Department of Anatomic Pathology, Kyushu University Graduate School of Medicine Sciences, 812-8582, Fukuoka, Japan.
Department of Anatomic Pathology, Kyushu University Graduate School of Medicine Sciences, 812-8582, Fukuoka, Japan.
Hum Pathol. 2022 Feb;120:88-98. doi: 10.1016/j.humpath.2021.12.010. Epub 2022 Jan 4.
Lymphoproliferative disorder (LPD) can occur in patients with inflammatory bowel disease (IBD) such as ulcerative colitis (UC) and Crohn's disease (CD). On rare occasions, patients with IBD develop myeloid neoplasms; however, the frequency and clinicopathological features of IBD-associated lymphoid and myeloid proliferative disorder (LMPD) in Japanese patients are still unclear. In this study, we reviewed 2474 Japanese patients with IBD and found that LMPD occurred in 12 (0.5%) patients with UC (n = 7) or CD (n = 5). Together with an additional 3 cases, we analyzed a total of 15 cases of LMPD for clinicopathological and histological features. Based on the status of using immunosuppressants such as biologics and immunomodulators, Epstein-Barr virus (EBV) infection, and histopathology, the 15 cases were classified into Group I (high-grade LPD; n = 7), Group II (low-grade LPD; n = 5), and Group III (myeloid neoplasms; n = 3). Most patients in Group I were undergoing strong immunosuppressive therapy, and the LPD lesions corresponded to high-grade B-cell or T cell/natural killer cell lymphoma often with EBV infection. Discontinuation of immunosuppressive drugs alone did not resolve these LPDs; Group I patients required chemotherapy, and eventually 4 of them (57%) died of the tumor. Most cases in Group II were low-grade B-cell lymphoma without EBV infection and had an indolent clinical course with excellent prognosis. All patients in Group III developed acute myeloid leukemia (AML) during the course of CD. Two (67%) of these patients died of AML. Our study suggests that IBD-associated LMPD is very rare but can follow an aggressive clinical course.
淋巴增殖性疾病(LPD)可发生于炎症性肠病(IBD)患者,如溃疡性结肠炎(UC)和克罗恩病(CD)。在极少数情况下,IBD 患者会发展为髓系肿瘤;然而,日本患者中 IBD 相关的淋巴和髓系增殖性疾病(LMPD)的频率和临床病理特征仍不清楚。在这项研究中,我们回顾了 2474 例日本 IBD 患者,发现 12 例(0.5%)UC(n=7)或 CD(n=5)患者发生 LMPD。加上另外 3 例,我们共分析了 15 例 LMPD 的临床病理和组织学特征。根据是否使用免疫抑制剂(如生物制剂和免疫调节剂)、EB 病毒(EBV)感染以及组织病理学情况,这 15 例被分为 I 组(高级别 LPD;n=7)、II 组(低级别 LPD;n=5)和 III 组(髓系肿瘤;n=3)。I 组的大多数患者正在接受强烈的免疫抑制治疗,LPD 病变对应于高级别 B 细胞或 T 细胞/自然杀伤细胞淋巴瘤,常伴有 EBV 感染。单独停用免疫抑制剂并不能解决这些 LPD;I 组患者需要化疗,最终其中 4 例(57%)死于肿瘤。II 组的大多数病例为无 EBV 感染的低级别 B 细胞淋巴瘤,具有惰性的临床病程和良好的预后。III 组的所有患者在 CD 病程中均发展为急性髓系白血病(AML)。其中 2 例(67%)患者死于 AML。我们的研究表明,IBD 相关的 LMPD 非常罕见,但可表现为侵袭性临床病程。