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[伴有纵隔巨大肿块病变的CD7(+)急性髓系白血病(M0)]

[CD7(+) acute myeloid leukemia (M0) associated with a mediastinal bulky mass lesion].

作者信息

Yoshida K, Kusumoto S, Sugahara Y, Yagasaki F, Sakata T, Kawai N, Matsuda A, Suzuki T, Hirashima K, Kayano H, Bessho M

机构信息

First Department of Internal Medicine, Saitama Medical School.

出版信息

Rinsho Ketsueki. 2001 Aug;42(8):644-9.

PMID:11579505
Abstract

A 41-year-old man visited his doctor in May 2000 because of a sore throat and high fever. His symptoms did not improve, despite administration of antibiotics and nonsteroidal anti-inflammatory drugs. Since a chest X-ray examination revealed an anterior mediastinal bulky tumor, he was referred and admitted to our hospital on June 21, 2000. The peripheral white blood cell count was 44,540/microliter with 74% myeloblasts. Bone marrow aspiration revealed a hypercellular marrow with 82% myeloblasts, which were negative for peroxidase and alpha-naphthyl butylate esterase staining. Blast cells were positive for CD7, CD13, CD33, CD34, and HLA-DR, and negative for CD56. A needle biopsy specimen of the mediastinal tumor consisted of myeloblasts. We diagnosed the patient as having CD7 (+) acute myeloid leukemia (AML) (M0) with a bulky mediastinal mass based on the surface marker analysis, although the clinical features resembled myeloid/NK precursor acute leukemia. The patient achieved a complete remission after two courses of induction therapy. We are planning an allogeneic stem cell transplantation during his first remission because of the high risk of relapse.

摘要

一名41岁男性因喉咙痛和高烧于2000年5月就医。尽管使用了抗生素和非甾体抗炎药,他的症状仍未改善。由于胸部X光检查发现前纵隔有一个巨大肿瘤,他于2000年6月21日被转诊并入住我院。外周血白细胞计数为44,540/微升,其中原始粒细胞占74%。骨髓穿刺显示骨髓细胞增多,原始粒细胞占82%,过氧化物酶和α-萘丁酸酯酶染色均为阴性。原始细胞CD7、CD13、CD33、CD34和HLA-DR呈阳性,CD56呈阴性。纵隔肿瘤的针吸活检标本由原始粒细胞组成。根据表面标志物分析,我们诊断该患者患有CD7(+)急性髓系白血病(AML)(M0)伴巨大纵隔肿块,尽管其临床特征类似于髓系/NK前体急性白血病。该患者在两个疗程的诱导治疗后达到完全缓解。由于复发风险高,我们计划在他首次缓解期间进行异基因干细胞移植。

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Rinsho Ketsueki. 2001 Aug;42(8):644-9.
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Myeloid/NK cell precursor acute leukemia lost both CD13 and CD33 at first diagnosis.髓系/自然杀伤细胞前体急性白血病在初次诊断时同时丧失了CD13和CD33。
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