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Hypoplasia of the spleen: Review of pathogenesis, diagnosis, and potential clinical implications
Author(s) -
Iswanto Sucandy,
Harsha V. Polavarapu,
Christopher M. Pezzi
Publication year - 2015
Publication title -
north american journal of medical sciences
Language(s) - English
Resource type - Journals
eISSN - 2250-1541
pISSN - 1947-2714
DOI - 10.4103/1947-2714.163645
Subject(s) - medicine , pathogenesis , pathology , hypoplasia , spleen , bioinformatics , anatomy , immunology , biology
Splenic aplasia is seen when the spleen is congenitally absent, has been surgically removed, or becomes atrophic secondary to episodes of arterial/venous occlusion, which result in splenic infarction. This rare condition is caused by a heterogenous group of diseases, which may present a wide spectrum of clinical manifestations. Splenic hypoplasia is defined as reduction in splenic mass and or functions caused by incomplete splenic development or secondary parenchymal involution. Splenic infarction may be clinically silent and only discovered incidentally during abdominal exploration for other conditions.

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