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[Primary intestinal lymphangiectasia in a patient with polyglandular autoimmune disease]
JBMS-Journal of the Bahrain Medical Society. 2009; 21 (4): 356-358
in English | IMEMR | ID: emr-101864
ABSTRACT
Primary intestinal lymphangiectasia is a rare disorder that is not commonly associated with autoimmune phenomena. We report a case of a 29-year-old man with primary lymphangiectasia who additionally had vitiligo, autoimmune hypothyroidism, hypogonadism, and pernicious anemia. We speculate that autoimmunity may play a role in the pathogenesis of primary intestinal lymphangiectasia
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Index: IMEMR (Eastern Mediterranean) Main subject: Protein-Losing Enteropathies / Autoimmune Diseases / Vitiligo / Polyendocrinopathies, Autoimmune / Duodenum Type of study: Case report Limits: Humans / Male Language: English Journal: J. Bahrain Med. Soc. Year: 2009

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Index: IMEMR (Eastern Mediterranean) Main subject: Protein-Losing Enteropathies / Autoimmune Diseases / Vitiligo / Polyendocrinopathies, Autoimmune / Duodenum Type of study: Case report Limits: Humans / Male Language: English Journal: J. Bahrain Med. Soc. Year: 2009