Oishi Naoki, Montes-Moreno Santiago, Feldman Andrew L
Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN 55905, USA; Department of Pathology, University of Yamanashi, Chuo, Yamanashi 409-3898, Japan.
Pathology Service and Translational Hematopathology Lab, Hospital Universitario Marques de Valdecilla/IDIVAL, Santander, Spain.
Semin Diagn Pathol. 2018 Jan;35(1):76-83. doi: 10.1053/j.semdp.2017.11.001. Epub 2017 Nov 10.
In situ neoplasia represents the earliest form of malignant progression and is characterized by localization limited to the compartment corresponding to the cell of origin. Like other cancers, lymphoid neoplasms are considered to develop by multistep pathogenetic mechanisms. However, because of the circulating nature of lymphocytes, in situ lymphoid neoplasia may be difficult to identify histopathologically, and the compartment to which it is restricted may be physiological rather than strictly anatomical. The 2016 WHO classification of lymphoid neoplasms recognizes two in situ entities: in situ follicular neoplasia (ISFN) and in situ mantle cell neoplasia (ISMCN). This review summarizes the clinical features, histopathology, genetics, and differential diagnoses of these two entities, including distinction from both their overly malignant counterparts and a variety of reactive processes.
原位肿瘤形成代表恶性进展的最早形式,其特征是局限于与起源细胞相对应的区域。与其他癌症一样,淋巴样肿瘤被认为是通过多步骤致病机制发展而来。然而,由于淋巴细胞的循环特性,原位淋巴样肿瘤可能难以通过组织病理学识别,并且其受限的区域可能是生理性的而非严格解剖学上的。2016年世界卫生组织淋巴样肿瘤分类认可两种原位病变:原位滤泡性肿瘤(ISFN)和原位套细胞肿瘤(ISMCN)。本综述总结了这两种病变的临床特征、组织病理学、遗传学及鉴别诊断,包括与它们的过度恶性对应物以及各种反应性过程的区分。