| Literature DB >> 11844970 |
Ryusuke Mizukane1, Jun-ichi Kadota Ji, Toshiyuki Yamaguchi, Takakazu Kiya, Hiromichi Fukushima, Masao Nakatomi, Shigeru Kohno.
Abstract
We present an extremely rare case of hemophagocytic syndrome (HPS) induced by fulminant Mycoplasma pneumoniae (Mp) pneumonia in an elderly adult. Erythrocytopenia and thrombocytopenia were observed in a patient with acute respiratory failure, liver dysfunction and renal failure. Mp-associated HPS was diagnosed in this case by clinical and laboratory findings, including a bone marrow aspiration specimen and serum Mp antibody titer. High serum levels of soluble interleukin-2 receptor, interleukin-6, human interleukin-10 and macrophage-colony stimulating factor were observed. Hypercytokinemia is a useful marker of disease activity and prognosis. Combined treatment with methylprednisolone and erythromycin was successful and led to a favorable outcome. Physicians should be aware of HPS as a complication in Mp infection. Copyright 2002 S. Karger AG, BaselEntities:
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Year: 2002 PMID: 11844970 DOI: 10.1159/000049377
Source DB: PubMed Journal: Respiration ISSN: 0025-7931 Impact factor: 3.580