Hemophagocytic syndrome and acute pancreatitis in acute systemic lupus erythematosus

被引：0

作者：

Alblewi, Bushra ^{[1
,2
]}

Bukhari, Iqbal A. ^{[1
,2
]}

Hasan, Manal ^{[2
,3
]}

Alzahani, Abdulaziz ^{[1
,2
]}

Bukhari, Raed ^{[2
,3
]}

Bashawri, Layla ^{[2
,4
]}

Al Shawarby, Muhammad ^{[2
,4
]}

机构：

[1] Univ Dammam, Coll Med, Dermatol Dept, Dammam, Saudi Arabia

[2] King Fahd Hosp Univ, Dammam, Saudi Arabia

[3] Univ Dammam, Coll Med, Internal Med Dept, Dammam, Saudi Arabia

[4] Univ Dammam, Coll Med, Pathol Dept, Dammam, Saudi Arabia

来源：

JOURNAL OF DERMATOLOGY DERMATOLOGIC SURGERY-JDDS | 2014年 / 18卷 / 1-2期

关键词：

Hemophagocytic syndrome; Acute systemic lupus erythematosus; Acute pancreatitis;

D O I：

10.1016/j.jdds.2014.03.004

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

Hemophagocytic syndrome (HPS) is characterized by the activation of histiocytes with prominent hemophagocytosis in bone marrow and other reticuloendothelial systems. It has two forms: primary and secondary. The precise pathogenesis of HPS is unclear but a dysregulation of macrophage-lymphocyte interactions with subsequent increases in the levels of both T-cell-derived and macrophagederived cytokines has been suggested. Cardinal symptoms of HPS are prolonged high fever, hepatosplenomegaly, cytopenias, lymphadenopathy and neurological symptoms. In this report, we present a case Systemic Lupus Erythematosus associated with HPS and acute pancreatitis. (C) 2014 Production and hosting by Elsevier B.V.

引用

页码：35 / 37

页数：3

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