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[弥漫性大B细胞淋巴瘤在抗CD20单克隆抗体(利妥昔单抗)治疗后立即复发为CD20阴性的多发性皮肤肿瘤]

[Relapse of diffuse large B cell lymphoma to CD20-negative multiple cutaneous tumors immediately after anti-CD20 monoclonal antibody (rituximab) therapy].

作者信息

Iguchi Tomotaka, Miyazawa Keisuke, Okabe Seiichi, Kawakubo Ken, Shimamoto Takashi, Kuriyama Yuzuru, Ito Yoshikazu, Kimura Yukihiko, Ohyashiki Kazuma, Serizawa Hiromi, Iwaya Keiici, Mukai Kiyoshi

机构信息

First Department of Internal Medicine, Tokyo Medical University.

出版信息

Rinsho Ketsueki. 2004 Oct;45(10):1129-34.

Abstract

A 60-year-old male was referred to our hospital because of cervical lymphadenopathy and a left hilar abnormal shadow seen on chest X-ray in May 1999. The pathological findings of the cervical lymph nodes revealed that the patient had a malignant lymphoma, of the diffuse large B cell type, at clinical stage IIIB. Immunohistochemistry demonstrated that the lymphoma cells were positive for CD11a, CD19, CD20, CD23, CD25, CD45, IgM, IgD and lambda, but negative for CD5. Although a complete remission was obtained after 8 courses of CHOP therapy, the patient relapsed 32 months later. Two courses of a half dose of CHASE therapy consisting of CPM, ara-C, VP-16 and dexamethasone, followed by rituximab (600 mg/week x4) resulted in a transient re-induction of complete remission. However, multiple cutaneous tumors became apparent just 10 days after the last rituximab therapy. Immunohistochemistry of the cutaneous tumors revealed infiltration of CD20-negative lymphoma cells. A series of chemotherapy including high-dose MTX was ineffective, and the patient died in August 2003. Autopsy findings revealed the systemic intra-capillary infiltration of CD20 negative-lymphoma cells into multiple organs, including the lungs, liver, and kidneys. A CD20 negative-clone selected by rituximab therapy appeared to have expanded in this case.

摘要

一名60岁男性因颈部淋巴结病及1999年5月胸部X线检查发现左肺门异常阴影而转诊至我院。颈部淋巴结的病理检查结果显示,该患者患有弥漫性大B细胞型恶性淋巴瘤,临床分期为IIIB期。免疫组织化学显示淋巴瘤细胞CD11a、CD19、CD20、CD23、CD25、CD45、IgM、IgD及λ呈阳性,但CD5呈阴性。尽管经过8个疗程的CHOP治疗后达到完全缓解,但患者在32个月后复发。采用由环磷酰胺、阿糖胞苷、依托泊苷及地塞米松组成的半量CHASE方案进行两个疗程治疗,随后给予利妥昔单抗(600mg/周×4),导致短暂再次诱导完全缓解。然而,在最后一次利妥昔单抗治疗仅10天后,多处皮肤肿瘤出现。皮肤肿瘤的免疫组织化学检查显示CD20阴性淋巴瘤细胞浸润。包括大剂量甲氨蝶呤在内的一系列化疗均无效,患者于2003年8月死亡。尸检结果显示,CD20阴性淋巴瘤细胞在全身毛细血管内浸润至包括肺、肝和肾在内的多个器官。在该病例中,经利妥昔单抗治疗选择的CD20阴性克隆似乎有所扩增。

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