Kojima Masaru, Nakamura Naoya, Itoh Hideaki, Motoori Tadashi, Hoshi Kazue, Enomoto Yasunari, Johshita Takashi, Nakamine Hirokazu
Department of Anatomic and Diagnostic Pathology, Dokkyo University School of Medicine.
J Clin Exp Hematop. 2009 May;49(1):15-21. doi: 10.3960/jslrt.49.15.
Previous reports emphasized that localized lymphoid hyperplasia (LLH) of the large intestine is usually histologically characterized by large lymphoid follicles with striking enlarged germinal centers, and a narrow surrounding mantle zone and marginal zone (MZ). To clarify the histological varieties of LLH of the large intestine, 16 such cases have been studied. The present study demonstrated histological diversity of the LLH of the large intestine including (i) reactive follicular hyperplasia (RFH) (n=8), (ii) RFH with progressive transformation of the germinal center (PTGC) (n=3), (iii) RFH with MZ hyperplasia (n=3) and (iv) RFH with PTGC and MZ hyperplasia (n=2). Overall histomorphological findings of the present series appear quite different from previous descriptions of LLH of the large intestine. The present study showed histological variety of the LLH of the large intestine. Moreover, LLH of the large intestine should be differentiated from extranodal marginal zone B-cell lymphoma and nodular lymphocyte predominant Hodgkin lymphoma as well as follicular lymphoma. Immunohistological studies demonstrated the reactive nature of all 16 lesions. However, three cases showing RFH demonstrated immunoglobulin heavy chain gene rearrangement by polymerase chain reaction study in 12 cases examined. It remains unclear whether these three cases showing RFH could be a sign of the prelymphomatous stage (incipient follicular lymphoma) or representing merely an exaggeration of normal B-cell clonal response in the germinal centers.
既往报道强调,大肠局限性淋巴组织增生(LLH)在组织学上通常表现为大的淋巴滤泡,生发中心显著增大,周围有狭窄的套区和边缘区(MZ)。为阐明大肠LLH的组织学类型,对16例此类病例进行了研究。本研究显示大肠LLH具有组织学多样性,包括:(i)反应性滤泡增生(RFH)(n = 8),(ii)伴有生发中心进行性转化(PTGC)的RFH(n = 3),(iii)伴有MZ增生的RFH(n = 3),以及(iv)伴有PTGC和MZ增生的RFH(n = 2)。本系列病例的总体组织形态学表现与既往对大肠LLH的描述有很大不同。本研究显示了大肠LLH的组织学多样性。此外,大肠LLH应与结外边缘区B细胞淋巴瘤、结节性淋巴细胞为主型霍奇金淋巴瘤以及滤泡性淋巴瘤相鉴别。免疫组织学研究显示所有16个病变均具有反应性。然而,在12例接受检测的病例中,3例表现为RFH的病例经聚合酶链反应研究显示免疫球蛋白重链基因重排。目前尚不清楚这3例表现为RFH的病例是淋巴瘤前期(早期滤泡性淋巴瘤)的迹象,还是仅仅代表生发中心正常B细胞克隆反应的过度增强。