与噬血细胞综合征及孤立性脾紫癜相关的非创伤性脾破裂。病例报告。

Atraumatic rupture of the spleen associated with hemophagocytic syndrome and isolated splenic peliosis. Case report.

作者信息

Etzion Yoram, Benharroch Daniel, Saidel Marcello, Riesenberg Klaris, Gilad Jacob, Schlaeffer Francisc

机构信息

Department of Internal Medicine E, Soroka University Medical Center and Faculty for Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.

出版信息

APMIS. 2005 Jul-Aug;113(7-8):555-7. doi: 10.1111/j.1600-0463.2005.apm_165.x.

DOI:10.1111/j.1600-0463.2005.apm_165.x

PMID:16086827

Abstract

Atraumatic rupture of the spleen is an uncommon condition that may be associated with various etiologies. The hemophagocytic syndrome (HS) and isolated splenic peliosis are two rare conditions, each of which has previously been described in association with splenic rupture. We describe a unique case of atraumatic splenic rupture in which concurrent HS and splenic peliosis were diagnosed following splenectomy. Given that both these rare conditions have probably caused the splenic rupture, a possible association between these entities is discussed.

摘要

非创伤性脾破裂是一种罕见的病症，可能与多种病因相关。噬血细胞综合征（HS）和孤立性脾紫癜是两种罕见的病症，此前均有与脾破裂相关的报道。我们描述了一例独特的非创伤性脾破裂病例，在脾切除术后诊断出同时存在HS和脾紫癜。鉴于这两种罕见病症可能均导致了脾破裂，本文对这些病症之间可能存在的关联进行了讨论。