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ALK 阴性间变大细胞淋巴瘤,具有“霍奇金样”细胞形态学特征和 PAX5 的核表达。

ALK-negative anaplastic large cell lymphoma with "Hodgkin-like" cytomorphology and nuclear expression of PAX5.

机构信息

Department of Surgical-Pathology/Hematopathology, Saint'Eugenio Hospital, Rome, Italy.

Hematology Unit, Saint' Eugenio Hospital, Rome, Italy.

出版信息

Pathol Res Pract. 2020 Feb;216(2):152724. doi: 10.1016/j.prp.2019.152724. Epub 2019 Oct 31.

DOI:10.1016/j.prp.2019.152724
PMID:31784094
Abstract

Anaplastic lymphoma kinase negative systemic anaplastic large cell lymphoma (ALK-ALCL) is a CD30+ T-cell malignant lymphoma which may involve both lymph nodes and extranodal tissues, showing important clinical differences from ALK-positive ALCL (ALK + ALCL). ALK- ALCL is considered a specific entity by the 2016 World Health Organization (WHO) classification of hematolymphoid neoplasms.We describe an exceptional case of ALK- ALCL with a striking "Hodgkin-like" cytomorphology and a very uncommon nuclear expression of PAX5.

摘要

间变性大细胞淋巴瘤,ALK 阴性(ALK-ALCL)是一种 CD30+ T 细胞恶性淋巴瘤,可累及淋巴结和结外组织,与间变性大细胞淋巴瘤,ALK 阳性(ALK+ALCL)相比具有重要的临床差异。ALK-ALCL 在 2016 年世界卫生组织(WHO)血液淋巴肿瘤分类中被认为是一种特殊实体。我们描述了一例罕见的 ALK-ALCL 病例,其具有显著的“霍奇金样”细胞形态学特征和非常罕见的 PAX5 核表达。

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