Mediterranean Journal of Hematology and Infectious Diseases (Aug 2014)

Hepatosplenic Gamma Delta T cell Lymphoma in a Young Male with Visceral Leishmaniasis

  • Deepti Mutreja,
  • Mrinalini Kotru,
  • Mukul Aggarwal,
  • Narendra Tejwani,
  • Rahul Kumar Sharma,
  • HaraPrasad Pati

Journal volume & issue
Vol. 1

Abstract

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Hepatosplenic gamma delta T-cell lymphoma (HSTCL) is a rare peripheral T-cell lymphoma of cytotoxic T-cell origin with an aggressive clinical course. It is characterized by hepatosplenomegaly without significant lymphadenopathy, with clinically significant cytopenias. Chronic immunosuppression has been proposed as a possible pathogenetic mechanism in HSTCL. No association of HSTCL with visceral leishmaniasis has been described in the past. We describe a case of an adolescent male patient with HSTCL with leukemic presentation, who was diagnosed to have visceral leishmaniasis, nine months prior to presentation at our centre.

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