spine. (sae.org)
- It seems that for a very long time my spinal column had been abnormally narrowing from a kind of degenerative arthritis known as Forestier's disease, or DISH (diffuse idiopathic skeletal hyperostosis). (washingtonmonthly.com)
- UPDATE I HAVE FOUND A FACEBOOK GROUP OF D.I.S.H SUFFERER'S D.I.S.H Facebook Group Also known as Forestier's disease, Diffuse Idiopathic Skeletal Hyperostosis causes stiffness in your upper back and may also affect your neck and lower back. (robhealey.com.au)
- When bleeding control is diffuse idiopathic skeletal hyperostosis (dish) is char- siderin) often develops. (aestheticscienceinstitute.edu)
- [Aggie RN] I have a very severe diffuse idiopathic skeletal hyperostosis. (huangsmassagelab.com)
- Diffuse idiopathic skeletal hyperostosis as reflected in the paleontologic record: dinosaurs and early mammals. (semanticscholar.org)
Diffuse1
- Diffuse Paget's disease of bone metastatic disease, especially prostate carcinoma chronic, severe anaemia hyperparathyroidism acromegaly osteopetrosis hyperostosis interja interna long-term phenytoin use genetic diseases rare Camurati-Engelmann disease frontometaphyseal dysplasia craniodiaphysial dysplasia Focal meningioma fibrous dysplasia Paget's disease of bone metastatic disease, especially prostate carcinoma esthesioneuroblastoma: The condition is generally of no clinical significance and an incidental finding. (protzonbeer.com)
Frontalis interna5
- Hyperostosis Frontalis Interna is characterized by the thickening of the frontal bone of the skull. (protzonbeer.com)
- Hyperostosis frontalis interna is characterised by benign overgrowth of the inner table of the frontal bone. (protzonbeer.com)
- Hyperostosis Frontalis Interna affects females 9 times more often than males. (protzonbeer.com)
- In she were performed imaging of the skull where was observed the presence of extensive hyperostosis frontalis interna, cortical atrophy and a left thalamic lacunar infarction. (protzonbeer.com)
- Hyperostosis Frontalis Interna internq been found in multiple generations suggesting that the disorder may be inherited as a dominant trait. (protzonbeer.com)
Meningioma1
- Other conditions that may be found in patients with this disorder are: Hyperostosis associated with meningioma of the cranial base: Vision disturbances and deafness may develop in some cases. (protzonbeer.com)
Acne1
- Mandibular hyperostosis in a patient receiving orthodontic treatment while on isotretinoin for acne. (ortodontiamarcelofraga.com.br)
Characterized by benign1
- Osteitis condensans ilii, also known as osteopathia condensans ilii or hyperostosis triangularis ilii in Germany, is characterized by benign sclerosis of the ilium adjacent to the sacroiliac (SI) joint , typically bilateral and triangular in shape. (radiopaedia.org)
Arthritis1
- Some other potential but infrequent causes include infections in joints in the rib cage (septic arthritis), polychondritis, and sternoclavicular hyperostosis. (jbmc.com.br)
Skull3
- Differential Diagnosis The differential is that of hyperostosis of the skull and includes: Investigational Therapies Information on current clinical trials is posted on the Internet at www. (protzonbeer.com)
- A skull X-ray revealed calvarial hyperostosis and a normal sellar outline. (bioscientifica.com)
- Craniodiaphyseal dysplasia is a severe bone dysplasia characterized by massive generalized hyperostosis and sclerosis, especially involving the skull and facial bones. (mendelian.co)
Treatment1
- The principle of comprehensive treatment applies to the treatment of hyperostosis. (edu.pl)
Hair1
- It is marked by generalized pruritus, desquamation of the skin, loss of hair, and hyperostoses. (thefreedictionary.com)
Results1
- ConclusionsOur results suggest that hyperostosis of the posterior longitudinal ligament in OPLL may not be associated with bone strength and bone mineral status at the extremities. (medworm.com)
