Gastrointestinal Cryptococcosis Associated with Intestinal Lymphangiectasia

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Intestinal Lymphangiectasia

History A three year old boy presented with tetanus who additionally suffered from nonbloody diarrhea. Physical examination showed bilateral edema of the lower limbs. Laboratory data showed iron deficiency anemia, hypoalbuminemia, hypocalcaemia and hypogammaglobulinemia. Stool culture was negative for bacteria however fat droplets were detected in the patient’s stool. Endoscopic examination rev...

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Intestinal lymphangiectasia.

A 2 year and 11 month old boy presented in December 1994 with a history of recurrent episodes of generalized swelling of the body and loose stools for two years. He had been treated with plasma transfusion and antituberculous treatment in the past. He was the only child to his non-consanguineous parents. At birth, he was noticed to have facial asymmetry. He was breastfed for one year and at adm...

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Intestinal lymphangiectasia associated with angiofollicular lymph node hyperplasia (Castleman's disease).

A patient presenting with predominantly gastrointestinal symptoms and a history of myocardial infarction was found to have ascites, hepatosplenomegaly, para-aortic lymphadenopathy, thrombocytosis, and a paraproteinaemia. A jejunal biopsy specimen showed lymphangiectasia and histology of the spleen and lymph nodes showed angiofollicular hyperplasia or Castleman's disease of the hyaline vascular ...

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Intestinal lymphangiectasia associated with recurrence of histiocytosis X.

Intestinal lymphangiectasia may occur as a primary congenital disorder or a secondary disorder. Secondary lymphangiectasia could be associated with diseases such as abdominal carcinoma, retroperitoneal fibrosis or chronic pancreatitis. This is the first reported case of intestinal lymphangiectasia associated with recurrent histiocytosis X. This case report illustrates the need for more prospect...

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[Congenital intestinal lymphangiectasia].

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ژورنال

عنوان ژورنال: Case Reports in Medicine

سال: 2020

ISSN: 1687-9627,1687-9635

DOI: 10.1155/2020/7870154