Congenital intestinal lymphangiectasia

نویسندگان
چکیده

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منابع مشابه

[Congenital intestinal lymphangiectasia].

BACKGROUND Congenital intestinal lymphangiectasia is a disease which leads to protein losing enteropathy. Tortuous, dilated lymphatic vessels in the intestinal wall and mesenterium are typical features of the disease. Clinical manifestations include malabsorption, diarrhea, steatorrhea, edema and effusions. Specific diet and medication are required for disease control. CASE REPORT A 19-year o...

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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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Congenital pulmonary lymphangiectasia

Congenital pulmonary lymphangiectasia (PL) is a rare developmental disorder involving the lung, and characterized by pulmonary subpleural, interlobar, perivascular and peribronchial lymphatic dilatation. The prevalence is unknown. PL presents at birth with severe respiratory distress, tachypnea and cyanosis, with a very high mortality rate at or within a few hours of birth. Most reported cases ...

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Primary intestinal lymphangiectasia.

Primary intestinal lymphangiectasia (PIL) is a rare disease of intestinal lymphatics presenting with hypoproteinemia, bilateral lower limb edema, ascites, and protein losing enteropathy. We report a series of 4 children from Chennai, India presenting with anasarca, recurrent diarrhea, hypoproteinemia and confirmatory features of PIL on endoscopy and histopathology.

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ژورنال

عنوان ژورنال: Military Medical and Pharmaceutical Journal of Serbia

سال: 2011

ISSN: 0042-8450,2406-0720

DOI: 10.2298/vsp1103270p