Literature DB >> 8691575

[Reactive hemophagocytic syndrome responded to combination chemotherapy with steroid pulse therapy].

T Okuda1, Y Yumoto.   

Abstract

A 66-year-old male was admitted to our hospital because of persistent fever. Laboratory data revealed leukopenia, thrombocytopenia, marked elevation of serum lactic acid dehydrogenase and ferritin levels, as well as disseminated intravascular coagulophathy (DIC). Bone marrow aspiration showed increased numbers of mature histiocytes with hemophagocytosis and a diagnosis of reactive hemophagocytic syndrome was made. In the broad spectrum of this syndrome, we suspected virus-associated hemophagocytic syndrome (VAHS) but no causative viral infection was detected. Since DIC is known to be a poor prognostic factor, he was given combination chemotherapy containing VP-16 in addition to pulse therapy of methylprednisolone. He completely recovered after the treatment. Chemotherapy is one option in the treatment of adult onset reactive hemophagocytic syndrome.

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Year:  1995        PMID: 8691575

Source DB:  PubMed          Journal:  Rinsho Ketsueki        ISSN: 0485-1439


  2 in total

1.  A clinical study of 21 patients with hemophagocytic syndrome in 295 cases diagnosed with nasal type, extranodal nature killer/T cell lymphoma.

Authors:  Na Li; Li Zhang; Jie Liu; Jing Zhang; Hua-Wei Weng; Hong-Yu Zhuo; Li-Qun Zou
Journal:  Cancer Biol Ther       Date:  2017-02-25       Impact factor: 4.742

2.  Profile of hemophagocytic lymphohistiocytosis; efficacy of intravenous immunoglobulin therapy.

Authors:  Sarala Rajajee; Indhumathi Ashok; Nitin Manwani; J Rajkumar; Kalpana Gowrishankar; Ezhilarasi Subbiah
Journal:  Indian J Pediatr       Date:  2014-05-09       Impact factor: 5.319

  2 in total

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