| Literature DB >> 27025597 |
Athanasios Tragiannidis1, Maria Papageorgiou2, Maria Stamou2, Emmanuel Hatzipantelis2, Theodotis Papageorgiou2, Andreas Giannopoulos2, Lamprini Damianidou2, Anna Pappa3, Stiliani Pappa3, Maria Hatzistilianou2.
Abstract
A 2.5-year-old girl was admitted due to splenomegaly and pancytopenia. Laboratory analysis revealed pancytopenia and hypergammaglobulinemia, and due to the absence of fever and the relevant clinical and hematological presentation the child was initially suspected for acute lymphoblastic leukemia. Bone marrow aspiration displayed macrophages and extracellular space containing Leishmania amastigotes. Visceral leishmaniasis diagnosis due to Leishmania infantum was confirmed by the presence of high titers of Leishmania antibodies and by PCR. The patient was successfully treated with liposomal amphotericin B but during the third post-treatment day significant increases in the levels of serum uric acid, blood urea nitrogen, and phosphate were registered. The child was successfully treated with hydration and urine alkalization and resulted in full recovery of the metabolic abnormalities.Entities:
Keywords: childhood; liposomal amphotericin B; lysis syndrome; visceral leishmaniasis
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Year: 2016 PMID: 27025597 PMCID: PMC5806763 DOI: 10.1177/0394632016640788
Source DB: PubMed Journal: Int J Immunopathol Pharmacol ISSN: 0394-6320 Impact factor: 3.219