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[Congenital intestinal lymphangiectasia].

Identifieur interne : 002650 ( PubMed/Corpus ); précédent : 002649; suivant : 002651

[Congenital intestinal lymphangiectasia].

Auteurs : Dugan D J Popovi ; Milan Spuran ; Tamara Alempijevi ; Miodrag Krsti ; Srdjan Djuranovi ; Nada Kovacevi ; Svetozar Damnjanovi ; Marjan Micev

Source :

RBID : pubmed:21526555

English descriptors

Abstract

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.

PubMed: 21526555

Links to Exploration step

pubmed:21526555

Le document en format XML

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<name sortKey="Popovi, Dugan D J" sort="Popovi, Dugan D J" uniqKey="Popovi D" first="Dugan D J" last="Popovi">Dugan D J Popovi</name>
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<nlm:affiliation>Klinicki centar Srbije, Sluzba za patohistologiju, Beograd, Srbija. dr.popovic@sezampro.rs</nlm:affiliation>
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<name sortKey="Spuran, Milan" sort="Spuran, Milan" uniqKey="Spuran M" first="Milan" last="Spuran">Milan Spuran</name>
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<name sortKey="Alempijevi, Tamara" sort="Alempijevi, Tamara" uniqKey="Alempijevi T" first="Tamara" last="Alempijevi">Tamara Alempijevi</name>
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<name sortKey="Krsti, Miodrag" sort="Krsti, Miodrag" uniqKey="Krsti M" first="Miodrag" last="Krsti">Miodrag Krsti</name>
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<name sortKey="Djuranovi, Srdjan" sort="Djuranovi, Srdjan" uniqKey="Djuranovi S" first="Srdjan" last="Djuranovi">Srdjan Djuranovi</name>
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<name sortKey="Kovacevi, Nada" sort="Kovacevi, Nada" uniqKey="Kovacevi N" first="Nada" last="Kovacevi">Nada Kovacevi</name>
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<name sortKey="Damnjanovi, Svetozar" sort="Damnjanovi, Svetozar" uniqKey="Damnjanovi S" first="Svetozar" last="Damnjanovi">Svetozar Damnjanovi</name>
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<name sortKey="Micev, Marjan" sort="Micev, Marjan" uniqKey="Micev M" first="Marjan" last="Micev">Marjan Micev</name>
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<name sortKey="Spuran, Milan" sort="Spuran, Milan" uniqKey="Spuran M" first="Milan" last="Spuran">Milan Spuran</name>
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<name sortKey="Krsti, Miodrag" sort="Krsti, Miodrag" uniqKey="Krsti M" first="Miodrag" last="Krsti">Miodrag Krsti</name>
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<name sortKey="Djuranovi, Srdjan" sort="Djuranovi, Srdjan" uniqKey="Djuranovi S" first="Srdjan" last="Djuranovi">Srdjan Djuranovi</name>
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<name sortKey="Kovacevi, Nada" sort="Kovacevi, Nada" uniqKey="Kovacevi N" first="Nada" last="Kovacevi">Nada Kovacevi</name>
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<name sortKey="Damnjanovi, Svetozar" sort="Damnjanovi, Svetozar" uniqKey="Damnjanovi S" first="Svetozar" last="Damnjanovi">Svetozar Damnjanovi</name>
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<term>Lymphangiectasis, Intestinal (diagnosis)</term>
<term>Lymphangiectasis, Intestinal (therapy)</term>
<term>Male</term>
<term>Young Adult</term>
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<keywords scheme="MESH" qualifier="congenital" xml:lang="en">
<term>Lymphangiectasis, Intestinal</term>
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<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en">
<term>Lymphangiectasis, Intestinal</term>
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<keywords scheme="MESH" qualifier="therapy" xml:lang="en">
<term>Lymphangiectasis, Intestinal</term>
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<div type="abstract" xml:lang="en">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.</div>
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<Day>07</Day>
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<Month>06</Month>
<Day>12</Day>
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<Year>2011</Year>
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<Title>Vojnosanitetski pregled</Title>
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<ArticleTitle>[Congenital intestinal lymphangiectasia].</ArticleTitle>
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<AbstractText Label="BACKGROUND" NlmCategory="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.</AbstractText>
<AbstractText Label="CASE REPORT" NlmCategory="METHODS">A 19-year old male patient was hospitalized due to diarrhea, abdominal swelling, weariness and fatigue. Physical examination revealed growth impairment, ascites, and lymphedema of the right hand and forearm. Laboratory assessment indicated iron deficiency anaemia, lymphopenia, malabsorption, inflammatory syndrome, and urinary infection. Enteroscopy and video capsule endoscopy demonstrated dilated lymphatic vessels in the small intestine. The diagnosis was confirmed by intestinal biopsy. The patient was put on high-protein diet containing medium-chain fatty acids, somatotropin and supportive therapy.</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">Congenital intestinal lymphangiectasia is a rare disease, usually diagnosed in childhood. Early recognition of the disease and adequate treatment can prevent development of various complications.</AbstractText>
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<LastName>Popović</LastName>
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   |area=    LymphedemaV1
   |flux=    PubMed
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   |clé=     pubmed:21526555
   |texte=   [Congenital intestinal lymphangiectasia].
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