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sarcoidosis/diarrea
L'enllaç es desa al porta-retalls
Pàgina 1 des de 36 resultats
[Diarrhea, protein-losing enteropathy and sarcoidosis].
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A case of inactive sarcoidosis associated with protein-losing enteropathy, severe hypoalbuminemia and diarrhea is reported. 99mTc-labeled human serum albumin was performed to show protein loss. There was no abnormal upper gastrointestinal mucosa as shown by peroral duodenal and jejunal biopsies.
Isolated Gastrointestinal Sarcoidosis Involving Multiple Gastrointestinal Sites Presenting as Chronic Diarrhea.
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Sarcoidosis is a chronic and systemic disorder characterized by the formation of non-caseating granulomas. Very few cases of isolated gastrointestinal sarcoidosis have been reported, and even fewer, if any, report gastrointestinal sarcoidosis within multiple gastrointestinal sites concomitantly. We
Deafness, dysesthesia, depression, diarrhea, dropsy, and death: the case for sarcoidosis in Ludwig van Beethoven.
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[Massive chronic diarrhea. 56-year-old patient with sarcoidosis and high grade pleomorphic T-cell non-Hodgkin lymphoma].
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[Sarcoidosis in children with digestive manifestations].
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BACKGROUND
Gastric involvement is the least rare among digestive localizations of sarcoidosis, as well in adults as in children. When it is to be seen at the beginning of the disease, it may cause difficulties in the diagnostic, especially with Crohn's disease.
METHODS
Gastric ulcers were detected
Interferon-alpha-induced sarcoidosis in a patient being treated for hepatitis C.
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METHODS
Female, 43 FINAL DIAGNOSIS: -
METHODS
Diarrhea • generalized weakness • headache • lightheadedness • nausea • rash • short of breath • vomiting
METHODS
- Clinical Procedure: - Specialty: Pulmonology.
OBJECTIVE
Rare diseae.
BACKGROUND
IFN-alpha-2b in combination with ribavirin is now the
Sarcoidosis of the stomach and rectum.
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A patient, whose symptoms included epigastric pain, nausea and vomiting relieved with antacids but with no history of diarrhea or constipation, was found to have generalized sarcoidosis involving his lungs, liver, lymph nodes, skin, stomach and rectum. Because sarcoidosis rarely involves the
A case of sarcoidosis with isolated hepatosplenic onset and development of inflammatory bowel disease during recovery stage.
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Sarcoidosis is a systemic disease characterized by an immune-mediated disorder, which leads to the development of non-caseating granulomas in the involved organs. More than 90% of patients with sarcoidosis present lungs and lymphatic system involvement at onset, while less than 10% has an isolated
[Digestive sites disclosing sarcoidosis].
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We report two cases of gastrointestinal sarcoidosis. One patient had a gastric involvement, the other a duodenal and ileum involvement. The two patients had the same symptoms, including diarrhea, vomiting, abdominal pain and weight loss. Endoscopic examination revealed only an erythematous gastritis
Persistent diarrhea.
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A 63-year-old man presented with massive diarrhea and weight loss. This was preceded by nonspecific symptoms for three years, which resembled sarcoidosis. By duodenal biopsy, the diagnosis of Whipples disease was confirmed. Antibiotic treatment resulted in rapid and complete disappearance of signs
[Sarcoidosis of the large intestine].
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A 68-years old female patient suffering over a period of several weeks from fatigue, weight loss, recurrent diarrheas and mild fever was admitted in our clinic. A few months ago, sarcoidosis of a cervical lymph node had been diagnosed and had been treated with steroids. During the present admission,
[Sarcoidosis and Whipple's disease: an association or a relationship?].
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Whipple's disease is a rare, systemic disorder characterized by arthritis, serositis, diarrhea, malabsorption, lymphadenopathies, weight loss, fever, cutaneous hyperpigmentation and central and peripheral nervous system disorders. There are approximately 60 published cases with pulmonary
Systemic elastolytic granulomatosis with cutaneous, ocular, lymph nodal, and intestinal involvement. Spectrum of annular elastolytic giant cell granuloma and sarcoidosis.
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A 15-year-old Japanese girl had widespread annular serpiginous erythematous plaques, bilateral granulomatous uveitis, bloody diarrhea, and seronegative arthralgia. She also had anemia and leukopenia. The histopathologic findings were compatible with those of annular elastolytic giant cell granuloma.
Colon Sarcoidosis Mimicking Cancer at 18F-FDG PET/CT.
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This 68-year-old woman with a 9-year history of skin sarcoidosis presented with abdominal pain, bloating, and diarrhea. Following positive occult fecal blood, a diagnosis of ascending colon sarcoidosis was pathologically confirmed after colonoscopy. FDG PET/CT was performed for sarcoid staging, and
Unusual presentation of a colonic sarcoidosis.
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Sarcoidosis is a multisystemic disorder of unknown cause that affects almost every tissue in the body. Colon is an extremely rare location of this disease. Clinical presentation, endoscopic appearances, and radiologic findings are not specific and may mimic much other affection. We report the case
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