2018
DOI: 10.1097/mph.0000000000001178
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Hemophagocytic Lymphohistiocytosis Associated With Visceral Leishmaniasis

Abstract: This is the report of a 2-year-old boy who presented with fever, cytopenia, and splenomegaly. The patient was diagnosed with hemophagocytic lymphohistiocytosis (HLH) and treated with HLH-2004 protocol. Repeated bone marrow aspiration showed amastigotes on follow-up. In endemic countries, visceral leishmaniasis should be considered in the differential diagnosis to avoid chemotherapy toxicity.

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“…Clinicians should distinguish between primary and secondary HPS, and make a clear etiological diagnosis of secondary HPS. The possibility of VL should be considered when diagnosing HPS[ 8 , 9 ]. Treatment measures for secondary HPS should be established according to the primary disease; following treatment appropriate for primary HPS may lead to adverse outcomes.…”
Section: Discussionmentioning
confidence: 99%
“…Clinicians should distinguish between primary and secondary HPS, and make a clear etiological diagnosis of secondary HPS. The possibility of VL should be considered when diagnosing HPS[ 8 , 9 ]. Treatment measures for secondary HPS should be established according to the primary disease; following treatment appropriate for primary HPS may lead to adverse outcomes.…”
Section: Discussionmentioning
confidence: 99%