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[儿童急性髓细胞白血病之前的明显骨髓坏死]

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

作者信息

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

机构信息

Department of Pediatrics, Shinshu University School of Medicine.

出版信息

Rinsho Ketsueki. 1991 Sep;32(9):991-5.

PMID:1942546
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.

摘要

1989年10月16日,一名3岁男孩因发热、腹痛和严重的全身性骨痛被转至我院。血液学检查显示血红蛋白8.7g/dl,白细胞计数5300/微升,中性粒细胞占9%,血小板计数5.5×10⁴/微升。骨髓穿刺和活检显示细胞明显坏死。血液生化检查显示CRP、血清LDH、FDP、FDP-D二聚体和纤维蛋白原短暂升高。Tc99m焦磷酸盐骨扫描显示不同骨骼有多个摄取点。尽管发热、腹痛和骨痛的症状在三周后自行消失,但贫血仍持续存在。骨髓坏死约两个月后,骨髓中出现异常细胞。诊断为急性髓系白血病(M3型)并开始联合化疗。该病例因急性期蛋白升高与骨髓坏死相关而引人注目。

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