Knowles D M
Semin Diagn Pathol. 1985 Aug;2(3):147-51.
Lymphoid infiltrates that originate outside of the major lymphoid tissue-bearing sites have often represented a difficult diagnostic problem, and the histopathologic criteria employed to distinguish between benign and malignant extranodal lymphoid infiltrates have not always resulted in accurate prognostication. In part, this has been due to the failure to recognize the existence of primary, extranodal, well-differentiated, small lymphocytic (WDL) lymphoma unassociated with systemic lymphoma or chronic lymphocytic leukemia, the presence of pseudofollicular proliferation centers within WDL lymphoma, and the existence of intermediate differentiated and mantle zone lymphomas that contain residual, atrophic, benign-appearing germinal centers. More recently, the determination of the mono- or polyclonality of extranodal lymphoid infiltrates has given us a new perspective on these lesions. Revisions of the histopathologic criteria and advances in immunology have increased our comprehension of the lymphoid proliferations that originate in the ocular adnexa, skin, lung, and gastrointestinal tract.
起源于主要淋巴组织承载部位之外的淋巴浸润常常是一个诊断难题,用于区分良性和恶性结外淋巴浸润的组织病理学标准并不总能得出准确的预后判断。部分原因在于未能认识到存在与系统性淋巴瘤或慢性淋巴细胞白血病无关的原发性、结外、高分化、小淋巴细胞(WDL)淋巴瘤,WDL淋巴瘤内假滤泡增殖中心的存在,以及存在含有残留、萎缩、外观良性生发中心的中间分化型和套区淋巴瘤。最近,结外淋巴浸润单克隆性或多克隆性的确定为我们对这些病变的认识提供了新视角。组织病理学标准的修订和免疫学的进展增强了我们对起源于眼附属器、皮肤、肺和胃肠道的淋巴增殖的理解。