Literature DB >> 1942546

[Marked bone marrow necrosis preceding acute myeloblastic leukemia in childhood].

H Sugiyama1, T Nakahata, T Kubo, T Kikuchi, Y Amano, N Okumura, A Komiyama.   

Abstract

A 3-year-old boy was transferred to our hospital because of fever, abdominal pain and severe systemic bone pain on October 16, 1989. Hematological examination showed hemoglobin 8.7 g/dl, white blood cell count 5300/microliters with 9% neutrophils and platelet count 5.5 x 10(4)/microliters. Bone marrow aspiration and biopsy revealed markedly necrotic cells. Blood chemistry showed transient elevation of CRP, serum LDH, FDP, FDP-Ddimer and fibrinogen. Tc99m pyrophosphate bone scanning showed multiple uptake spots in various bone. Although the sign of fever, abdominal pain and bone pain disappeared spontaneously after three weeks, anemia persisted. About two months later from bone marrow necrosis, abnormal cells appeared in the bone marrow. A diagnosis of AML (M3) was made and a combination chemotherapy started. This case is remarkable for elevation of acute phase protein in association with bone marrow necrosis.

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Year:  1991        PMID: 1942546

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


  1 in total

1.  Bone marrow necrosis in acute leukemia: Clinical characteristic and outcome.

Authors:  Talha Badar; Aditya Shetty; Carlos Bueso-Ramos; Jorge Cortes; Marina Konopleva; Gautam Borthakur; Sherry Pierce; Xuelin Huang; Hsiang-Chun Chen; Tapan Kadia; Naval Daver; Courtney Dinardo; Susan O'Brien; Guillermo Garcia-Manero; Hagop Kantarjian; Farhad Ravandi
Journal:  Am J Hematol       Date:  2015-07-27       Impact factor: 10.047

  1 in total

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