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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


Subject(s)
Humans , Male , Autoimmune Diseases , Polyendocrinopathies, Autoimmune , Vitiligo , Protein-Losing Enteropathies , Duodenum/pathology
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