UNUSUAL CASE OF ADULT HEMOPHAGOCYTIC SYNDROME (CASE REPORT)

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TAMIZIFAR BABAK; SAMADI GOLNAZ; RISMANKARZADEH MARYAM

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Journal Paper

Paper Information

Journal: JOURNAL OF RESEARCH IN MEDICAL SCIENCES (JRMS) Year:2014 | Volume:18 | Issue:2 Page(s): 178-180

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Information Journal Paper

Title

UNUSUAL CASE OF ADULT HEMOPHAGOCYTIC SYNDROME (CASE REPORT)

Author(s)

TAMIZIFAR BABAK | SAMADI GOLNAZ | RISMANKARZADEH MARYAM | Issue Writer Certificate

Keywords

AUTOIMMUNITY

HEMOPHAGOCYTIC SYNDROME

HEMOPHAGOCYTOSIS

SYSTEMIC LUPUS ERYTHEMATOSUS

Abstract

Hemophagocytic syndrome (HPS) is an uncommon manifestation in SYSTEMIC LUPUS ERYTHEMATOSUS (SLE). Clinical features of HPS include fever, pancytopenia, abnormal liver enzyme, hepatosplenomegaly, lymphadenopathy, and coagulation disorder. HPS comprises primary and reactive forms. Herein, we describe a case of untreated SLE with HPS as one of the first manifestations of systemic Lupus.

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APA: Copy

TAMIZIFAR, BABAK, SAMADI, GOLNAZ, & RISMANKARZADEH, MARYAM. (2014). UNUSUAL CASE OF ADULT HEMOPHAGOCYTIC SYNDROME (CASE REPORT). JOURNAL OF RESEARCH IN MEDICAL SCIENCES (JRMS), 18(2), 178-180. SID. https://sid.ir/paper/623994/en

Vancouver: Copy

TAMIZIFAR BABAK, SAMADI GOLNAZ, RISMANKARZADEH MARYAM. UNUSUAL CASE OF ADULT HEMOPHAGOCYTIC SYNDROME (CASE REPORT). JOURNAL OF RESEARCH IN MEDICAL SCIENCES (JRMS)[Internet]. 2014;18(2):178-180. Available from: https://sid.ir/paper/623994/en

IEEE: Copy

BABAK TAMIZIFAR, GOLNAZ SAMADI, and MARYAM RISMANKARZADEH, “UNUSUAL CASE OF ADULT HEMOPHAGOCYTIC SYNDROME (CASE REPORT),” JOURNAL OF RESEARCH IN MEDICAL SCIENCES (JRMS), vol. 18, no. 2, pp. 178–180, 2014, [Online]. Available: https://sid.ir/paper/623994/en

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