Suppr超能文献

具有癌诊断陷阱的间变性淋巴瘤激酶阳性大B细胞淋巴瘤:一例报告

Anaplastic lymphoma kinase-positive large B-cell lymphoma with a diagnostic pitfall of carcinoma: a case report.

作者信息

Wei Ping, Jin Mulan, Jiang Lei, Wang Ying, Xie Jianlan, Hu Xiumei

机构信息

Department of Pathology, Beijing Friendship Hospital, Capital Medical University Beijing, China.

Department of Pathology, Beijing Chaoyang Hospital, Capital Medical University Beijing, China.

出版信息

Int J Clin Exp Pathol. 2017 Nov 1;10(11):11219-11224. eCollection 2017.

Abstract

Anaplastic lymphoma kinase-positive large B-cell lymphoma (ALK+LBCL) is a rare non-Hodgkin lymphoma that exhibits a characteristic immunoblastic/plasmablastic morphology and is frequently expressing Clathrin-anaplastic lymphoma kinase fusion protein. Since being negative for T- and B- linage markers, this tumor is easy to be misdiagnosed, especially when it has unusual morphology and immunophenotype. Here, we report an ALK+LBCL with a diagnostic pitfall of carcinoma. The patient was a 28-year-old man with enlargement of a right submandibular lymph node. Morphologically, the lymph node had an unusual nodular growth pattern, with nodules surrounded by collagen bands. The neoplastic cells expressed epithelial membrane antigen, CD138, CD38, Mum-1, but negative for T- and B- linage markers, and showed a strong granular cytoplasmic Anaplastic Lymphoma Kinase staining pattern. Some tumor cells had the expressing of Cytokeratin.

摘要

间变性淋巴瘤激酶阳性大B细胞淋巴瘤(ALK+LBCL)是一种罕见的非霍奇金淋巴瘤,具有特征性的免疫母细胞/浆母细胞形态,且常表达网格蛋白-间变性淋巴瘤激酶融合蛋白。由于该肿瘤T和B淋巴细胞标志物呈阴性,容易被误诊,尤其是当其具有不寻常的形态和免疫表型时。在此,我们报告一例ALK+LBCL误诊为癌的病例。患者为一名28岁男性,右颌下淋巴结肿大。形态学上淋巴结具有不寻常的结节状生长模式,结节被胶原带环绕。肿瘤细胞表达上皮膜抗原、CD138、CD38、Mum-1,但T和B淋巴细胞标志物呈阴性,并显示出强烈的颗粒状胞质间变性淋巴瘤激酶染色模式。一些肿瘤细胞表达细胞角蛋白。

相似文献

本文引用的文献

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验