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Systemic leishmaniasis mimicking malignant histiocytosis
Author(s) -
Matzner Yaacov,
Behar Albert,
Beeri Elliot,
Gunders Ar E.,
Hershko Chaim
Publication year - 1979
Publication title -
cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.052
H-Index - 304
eISSN - 1097-0142
pISSN - 0008-543X
DOI - 10.1002/1097-0142(197901)43:1<398::aid-cncr2820430156>3.0.co;2-3
Subject(s) - pancytopenia , medicine , malignant histiocytosis , visceral leishmaniasis , sodium stibogluconate , pathology , leishmaniasis , histiocytosis , lymph , differential diagnosis , spleen , fever of unknown origin , bone marrow , dermatology , immunology , histiocyte , disease
A 22‐year‐old man with fever, hepato‐splenomegaly and severe pancytopenia is described in whom the histologic features of the spleen, liver and lymph nodes were consistent with malignant histiocytosis. Characteristic Leishman‐Donovan bodies were demonstrated on a bone marrow aspirate, and the diagnosis of visceral leishmaniasis was confirmed by culturing the flagellated forms of the pathogen, and by an excellent response to sodium stibogluconate. In view of the similarity in clinical and histologic appearance, visceral leishmaniasis must be considered in the differential diagnosis of malignant histiocytosis in geographic areas where leishmaniasis is still endemic.

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