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CD30阳性/ALK阴性高级别T细胞淋巴瘤与浆细胞骨髓瘤同时发生:一例报告

Simultaneous occurrence of a CD30 positive/ALK-negative high grade T-cell lymphoma and plasma cell myeloma: Report of a case.

作者信息

Nassif Samer, El-Majzoub Nadim, Abbas Ossama, Temraz Sally, Chakhachiro Zaher

机构信息

Department of Pathology and Laboratory Medicine, American University of Beirut Medical Center, Beirut, Lebanon.

Department of Pathology and Laboratory Medicine, American University of Beirut Medical Center, Beirut, Lebanon.

出版信息

Hematol Oncol Stem Cell Ther. 2015 Mar;8(1):40-2. doi: 10.1016/j.hemonc.2014.11.004. Epub 2014 Nov 27.

DOI:10.1016/j.hemonc.2014.11.004
PMID:25497976
Abstract

Simultaneous occurrences of T-cell and B-cell neoplasms are rare, and etiological relationships between these two malignancies are poorly understood. We report the case of a 76-year-old man who presented with hypercalcemia, multiple skin nodular lesions, fatigue, episodic fever, and night sweats. PET/CT scan showed diffuse skin and subcutaneous fat plane active lesions, supra- and infra- diaphragmatic active lymph nodes, liver and spleen involvement, bone marrow infiltration, and nonspecific bilateral lung nodules. A skin biopsy showed a high grade CD30-positive/ALK-negative T-cell lymphoma. A bone marrow biopsy showed involvement by the same neoplastic cells. Additionally, a monoclonal lambda restricted plasma cell population (15% of marrow elements) was identified, which, in view of an IgA lambda spike in the serum, was consistent with plasma cell myeloma. To the best of our knowledge, this case is the first reported case of a plasma cell neoplasm associated with an aggressive CD30-positive ALK-negative systemic T-cell lymphoma with skin involvement. Reporting such cases is important as it adds to the pool of rare cases of concomitant T-cell neoplasms and plasma cell myelomas, and might help in determining an etiological relationship, if any, between these two hematological malignancies.

摘要

T细胞和B细胞肿瘤同时发生的情况很少见,这两种恶性肿瘤之间的病因关系也知之甚少。我们报告了一例76岁男性患者,其表现为高钙血症、多发皮肤结节性病变、乏力、间歇性发热和盗汗。PET/CT扫描显示皮肤和皮下脂肪平面弥漫性活动性病变、膈上和膈下活动性淋巴结、肝脏和脾脏受累、骨髓浸润以及非特异性双侧肺结节。皮肤活检显示为高级别CD30阳性/ALK阴性T细胞淋巴瘤。骨髓活检显示相同的肿瘤细胞浸润。此外,还发现了单克隆λ限制性浆细胞群(占骨髓成分的15%),鉴于血清中存在IgAλ峰,这与浆细胞骨髓瘤一致。据我们所知,该病例是首例报告的与侵袭性CD30阳性ALK阴性系统性T细胞淋巴瘤伴皮肤受累相关的浆细胞肿瘤。报告此类病例很重要,因为它增加了T细胞肿瘤和浆细胞骨髓瘤同时发生的罕见病例库,并且可能有助于确定这两种血液系统恶性肿瘤之间是否存在病因关系。

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引用本文的文献

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Case Rep Hematol. 2020 Jan 16;2020:6309736. doi: 10.1155/2020/6309736. eCollection 2020.