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IgA多发性骨髓瘤合并非典型成人T细胞白血病。

IgA multiple myeloma coexistent with atypical adult T-cell leukemia.

作者信息

Tagawa S, Okamoto Y, Inada E, Hakura A, Kitani T

机构信息

Division of Internal Medicine, Osaka University, Japan.

出版信息

Eur J Haematol. 1987 May;38(5):410-4. doi: 10.1111/j.1600-0609.1987.tb01437.x.

Abstract

We report a 65-yr-old male with adult T-cell leukemia (ATL) who developed multiple myeloma (MM) concomitantly. Skin lesions and peripheral leukocytosis were noted during the 5-yr observation period. There was abnormal lymphocytosis with indented or lobulated nuclei in the peripheral blood and in the bone marrow. The neoplastic cells reacted with monoclonal antibodies, OKT3, OKT4, OKIa1 and anti-Tac. His serum was positive for the antibodies to ATL-associated antigens. Human T-cell leukemia virus (HTLV) proviral DNA was detected in the leukemic cells. Thus, a diagnosis of ATL was made. There was IgA (k) paraprotein in his serum, and Bence-Jones protein (k) in urine samples. Fine needle aspiration revealed pathologic flaming plasma cells. Multiple osteolytic lesions appeared on his skull 5 yr after the initial examination. Thus, a diagnosis of MM concomitant with ATL was made.

摘要

我们报告一名65岁成年男性,患有成人T细胞白血病(ATL),并同时发生了多发性骨髓瘤(MM)。在5年的观察期内发现有皮肤病变和外周血白细胞增多。外周血和骨髓中存在核有凹陷或分叶的异常淋巴细胞增多。肿瘤细胞与单克隆抗体OKT3、OKT4、OKIa1和抗Tac发生反应。他的血清中ATL相关抗原抗体呈阳性。在白血病细胞中检测到人类T细胞白血病病毒(HTLV)前病毒DNA。因此,诊断为ATL。他的血清中有IgA(κ)副蛋白,尿样中有本-周蛋白(κ)。细针穿刺显示病理性火焰状浆细胞。初次检查5年后,他的颅骨上出现多个溶骨性病变。因此,诊断为MM合并ATL。

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