Castleman's Disease: A Case Report of the Unicentric Type
Author(s) -
Joaquín Gómez-Ramirez,
Myriam Posada,
L. Sanchez-Urdazpal,
Elena MartínPérez,
Lourdes del Campo,
Isabel Ponce García,
Jamie L. Martin,
Eduardo Larrañaga
Publication year - 2012
Publication title -
case reports in surgery
Language(s) - English
Resource type - Journals
eISSN - 2090-6900
pISSN - 2090-6919
DOI - 10.1155/2012/175272
Subject(s) - medicine , hyaline , pathological , disease , lymph node , plasma cell , pathology , presentation (obstetrics) , castleman disease , hyperplasia , lymph , surgery , bone marrow
Castleman's disease, or angiofollicular lymph node hyperplasia, is a relatively rare disorder characterized by the benign proliferation of lymphoid tissue related to the chronic human herpes virus 8 (HHV-8) infection and the human immunodeficiency virus (HIV). Two clinical entities have been described: a unicentric presentation with the disease confined to a single anatomic lymph node and a multicentric presentation characterized by generalized lymphadenopathy and a more aggressive clinical course. Also, three histopathological subtypes have been described: hyaline-vascular, plasma cell, and a mixed variant. Preoperative diagnosis of hyaline-vascular Castleman's disease is difficult, and the definitive result is based on postoperative pathological findings. The gold standard therapy is the complete surgical excision.
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