Tumors or cancer in the JEJUNUM region of the small intestine (INTESTINE, SMALL).
Tumors or cancer of the PANCREAS. Depending on the types of ISLET CELLS present in the tumors, various hormones can be secreted: GLUCAGON from PANCREATIC ALPHA CELLS; INSULIN from PANCREATIC BETA CELLS; and SOMATOSTATIN from the SOMATOSTATIN-SECRETING CELLS. Most are malignant except the insulin-producing tumors (INSULINOMA).
New abnormal growth of tissue. Malignant neoplasms show a greater degree of anaplasia and have the properties of invasion and metastasis, compared to benign neoplasms.
Neoplasms containing cyst-like formations or producing mucin or serum.
Tumors or cancer of the SKIN.
Two or more abnormal growths of tissue occurring simultaneously and presumed to be of separate origin. The neoplasms may be histologically the same or different, and may be found in the same or different sites.

Descriptive epidemiology of small intestinal malignancies: the German Cancer Registry experience. (1/126)

In the first population-based analysis of certain epidemiologic features of primary malignancies of the small intestine in Germany, we used data from the Saarland Cancer Registry (1982-1993) and from the former National Cancer Registry of the German Democratic Republic (1976-1989). The age-standardized incidence rates for ages 0-74 years is 3.3-6.2 per million per year. The average incidence rates of the federal state Saarland are for men about 1.3 times and for women about 1.4 times the rate of the former German Democratic Republic. After the age of 30 years, the incidence rates increased with increasing age. Incidence rates for carcinoids levelled off after the age of 54 years. Rates for men were 35-40% higher than for women after adjusting for age. The risk for carcinomas, malignant carcinoids and malignant lymphoma were higher for men than for women.  (+info)

Emergency abdominal surgery for small bowel perforation secondary to metastatic lung cancer. (2/126)

Emergency surgery for bowel perforation caused by metastases from lung cancer is rare. Two cases of small bowel perforation due to metastasizing lung cancer are reported. Both patients were admitted as a surgical emergency case. One of the two patients presented herein survived and was discharged from the hospital. Perforated small bowel due to metastatic lung cancer is a highly fatal event that occurs in the late phases of the disease. Despite the poor prognosis, early and appropriate therapy will occasionally yield successful surgical palliation. Patients with known lung cancer who develop abdominal complaints should be examined thoroughly and treated quickly.  (+info)

Presence of sorbin in human digestive tract and endocrine digestive tumours. (3/126)

BACKGROUND: Sorbin, a 153 amino acid peptide isolated from porcine intestine, was localised by immunohistochemistry in endocrine cells of the intestinal mucosa and pancreas and in the enteric nervous system in the pig. AIMS: To identify sorbin cells in normal human digestive tissues and to explore the expression of sorbin in 37 digestive endocrine tumours: 14 intestinal carcinoid tumours and 23 endocrine pancreatic tumours including six insulinomas. METHODS: Two polyclonal antibodies against the C-terminal and the N-terminal sequences of porcine sorbin raised in rabbit were used to evaluate sorbin expression by immunohistochemistry. RESULTS: In the human digestive tract, sorbin, characterised by both C-terminal and N-terminal immunoreactivity, was found in enterochromaffin cells of the gastric and intestinal epithelium from the pyloric junction to the descending colon. C-Terminal sorbin immunoreactivity alone was found in plexii from the enteric nervous system and in some insulin-containing cells of normal pancreas. C-Terminal and N-terminal antibodies disclosed sorbin in five of 14 intestinal carcinoid tumours; C-terminal antibody alone disclosed a C-terminal sorbin peptide in two of six insulinomas and three of 17 endocrine pancreatic tumours. The presence of sorbin was not associated with a specific clinical syndrome. CONCLUSIONS: Sorbin is present in the digestive tract in several forms. It is expressed in some intestinal and pancreatic endocrine tumours.  (+info)

Gastrointestinal stromal tumors of the small intestine that expressed c-kit protein. (4/126)

We report two patients with gastrointestinal stromal tumors (GISTs) of the small intestine that expressed c-kit protein (CD117). One was a 68-year-old woman with epigastralgia and vomiting. A submucosal tumor of the upper jejunum was detected, and partial resection was carried out. The histology revealed a GIST negative for CD34 but positive for CD117. The other was a 42-year-old woman with progressive anemia, melena and lower abdominal pain. Intussusception was detected, and a partial resection was carried out. A submucosal tumor of the lower jejunum was noted. The histology revealed a GIST positive for both CD34 and CD117.  (+info)

Malignancy risk prediction for primary jejunum-ileal tumors. (5/126)

This work is aimed at identifying factors associated with primary jejunum-ileal tumors malignancy, defining a prediction model with sensitivity, specificity and accuracy to distinguish malign from benign neoplasms. These tumors are rare, have highly unspecific presentation and, frequently, are diagnosed late. We reviewed the charts of 42 patients with primary jejunum-ileal tumors treated in the Department of General Surgery of Rio de Janeiro State University Hospital, Rio de Janeiro, RJ, Brazil, from 1969 to 1998. We performed bivariate analyses, based on chi 2 test, searching associations between tumors malignancy and demographic and clinical variables. Then logistic regression was employed to consider the independent effect of variables previously identified on malignancy risk. The malign tumors included 11 adenocarcinomas, 7 leiomyosarcomas, 5 carcinoids and 4 lymphomas; the benign tumors included 10 leiomyomas, 2 hamartomas, and single cases of adenoma, multiple neurilemoma and choristoma. The bivariate analyses indicated the association between malignancy and palpable abdominal mass (P = 0.003), period from signs and symptoms onset to diagnosis (P = 0.016), anemia (P = 0.020), anorexia (P = 0.003), abdominal pain (P = 0.031), weight loss (P = 0.001), nausea and vomit (P = 0.094), and intestinal obstruction (P = 0.066); no association with patients demographic characteristics were found. In the final logistic regression model, weight loss, anemia and intestinal obstruction were statistically associated with the dependent variable of interest. Based only on three variables--weight loss, anemia and intestinal obstruction--the model defined was able to predict primary jejunum-ileal tumors malignancy with sensitivity of 85.2%, specificity of 80.0%, and accuracy of 83.3%.  (+info)

An insight into the genetic pathway of adenocarcinoma of the small intestine. (6/126)

BACKGROUND: Although the adenoma to carcinoma pathway in colorectal cancer is well described, the mechanisms of carcinogenesis in the small intestine remain unclear. AIMS: The aim of this study was to investigate candidate genes in the genetic pathway of adenocarcinoma of the small intestine. SUBJECTS AND METHODS: A total of 21 non-familial, non-ampullary adenocarcinomas of the small intestine were analysed. DNA was extracted from formalin fixed paraffin wax embedded tissue using standard techniques. The replication error (RER) status was determined by amplification of BAT26. The mutation cluster region (MCR) of the adenomatous polyposis coli (APC) gene was screened using polymerase chain reaction single strand conformational polymorphism and direct sequencing. Immunohistochemistry was performed on formalin fixed paraffin wax embedded tissue using monoclonal antibodies for hMLH1, hMSH2, beta-catenin, E-cadherin, and p53. RESULTS: Fourteen male and seven female patients with a median age of 64 years (range 21-85) presented with adenocarcinoma of the duodenum (10), jejunum (7), and ileum (4). One cancer (5%) was found to be RER+, and all tumours stained positive for hMLH1 and hMSH2. No mutations were detected in the MCR of the APC gene. beta-Catenin showed increased nuclear expression with loss of membranous staining in 10 cancers (48%). Absent or decreased membrane expression of E-cadherin was found in eight cancers (38%). Strong staining of p53 was found in the nucleus of five cancers (24%). CONCLUSION: We did not detect mutations in the MCR of the APC gene, and this suggests that adenocarcinoma of the small intestine may follow a different genetic pathway to colorectal cancer. Abnormal expression of E-cadherin and beta-catenin was common and reflects an early alternative to APC in this pathway in which mutations may be found in adenocarcinoma of the small intestine.  (+info)

Ataxia in the setting of complicated enteropathy: double jeopardy. (7/126)

The differential diagnosis of subacute onset ataxia in the setting of enteropathy is wide. A 54 year old patient with a pancerebellar syndrome and known ulcerative jejunoileitis is described. Small bowel biopsy showed evidence of enteropathy associated T cell lymphoma and subsequent neuropathological analysis and immunophenotyping confirmed metastasis of this tumour to the cerebellum. The presence of anti-gliadin antibodies and MRI evidence of a more longstanding process suggested additional immunologically mediated cerebellar dysfunction. Lymphomatous involvement of the CNS is rare in patients with complicated enteropathies, and has not been previously reported to involve the cerebellar parenchyma. This diagnostic possibility should be borne in mind before attributing cerebellar dysfunction in patients with the coeliac related enteropathies to nutritional compromise or immunological dysfunction (gluten ataxia) alone.  (+info)

Primary jejunoileal neoplasmas: a review of 60 cases. (8/126)

AIM: Primary neoplasmas of the jejunum and ileum are infrequent and lack specific manifestations and inaccessibility of conventional endoscopy, so the diagnosis of these tumors are usually delayed. So far the data of primary jejunoileal neoplasmas is still scarce, especially in Chinese medical literature in English. There may be some differences among the Chinese and the westerners in jejunoileal neoplasmas. METHODS: A retrospective analysis was made on clinical findings and pathological types. RESULTS: Of the 60 patients with jejunal or ileal neoplasmas, the most frequent symptom was abdominal pain (57 %), followed by tarry stool (43 %) and hematochezia (10 %). Abdominal mass (40 %) was the most common finding on physical examination, followed by anemia and weight loss (35 %). 67 % of the jejunoileal neoplasms were located in the jejunum. Among the malignant neoplasmas (68 %), malignant stroma (47 %) was most common, while the benign stromoma (20 %) was the most common benign neoplasmas. Preoperatively, 40 patients (67 %) were diagnosed as small bowel neoplasmas, of which 34 were found by enteroclysis. Abdominal mass was shown by CT in 18 cases and by ultrasonography in 13. The mean duration of symptoms before diagnosis was 7 months. In 41 patients with malignant tumors, the duration of symptoms before diagnosis exceeded 12 months in 21 cases, lymphatic or distant metastases were found in 26 (63 %)cases during operation. An emergency laparotomy was performed in 4 patients (7 %) owing to intestinal obstruction or perforation. CONCLUSION: Primary jejunoileal neoplasmas in Chinese present some difference from Westerners on clinical features and histopathologic types. Enteroclysis remains the major relevant diagnostic procedure in this study, the misdiagnotic rate is high preoperatively due to failure of detection by conventional imaging procedures such as CT and inaccessibility of routine endoscopy. For the suspected patients, combined application of aforementioned procedures may facilitate early diagnosis. The wireless capsule endoscopy may improve the diagnostic rate of jejunoileal neoplasmas in the future.  (+info)

Jejunal neoplasms refer to abnormal growths or tumors in the jejunum, which is the middle section of the small intestine. These neoplasms can be benign (non-cancerous) or malignant (cancerous). Malignant jejunal neoplasms are often aggressive and can spread to other parts of the body, making them potentially life-threatening.

There are several types of jejunal neoplasms, including:

1. Adenocarcinomas: These are cancerous tumors that develop from the glandular cells lining the jejunum. They are the most common type of jejunal neoplasm.
2. Carcinoid tumors: These are slow-growing neuroendocrine tumors that arise from the hormone-producing cells in the jejunum. While they are usually benign, some can become malignant and spread to other parts of the body.
3. Gastrointestinal stromal tumors (GISTs): These are rare tumors that develop from the connective tissue cells in the jejunum. They can be benign or malignant.
4. Lymphomas: These are cancerous tumors that develop from the immune system cells in the jejunum. They are less common than adenocarcinomas but can be aggressive and spread to other parts of the body.
5. Sarcomas: These are rare cancerous tumors that develop from the connective tissue cells in the jejunum. They can be aggressive and spread to other parts of the body.

Symptoms of jejunal neoplasms may include abdominal pain, bloating, diarrhea, weight loss, and bleeding in the stool. Treatment options depend on the type and stage of the neoplasm but may include surgery, chemotherapy, radiation therapy, or a combination of these approaches.

Pancreatic neoplasms refer to abnormal growths in the pancreas that can be benign or malignant. The pancreas is a gland located behind the stomach that produces hormones and digestive enzymes. Pancreatic neoplasms can interfere with the normal functioning of the pancreas, leading to various health complications.

Benign pancreatic neoplasms are non-cancerous growths that do not spread to other parts of the body. They are usually removed through surgery to prevent any potential complications, such as blocking the bile duct or causing pain.

Malignant pancreatic neoplasms, also known as pancreatic cancer, are cancerous growths that can invade and destroy surrounding tissues and organs. They can also spread (metastasize) to other parts of the body, such as the liver, lungs, or bones. Pancreatic cancer is often aggressive and difficult to treat, with a poor prognosis.

There are several types of pancreatic neoplasms, including adenocarcinomas, neuroendocrine tumors, solid pseudopapillary neoplasms, and cystic neoplasms. The specific type of neoplasm is determined through various diagnostic tests, such as imaging studies, biopsies, and blood tests. Treatment options depend on the type, stage, and location of the neoplasm, as well as the patient's overall health and preferences.

Neoplasms are abnormal growths of cells or tissues in the body that serve no physiological function. They can be benign (non-cancerous) or malignant (cancerous). Benign neoplasms are typically slow growing and do not spread to other parts of the body, while malignant neoplasms are aggressive, invasive, and can metastasize to distant sites.

Neoplasms occur when there is a dysregulation in the normal process of cell division and differentiation, leading to uncontrolled growth and accumulation of cells. This can result from genetic mutations or other factors such as viral infections, environmental exposures, or hormonal imbalances.

Neoplasms can develop in any organ or tissue of the body and can cause various symptoms depending on their size, location, and type. Treatment options for neoplasms include surgery, radiation therapy, chemotherapy, immunotherapy, and targeted therapy, among others.

Neoplasms: Neoplasms refer to abnormal growths of tissue that can be benign (non-cancerous) or malignant (cancerous). They occur when the normal control mechanisms that regulate cell growth and division are disrupted, leading to uncontrolled cell proliferation.

Cystic Neoplasms: Cystic neoplasms are tumors that contain fluid-filled sacs or cysts. These tumors can be benign or malignant and can occur in various organs of the body, including the pancreas, ovary, and liver.

Mucinous Neoplasms: Mucinous neoplasms are a type of cystic neoplasm that is characterized by the production of mucin, a gel-like substance produced by certain types of cells. These tumors can occur in various organs, including the ovary, pancreas, and colon. Mucinous neoplasms can be benign or malignant, and malignant forms are often aggressive and have a poor prognosis.

Serous Neoplasms: Serous neoplasms are another type of cystic neoplasm that is characterized by the production of serous fluid, which is a thin, watery fluid. These tumors commonly occur in the ovary and can be benign or malignant. Malignant serous neoplasms are often aggressive and have a poor prognosis.

In summary, neoplasms refer to abnormal tissue growths that can be benign or malignant. Cystic neoplasms contain fluid-filled sacs and can occur in various organs of the body. Mucinous neoplasms produce a gel-like substance called mucin and can also occur in various organs, while serous neoplasms produce thin, watery fluid and commonly occur in the ovary. Both mucinous and serous neoplasms can be benign or malignant, with malignant forms often being aggressive and having a poor prognosis.

Skin neoplasms refer to abnormal growths or tumors in the skin that can be benign (non-cancerous) or malignant (cancerous). They result from uncontrolled multiplication of skin cells, which can form various types of lesions. These growths may appear as lumps, bumps, sores, patches, or discolored areas on the skin.

Benign skin neoplasms include conditions such as moles, warts, and seborrheic keratoses, while malignant skin neoplasms are primarily classified into melanoma, squamous cell carcinoma, and basal cell carcinoma. These three types of cancerous skin growths are collectively known as non-melanoma skin cancers (NMSCs). Melanoma is the most aggressive and dangerous form of skin cancer, while NMSCs tend to be less invasive but more common.

It's essential to monitor any changes in existing skin lesions or the appearance of new growths and consult a healthcare professional for proper evaluation and treatment if needed.

Multiple primary neoplasms refer to the occurrence of more than one primary malignant tumor in an individual, where each tumor is unrelated to the other and originates from separate cells or organs. This differs from metastatic cancer, where a single malignancy spreads to multiple sites in the body. Multiple primary neoplasms can be synchronous (occurring at the same time) or metachronous (occurring at different times). The risk of developing multiple primary neoplasms increases with age and is associated with certain genetic predispositions, environmental factors, and lifestyle choices such as smoking and alcohol consumption.

... jejunal neoplasms MeSH C06.301.371.767 - stomach neoplasms MeSH C06.301.371.883 - zollinger-ellison syndrome MeSH C06.301. ... jejunal neoplasms MeSH C06.405.249.767 - stomach neoplasms MeSH C06.405.249.883 - zollinger-ellison syndrome MeSH C06.405. ... jejunal diseases MeSH C06.405.469.600.523 - jejunal neoplasms MeSH C06.405.469.637 - malabsorption syndromes MeSH C06.405. ... common bile duct neoplasms MeSH C06.130.320.120 - bile duct neoplasms MeSH C06.130.320.120.280 - common bile duct neoplasms ...
... duodenal neoplasms MeSH C04.588.274.476.411.501 - ileal neoplasms MeSH C04.588.274.476.411.523 - jejunal neoplasms MeSH C04.588 ... skull base neoplasms MeSH C04.588.149.828 - spinal neoplasms MeSH C04.588.180.260 - breast neoplasms, male MeSH C04.588.180.390 ... bile duct neoplasms MeSH C04.588.274.120.250.250 - common bile duct neoplasms MeSH C04.588.274.120.401 - gallbladder neoplasms ... femoral neoplasms MeSH C04.588.149.721 - skull neoplasms MeSH C04.588.149.721.450 - jaw neoplasms MeSH C04.588.149.721.450.583 ...
Along with neoplasms of the sebaceous gland, this patient developed cerebral neoplasms, characteristic of Turcot syndrome. ... 1999). "Muir-Torre syndrome: a case report of a patient with concurrent jejunal and ureteral cancer and a review of the ... Age of onset of first sebaceous neoplasm: 2 = 2 points. Personal history of Lynch related cancers: No = 0 points, Yes = 1 point ... 2014). "A clinical scoring system to identify patients with sebaceous neoplasms at risk for the Muir-Torre variant of Lynch ...
Jejunal, duodenal mucosa or Brunner's tissue were each found in 2% of ectopic cases. Heterotopic rests of gastric mucosa and ... Abscess formation in the abdominal wall Fibrous cord increases the risk of volvulus formation and internal herniation Neoplasms ...
PEG tubes may also be extended into the small intestine by passing a jejunal extension tube (PEG-J tube) through the PEG tube ... difficulties in locating stomach position by digital indentation of stomach and transillumination Gastric wall neoplasm ... Gail Waldby, "PEG-J Gastrostomy drainage jejunal feeding tubes" "Untitled Document". Archived from the original on 2011-07-16. ...
Matutes E (May 2018). "The 2017 WHO update on mature T- and natural killer (NK) cell neoplasms". International Journal of ... Zullo A, De Francesco V, Manta R, Ridola L, Lorenzetti R (December 2017). "A Challenging Diagnosis of Jejunal Adenocarcinoma in ...
Carrington syndrome Cartilage hair hypoplasia like syndrome Cartilage-hair hypoplasia Cartilaginous neoplasms Cartwright-Nelson ... Corneal endothelium dystrophy Cornelia de Lange syndrome Corneodermatoosseous syndrome Coronal synostosis syndactyly jejunal ... hypoxia Cerebral malformations hypertrichosis claw hands Cerebral palsy Cerebral thrombosis Cerebral ventricle neoplasms ... Choriocarcinoma Chorioretinitis Chorioretinopathy dominant form microcephaly Choroid plexus cyst Choroid plexus neoplasms ...
"Jejunal Neoplasms" by people in UAMS Profiles by year, and whether "Jejunal Neoplasms" was a major or minor topic of these ... "Jejunal Neoplasms" is a descriptor in the National Library of Medicines controlled vocabulary thesaurus, MeSH (Medical Subject ... Below are the most recent publications written about "Jejunal Neoplasms" by people in Profiles over the past ten years. ... Below are MeSH descriptors whose meaning is more general than "Jejunal Neoplasms". ...
... jejunal neoplasms MeSH C06.301.371.767 - stomach neoplasms MeSH C06.301.371.883 - zollinger-ellison syndrome MeSH C06.301. ... jejunal neoplasms MeSH C06.405.249.767 - stomach neoplasms MeSH C06.405.249.883 - zollinger-ellison syndrome MeSH C06.405. ... jejunal diseases MeSH C06.405.469.600.523 - jejunal neoplasms MeSH C06.405.469.637 - malabsorption syndromes MeSH C06.405. ... common bile duct neoplasms MeSH C06.130.320.120 - bile duct neoplasms MeSH C06.130.320.120.280 - common bile duct neoplasms ...
... cecal neoplasms/ or exp *duodenal neoplasms/ or exp *ileal neoplasms/ or exp *jejunal neoplasms/ or exp *stomach neoplasms/ or ... cecal neoplasms/ or exp *duodenal neoplasms/ or exp *ileal neoplasms/ or exp *jejunal neoplasms/ or exp *stomach neoplasms/ or ... pc or exp COLONIC NEOPLASMS/pc or exp SIGMOID NEOPLASMS/pc or exp RECTAL NEOPLASMS/pc or exp ANUS NEOPLASMS/pc or exp NEOPLASMS ... exp CERVIX NEOPLASMS/pc or exp UTERINE NEOPLASMS/pc or exp VAGINAL NEOPLASMS/pc or exp GENITAL NEOPLASMS, FEMALE/pc or exp ...
Jejunal Neoplasms * Leiomyosarcoma * Male * Prognosis Identity. Digital Object Identifier (DOI) * 10.1016/s0022-3468(97)90689-8 ... Visceral metastases from these neoplasms are atypical, and recorded long-term prognosis may be favorable, unlike their ...
... low grade neuroendocrine neoplasm (carcinoid tumor) that arises from the jejunum. The mitotic count is less than 2 per 10 HPF ... Intestinal neoplasm*Jejunal neoplasm*Jejunal neuroendocrine tumor, well differentiated, low or intermediate grade*Jejunal ... jejunal carcinoid tumor; jejunal carcinoid tumour; Jejunal NET G1; jejunal NET G1; Jejunal Neuroendocrine Tumor G1; jejunal ... grade 1 neuroendocrine neoplasm of jejunum; Jejunal Carcinoid Tumor; ...
O Jaw neoplasm,O Jaw pain,O Jaw swelling,O Jejunal adenocarcinoma,O Jejunal arteriovenous malformation,O Jejunal atresia,O ... O Neoplasm of the inner ear,O Neoplasm of the large intestine,O Neoplasm of the larynx,O Neoplasm of the lip,O Neoplasm of the ... O Neoplasm of the middle ear,O Neoplasm of the nail,O Neoplasm of the nervous system,O Neoplasm of the nose,O Neoplasm of the ... O Neoplasm of the colon,O Neoplasm of the ear,O Neoplasm of the endocrine system,O Neoplasm of the eye,O Neoplasm of the ...
Tripe palms in the absence of AN is more often associated with lung neoplasms, especially non-small cell carcinomas of the ... although it may rarely occur in the presence of jejunal and rectal adenocarcinomas, villous atrophy of the small intestine, ... Sellheyer K, Krahl D. Ber-EP4 enhances the differential diagnostic accuracy of cytokeratin 7 in pagetoid cutaneous neoplasms. J ... A family history of endocrine neoplasms may be uncovered in cases of glucagonoma associated with multiple endocrine neoplasia. ...
Of the 32 patients with neoplasms, there were 13 adenocarcinomas: six primary ileal, four duodenal and three jejunal. Safety, ...
Proximal jejunal gastrointestinal stromal tumor that is completely exophytic and not visible at small-bowel barium examination ... CT evaluation of small bowel neoplasms: spectrum of disease. Radiographics. 1998 Mar-Apr. 18(2):379-92. [QxMD MEDLINE Link]. ... Proximal jejunal gastrointestinal stromal tumor that is completely exophytic and not visible at small-bowel barium examination ... Proximal jejunal gastrointestinal stromal tumor that is completely exophytic and not visible at small-bowel barium examination ...
Conclusions: Free jejunal grafts in larynx-preserving surgery can be performed safely and reliably in patients with low ... Conclusions: Free jejunal grafts in larynx-preserving surgery can be performed safely and reliably in patients with low ... Conclusions: Free jejunal grafts in larynx-preserving surgery can be performed safely and reliably in patients with low ... Conclusions: Free jejunal grafts in larynx-preserving surgery can be performed safely and reliably in patients with low ...
Jejunal Neoplasms Jejunoileal Bypass Jejunostomy Jejunum Jelling Agents use Gelling Agents Jellyfish Venoms use Cnidarian ...
Jejunal Neoplasms Jejunoileal Bypass Jejunostomy Jejunum Jelling Agents use Gelling Agents Jellyfish Venoms use Cnidarian ...
Jejunal Neoplasms Jejunoileal Bypass Jejunostomy Jejunum Jelling Agents use Gelling Agents Jellyfish Venoms use Cnidarian ...
Jejunal Neoplasms. Jejunoileal Bypass. Jejunostomy. Jejunum. Jelling Agents use Gelling Agents. Jellyfish Venoms use Cnidarian ...
Jejunal Neoplasms Jejunoileal Bypass Jejunostomy Jejunum Jelling Agents use Gelling Agents Jellyfish Venoms use Cnidarian ...
Jejunal Neoplasms Jejunoileal Bypass Jejunostomy Jejunum Jelling Agents use Gelling Agents Jellyfish Venoms use Cnidarian ...
Jejunal Neoplasms Jejunoileal Bypass Jejunostomy Jejunum Jelling Agents use Gelling Agents Jellyfish Venoms use Cnidarian ...
Jejunal Neoplasms Jejunoileal Bypass Jejunostomy Jejunum Jelling Agents use Gelling Agents Jellyfish Venoms use Cnidarian ...
Jejunal Neoplasms Jejunoileal Bypass Jejunostomy Jejunum Jelling Agents use Gelling Agents Jellyfish Venoms use Cnidarian ...
Jejunal Neoplasms Jejunoileal Bypass Jejunostomy Jejunum Jelling Agents use Gelling Agents Jellyfish Venoms use Cnidarian ...
Jejunal Neoplasms Jejunoileal Bypass Jejunostomy Jejunum Jelling Agents use Gelling Agents Jellyfish Venoms use Cnidarian ...
Jejunal Neoplasms Jejunoileal Bypass Jejunostomy Jejunum Jelling Agents use Gelling Agents Jellyfish Venoms use Cnidarian ...
Case report: Life-threatening haematochezia from a jejunal leiomyoma. Chih Yen Chen, Ching Liang Lu, Su Shun Lo, I. Ting Yu, ... 深入研究「Case report: Life-threatening haematochezia from a jejunal leiomyoma」主題。共同形成了獨特的指紋。 ...
Jejunal leiomyosarcoma is a rare variety of malignant small bowel tumor and a clinical presentation with intussusception is ... In this case report, an unusual presentation of jejunal sarcoma and management of liver metastasis with radiofrequency ablation ... However, it is the site of only 6-25% of GI neoplasms and only 2% of GI malignancies [2, 6]. Leiomyosarcoma is the fourth most ... Samaiya, A., Deo, S.S., Thulkar, S. et al. An unusual presentation of a malignant jejunal tumor and a different management ...
Jejunal neuroendocrine tumor metastasis to the testis is extremely rare. We present the case of a 61-year-old man with a ... Testicular neuroendocrine tumors account for less than 1% of all testicular neoplasms. They may present as primary testicular ... Testicular Metastasis of Jejunal Neuroendocrine Tumor on 68Ga-DOTATATE PET/CT. ... jejunal neuroendocrine tumor and metastases to bilateral testicles revealed on Gallium-68-DOTATATE positron emission tomography ...
Jejunal Cancer use Jejunal Neoplasms Jejunal Cancers use Jejunal Neoplasms Jejunal Disease use Jejunal Diseases ...
We report a case of jejunal leiomyosarcoma with intestinal intussusception at the angle of Treitz that was successfully treated ... True smooth muscle neoplasms of the gastrointestinal tract: morphological spectrum and classification in a series of 85 cases ... a Tumor was a white solid mass (10 × 8 × 5 cm in size) located throughout the jejunal wall. b Tumor grew by engulfing the ... Macroscopy of the resected tumor revealed a white solid mass with a size of 10 × 8 × 5 cm located throughout the jejunal wall ( ...
Perforated Jejunal Gastrointestinal Stromal Tumor(GIST) Presenting as Acute Abdomen: A Rare Presentation. Abstract- ... Keywords: Gastrointestinal Stromal Tumors (GIST), Neoplasms, Gastrointestinal system. Click here to Download Full Paper. ... Gastrointestinal stromal tumors (GIST) are rare neoplasms of the gastrointestinal system. A case of 40 year old man having ...
  • Jejunal leiomyosarcoma is a rare variety of malignant small bowel tumor and a clinical presentation with intussusception is unusual. (biomedcentral.com)
  • We report a case of jejunal leiomyosarcoma with intestinal intussusception at the angle of Treitz that was successfully treated with laparoscopic resection followed by intracorporeal reconstruction using a delta-shaped anastomosis. (springeropen.com)
  • We report a case of a middle colic artery originating from the gastroduodenal artery found during a pancreaticoduodenectomy for a pancreatic cystic mucinous neoplasm. (hindawi.com)
  • A follow-up MRI of the abdomen characterized the lesion as an intraductal pancreatic mucinous neoplasm. (hindawi.com)
  • Conclusions: Free jejunal grafts in larynx-preserving surgery can be performed safely and reliably in patients with low cervical esophageal carcinomas and in selected patients with high tumors involving the hypopharynx. (elsevierpure.com)
  • Abstract- Gastrointestinal stromal tumors (GIST) are rare neoplasms of the gastrointestinal system. (adpublications.org)
  • Hepaticojejunostomy (HJS) is an essential component of many surgical procedures, including pancreaticoduodenectomy for benign and malignant neoplasms, resection of bile duct tumors, liver transplantation, palliative treatment for unresectable obstructive tumors, and surgical procedures for chronic pancreatitis or choledocholithiasis [ 1 ]. (mdpi.com)
  • Primary tumors of the small bowel (SB) are rare, representing approximately 1% to 3% of all primary GI neoplasms. (unibo.it)
  • In this case report, an unusual presentation of jejunal sarcoma and management of liver metastasis with radiofrequency ablation (RFA) is discussed. (biomedcentral.com)
  • He underwent an en bloc resection, and pathological findings concluded to a metastasis of a pulmonary combined small cell carcinoma and adenocarcinoma. (hindawi.com)
  • However, intussusception due to a jejunal metastasis of combined lung cancer is extremely rare [ 3 ]. (hindawi.com)
  • In this present case, we report the observation of a patient who presented with an acute intestinal intussusception caused by a jejunal metastasis of pulmonary combined small cell carcinoma and adenocarcinoma and we present a review of the literature. (hindawi.com)
  • A well differentiated, low grade neuroendocrine neoplasm (carcinoid tumor) that arises from the jejunum. (nih.gov)
  • Operative findings revealed an intussuscepted proximal jejunum loop 12 cm distal to duodeno-jejunal flexure and a vascular polypoidal growth measuring 6.5 × 5 × 3.5 cms on serosal surface of jejunum. (biomedcentral.com)
  • Pancreatic Gastrinoma, Gastrointestinal Stromal Tumor (GIST), Pheochromocytoma, and Hürthle Cell Neoplasm in a Patient with Neurofibromatosis Type 1: A Case Report and Literature Review. (nih.gov)
  • Gastric gastrointestinal stromal tumor (GIST) en face. (medscape.com)
  • The paraganglioma-jejunal GIST combination may be the harbinger of a rare genetic syndrome, a variant of the Carney triad or the paraganglioma-gastric stromal sarcoma syndrome, or be coincidental. (elsevierpure.com)
  • 2 Moreover, up to 10% of patients with intraductal papillary mucinous neoplasms (IPMNs), which are pre-malignant lesions, may be initially incorrectly diagnosed with CP. (practicalgastro.com)
  • Objectives/Hypothesis: To examine the efficacy and safety of free jejunal transfer after larynx-preserving esophagectomy in patients with cervical esophageal carcinoma, especially with a high tumor involving the hypopharynx. (elsevierpure.com)
  • Study Design: A retrospective analysis of patients with cervical esophageal carcinoma who underwent free jejunal transfer after larynx-preserving esophagectomy. (elsevierpure.com)
  • Methods: The subjects were 32 patients who underwent larynx-preserving cervical esophagectomy and microvascular jejunal transfer. (elsevierpure.com)
  • Patients who have undergone gastro-jejunal bypass, esophagectomy, or total gastrectomy will be excluded. (knowcancer.com)
  • In these cases, reconstruction was performed using two different microvascular methods: double-pedicle jejunal free flap and supercharged ileocolic interposition graft. (e-acfs.org)
  • Here, we report cases of esophagogastric reconstruction with limited alternative options after the failure of transverse and left colon interposition, for which two different microvascular methods were used: double-pedicle jejunal free flap and supercharged ileocolic interposition. (e-acfs.org)
  • Histologically heterotopic pancreatic tissue is not a true neoplasm but rather a hamartoma of fat glandular tissue with pancreatic acinar formation and duct development [ 8 ]. (biomedcentral.com)
  • Jejunal Neoplasms" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings) . (uams.edu)
  • Five years after gastric bypass, due to ongoing epigastric pain complaints, abdominal CT and MRI were repeated, with subsequent diagnosis of a 4.5 cm of greater diameter subserosal neoplasm in the antrum (Figure 1 B). (biomedcentral.com)
  • To salvage the remnant colon conduit, jejunal free flap reconstruction was planned. (e-acfs.org)
  • Small-bowel capsule endoscopy (SBCE) is a noninvasive and well tolerated procedure that allows direct visualization of the SB mucosa, with a detection rate for neoplasm ranging from 1.6% to 11.5% in procedures performed for any indication. (unibo.it)
  • This graph shows the total number of publications written about "Jejunal Neoplasms" by people in UAMS Profiles by year, and whether "Jejunal Neoplasms" was a major or minor topic of these publications. (uams.edu)
  • Below are the most recent publications written about "Jejunal Neoplasms" by people in Profiles over the past ten years. (uams.edu)
  • Malignant neoplasms show a greater degree of anaplasia and have the properties of invasion and metastasis, compared to benign neoplasms . (lookformedical.com)
  • Gastrointestinal stromal tumors (GISTs) are the most common mesenchymal tumors in the gastrointestinal (GI) tract, but are the least common of small intestinal malignant neoplasms. (gastrores.org)
  • History of malignant neoplasms in the last 5 years before the screening. (who.int)
  • 14. [Stapled esophago-jejunal anastomosis after total gastrectomy in gastric neoplasm]. (nih.gov)
  • Abstract Objectives: Based on establishing the animal model of hepatic jejunal anastomosis, the degree of anastomosis solidity, histological characteristics, postoperative complications were investigated after hepatic jejunal anastomosis. (jscimedcentral.com)
  • The search might begin with Breast Neoplasms, but it is seen after viewing the hierarchy that the more specific Descriptor Breast Neoplasms, Male is wanted. (nih.gov)
  • For example, the subject of jejunal enteritis is expressed by the use of the Descriptors Jejunum and Enteritis , so in PubMed a searcher would combine these Descriptors in a query. (nih.gov)
  • Gastric gastrointestinal stromal tumor (GIST) en face. (medscape.com)
  • Diagnostic features and management options for duodenal neuroendocrine neoplasms: a retrospective, multi-centre study. (nih.gov)
  • Clip-guided local duodenectomy for safe and minimal local resection of nonampullary duodenal neoplasms. (nih.gov)
  • or (4) duodenal-jejunal bypass sleeve, if the sleeve was removed more than 1 year before the screening. (who.int)
  • Educational goals: Highlight epidemiology, clinical presentation, radiographic findings, and treatment for common neonatal obstructions considered high in the intestinal tract including malrotation with midgut volvulus, duodenal atresia, duodenal web, annular pancreas, and proximal jejunal atresia. (abstractarchives.com)
  • Cr(VI) exposure resulted in increased incidences of rare neoplasms of the squamous epithelium that lines the oral cavity (oral mucosa and tongue) in male and female rats, and of the epithelium lining the small intestine in male and female mice. (nih.gov)
  • A well differentiated, low grade neuroendocrine neoplasm (carcinoid tumor) that arises from the small or large intestine. (nih.gov)
  • Metastatic Jejunal Renal Cell Carcinoma Intussusception Presenting as " by Emad Elmusa, Muhammad Waleed Raza et al. (hcahealthcare.com)
  • Elmusa E, Raza M, Hamza A, Tahir Khokhar H, Butt M. Metastatic Jejunal Renal Cell Carcinoma Intussusception Presenting as Melena. (hcahealthcare.com)
  • Within an hour after an apparently uncomplicated colonoscopy, he developed an acute abdomen secondary to a jejunal intussusception, which led to a laparoscopic small bowel resection and the diagnosis of a jejunal GIST. (gastrores.org)
  • This case illustrates the complex presentation and diagnostic difficulty of a jejunal GIST causing obscure, overt GI bleeding and this is the first reported case of a jejunal intussusception following colonoscopy. (gastrores.org)
  • Investigation with push enteroscopy revealed a jejunal mass, and further evaluation with CT showed small bowel intussusception. (hcahealthcare.com)
  • Wedge resection with primary closure is a surgical procedure that can be used to treat low malignant potential neoplasms of the duodenum and avoid extensive surgery, with significant morbidity and possible mortality, such as pancreatoduodenectomy. (wjgnet.com)
  • The aim of this paper was to present indication, srugical technique, and early results of jejunal implement at the distal part of esophagus reconstructed with colon. (home.pl)
  • When placing a jejunal extension, clips may secure the distal end of the tube to reduce the risk of retrograde migration. (friendsofendoscopy.org)
  • Incidental mesonephric remnant hyperplasia of the jejunal mesentery: A diagnostic challenge. (nih.gov)
  • Jejunal implement - the another method of gastroesophageal reflux treatment after esophageal reconstruction with colon. (home.pl)
  • Material and methods: During las two-year period 5 patietns, aged from 9 months to 11 years, underwent implementation of jejunal segment simultaneously or a year later after esophageal reconstruction with colon interposition. (home.pl)
  • Abstract Multiple Myeloma (MM) is a malignant B neoplasm that can be characterized as a plasma cell dyscrasia in the bone marrow. (jscimedcentral.com)
  • Postmortem photomicrographs of an impression smear (A) and tissue section (B) of the jejunal wall mass described in Figure 1 . (avma.org)
  • Stewart DR, Best AF, Williams GM et al (2019) Neoplasm risk among individuals with a pathogenic germline variant in DICER1 . (springer.com)
  • Histopathology confirmed that the jejunal mass was metastatic RCC. (hcahealthcare.com)
  • The neoplasms may be histologically the same or different, and may be found in the same or different sites. (lookformedical.com)
  • No article was found for Jejunal Neoplasms and TP53[original query] . (cdc.gov)
  • Gonadal neoplasm in children with female phenotype and Y chromosome in karyotype. (home.pl)
  • The indication of delayed use of jejunal implement was extensive and deep inflammation of mucose of interposed colon, resulted in intensive bleeding, which need repeated blood transfusion. (home.pl)