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急性髓系白血病M5b在Castleman病临床缓解期发生。

Acute myelogenous leukemia M5b developed during clinical remission of Castleman disease.

作者信息

Tomonari Akira, Shirafuji Naoki, Tojo Arinobu, Iseki Tohru, Ooi Jun, Komiya Itaru, Tani Kenzaburo, Asano Shigetaka

机构信息

Department of Hematology/Oncology, The Institute of Medical Science, The University of Tokyo, Japan.

出版信息

Int J Hematol. 2003 Apr;77(3):274-6. doi: 10.1007/BF02983785.

Abstract

Castleman disease (CD) is a rare heterogeneous lymphoproliferative disease characterized by clinical symptoms due to an excess of interleukin-6 (IL-6) or IL-6-like activity. We describe the first case of CD associated with acute myelogenous leukemia (AML). A 55-year-old man presented with skin rash on his face and multiple cervical lymphadenopathy. The results of examination of his lymph node biopsy specimen led to a diagnosis of CD. The symptoms resolved after the administration of prednisolone. Three years after the onset of CD, the patient's white blood cell count had increased to 63.4 x 10(9)/L. His bone marrow aspirate showed that approximately 80% of cells were leukemic, including well-differentiated monocytic cells A diagnosis of AML M5b was made. The patient died of invasive pulmonary aspergillosis after chemotherapy.

摘要

卡斯特曼病(CD)是一种罕见的异质性淋巴增生性疾病,其特征为因白细胞介素-6(IL-6)或IL-6样活性过高而出现临床症状。我们报告首例与急性髓系白血病(AML)相关的CD病例。一名55岁男性出现面部皮疹和多处颈部淋巴结病。其淋巴结活检标本的检查结果确诊为CD。给予泼尼松龙后症状缓解。CD发病三年后,患者白细胞计数增至63.4×10⁹/L。其骨髓穿刺显示约80%的细胞为白血病细胞,包括分化良好的单核细胞,诊断为AML M5b。该患者化疗后死于侵袭性肺曲霉病。

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