Unusual Case of Adult Hemophagocytic Syndrome

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Unusual Case of Adult Hemophagocytic Syndrome

Tamizifar B¹ ; Samadi G² ; Rismankarzadeh M³

Source: Journal of Research in Medical Sciences Published:2014

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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Style	Citing Format
MLA	Tamizifar B, Samadi G, Rismankarzadeh M. "Unusual Case of Adult Hemophagocytic Syndrome." Journal of Research in Medical Sciences, vol. 19, no. 2, 2014, pp. 178-180.
APA	Tamizifar B, Samadi G, Rismankarzadeh M (2014). Unusual Case of Adult Hemophagocytic Syndrome. Journal of Research in Medical Sciences, 19(2), 178-180.
Chicago	Tamizifar B, Samadi G, Rismankarzadeh M. "Unusual Case of Adult Hemophagocytic Syndrome." Journal of Research in Medical Sciences 19, no. 2 (2014): 178-180.
Harvard	Tamizifar B, Samadi G, Rismankarzadeh M (2014) 'Unusual Case of Adult Hemophagocytic Syndrome', Journal of Research in Medical Sciences, 19(2), pp. 178-180.
Vancouver	Tamizifar B, Samadi G, Rismankarzadeh M. Unusual Case of Adult Hemophagocytic Syndrome. Journal of Research in Medical Sciences. 2014;19(2):178-180.
BibTex	@article{ author = {Tamizifar B and Samadi G and Rismankarzadeh M}, title = {Unusual Case of Adult Hemophagocytic Syndrome}, journal = {Journal of Research in Medical Sciences}, volume = {19}, number = {2}, pages = {178-180}, year = {2014} }
RIS	TY - JOUR AU - Tamizifar B AU - Samadi G AU - Rismankarzadeh M TI - Unusual Case of Adult Hemophagocytic Syndrome JO - Journal of Research in Medical Sciences VL - 19 IS - 2 SP - 178 EP - 180 PY - 2014 ER -

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