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Malakoplakia is a rare inflammatory condition seen in transplant patients. There are two previously reported cases of malakoplakia involving the gastrointestinal tract in liver transplant patients. The present paper reports a case of colonic malakoplakia in a 58-year-old woman, a liver transplant
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We are presenting the case of a 13 year-old male child who was hospitalized at INSN, with generalized edema, chronic diarrhea and hematoquezia. Biopsy studies of the intestine established the diagnosis of Malacoplakia. Despite of the treatment the clinical evolution didn't improve. A review of
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We describe the first published case of malakoplakia in a dual stem-cell and cardiac transplant recipient. In the two months following cardiac transplantation, our patient developed persistent diarrhea and recurrent E. coli bacteraemia. Biopsies obtained from areas of colonic thickening revealed
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We report on malakoplakia of the colon observed in a six month old girl in a setting of severe combined immunodeficiency (SCID) and a malformational syndrome termed CHARGE association. By the age of six months, hemorrhagic diarrhea had developed, and multiple ulcers were seen at colonoscopy. The
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Malacoplakia is an uncommon, pathologically distinct, granulomatous disease most frequently found in the urinary tract. Malacoplakia of the colon may cause abdominal pain, diarrhea, rectal bleeding, and fever. Radiographic features are variable and include polyps, bulky masses, mucosal ulcerations,
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We studied 5 children with intestinal malakoplakia who were seen during a period of 10 years. Four were male and one female. The main clinical manifestations were: chronic bloody and mucous diarrhea, abdominal pain and polypoid masses detected by rectal maneuver. Either the radiological study as
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Malacoplakia is a form of chronic granulomatous inflammatory reaction that rarely affects the pediatric age group. The gastrointestinal system is the second most common site for the occurrence of malacoplakia. We report the case of a 9-year-old girl who was hospitalized for abdominal pain, chronic
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Description of a case of malacoplakia involving the ascending colon and appendix in a 11-year-old boy with history of severe diarrhea. The lesions were studied by light and electron microscopy. They were composed of proliferation of histiocytes with the typical cytoplasmic inclusions known as
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METHODS
A 45 year old man was admitted to our hospital because of fever, loss of appetite, and deterioration of general health. For two weeks the patient suffered from diarrhea which had resulted in moderate volume depletion. In addition, he complained of bilateral flank pain at the time of
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Four children, whose ages ranged from 1 to 13 years, with malacoplakia of the gastrointestinal tract were treated at King Faisal Specialist Hospital between 1979 and 1983. All patients had either a preceding or a coexisting chronic illness. In one patient, malacoplakia was an incidental finding,
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BACKGROUND
Malacoplakia, a chronic granulomatous disease, rarely involves the digestive tube and, when it does, takes on a pseudotumoral aspect.
METHODS
A 37 year-old man was hospitalized for chronic diarrhea that had progressed over 15 years. He exhibited an edematous-ascitic syndrome and bilateral
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Malakoplakia is an inflammatory process related to defective macrophage response to bacterial infection. To further characterize the clinicopathologic manifestations of gastrointestinal malakoplakia, 26 cases were identified from 6 institutions. Hematoxylin and eosin-stained slides and available
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Malakoplakia is a rare granulomatous disease that occurs commonly in the urinary tract and secondarily in the gastrointestinal tract. Most reported cases of malakoplakia are associated with immunosuppressive diseases or chronic prolonged illness. Here, we report a rare case of malakoplakia in a
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