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International Journal of Health Sciences. 2008; 2 (1): 109-112
in English | IMEMR | ID: emr-133884

ABSTRACT

A 20-year-old male Saudi national presented initially with leucopenia and splenomegaly. The absence of other signs of disease, progressive pancytopenia and normal bone marrow examination posed a diagnostic dilemma as to the cause of hypersplenism. Subsequently, the patient had splenectomy the histopathological appearance of which was non-caseating granuloma. A high level of angiotension converting enzyme [ACE] was found in this patient. Sarcoidosis is a recognized cause of hypersplenism, and though the disease is not yet widely described in this part of the world. It is the most probable diagnosis in this patient


Subject(s)
Humans , Male , Sarcoidosis/diagnosis , Pancytopenia/diagnosis , Splenomegaly , Hypersplenism , Peptidyl-Dipeptidase A , Bone Marrow
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