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Visceral leishmaniasis in an Afghan woman with systemic lupus erythematosus
Author(s) -
Sadia Sultan,
Syed Mohammad Irfan
Publication year - 2014
Publication title -
blood research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.422
H-Index - 22
eISSN - 2288-0011
pISSN - 2287-979X
DOI - 10.5045/br.2014.49.4.215
Subject(s) - medicine , visceral leishmaniasis , afghan , systemic lupus , dermatology , leishmaniasis , systemic lupus erythematosus , immunology , disease , philosophy , theology
which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. A 35-year-old Afghan woman with systemic lupus erythematosus for 3 years had been on immunosuppressive and low-dose steroid therapy for 1 year. She presented with fever, abdominal pain, and excessive sweating for 2 months. hands were noted. Laboratory tests revealed hemoglobin level of 7.9 g/dL, white blood cell counts of 1.0×10 9 /L, absolute neutrophil counts of 0.4×10 9 /L, and platelet counts of 56×10 9 /L. A peripheral blood smear revealed polychromasia, spherocytes, and nucleated red blood cells. In the bone marrow, abundant intracellular (A) and extracellular amastigotes appearing as single cells (B) or in small clusters (C) were detected. Numerous macrophages loaded with amastigotes were seen (D and E) in a trephine biopsy. The patient was treated with stibogluconate and responded well to therapy. Peripheral counts were normalized after 2 weeks, visceromegaly was resolved after 3 weeks, and no amastigotes were found in the bone marrow at the end of treatment. Physicians should be aware of the possibility of an underlying parasitic infestation in immunocompromised patients, as cytopenia may not always be due to primary disease or a consequence of immunosuppressive therapy.

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