累及泌尿生殖道的非霍奇金原发性淋巴瘤:沙特阿拉伯西部地区两家三级医院的组织病理学经验。

IF 1.5 Q3 UROLOGY & NEPHROLOGY
American journal of clinical and experimental urology Pub Date : 2024-10-15 eCollection Date: 2024-01-01 DOI:10.62347/GFNJ2400
Haneen Al-Maghrabi, Jaudah Al-Maghrabi
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引用次数: 0

摘要

背景:尿路和男性生殖器官淋巴肿瘤并不常见,在所有原发性结外淋巴瘤中占比不到 5%。目前只有少数小型病例系列和个别病例报告描述了这些肿瘤的原发部位和亚型。本研究旨在调查在两家大型医院确诊的原发性泌尿生殖系统(GU)淋巴瘤患者的病理特征:我们收集了2005年至2020年间被诊断为原发性泌尿生殖系统淋巴瘤的病例。我们检索并审查了病理切片和免疫组化切片,并对部分病例做了额外的免疫组化标记:结果:我们在此对 11 例患者进行了研究。诊断时的平均年龄为 46 岁(24-71 岁)。在膀胱和输尿管淋巴瘤中,女性略占多数(3:2)。我们的研究观察到的病理淋巴瘤亚型包括弥漫大 B 细胞淋巴瘤(DLBCL)(36%);粘膜相关淋巴组织淋巴瘤(MALT)(18%);急性淋巴细胞淋巴瘤(B-LBL)(9%);高级别 B 细胞淋巴瘤(27%),其中一例组织形态学为伯基特样大细胞型,还有一例高级别淋巴瘤,无法分类(9%)。在发病初期,患者通常伴有非特异性症状和体征:这项研究再次证实了 DLBCL 在上咽部系统的发病率,同时也揭示了这些部位可能出现的各种淋巴瘤。亚型的多样性凸显了通过辅助研究(如免疫组化和其他必要的分子/细胞遗传学检测)对淋巴瘤分类进行彻底定性的重要性,因为它们对于获得准确的病理诊断至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Non-Hodgkin's primary lymphoma involving the genitourinary tract: histopathological experience from two tertiary hospitals, Western region, Saudi Arabia.

Background: Urinary tract and male genital organ lymphoid neoplasms are uncommon, accounting for less than 5% of all primary extranodal lymphomas. There have only been a few small case series and isolated case reports describing the primary sites and subtypes of these neoplasms. The aim of the study is to investigate the pathological characteristics of patients diagnosed with primary Genitourinary (GU) lymphoma in at two major hospitals.

Material and methods: We obtained cases that were diagnosed with primary GU lymphomas between 2005 and 2020. Pathology and immunohistochemistry slides were retrieved and reviewed, additional immunohistochemical markers were done on selected cases.

Result: Herein we present a study of 11 patients. The mean age at diagnosis time was 46 years (range 24-71 years). Among urinary bladder, and ureter lymphomas, a slight female predominance was noted (3:2). Pathologic lymphoma subtype observed in our study were diffuse large B-cell lymphoma (DLBCL) (36%); mucosa-associated lymphoid tissue (MALT) lymphoma (18%); acute lymphoblastic lymphoma (B-LBL) (9%); high-grade B-cell lymphomas (27%) one of them with histomorphology of Burkitt-like large cell type, and a case of high-grade lymphoma, unclassifiable (9%). At the initial time of presentation, patients were commonly presented with non-specific signs and symptoms.

Conclusion: Even though this study reaffirms the prevalence of DLBCL in GU system, it also sheds light on the variable range of lymphomas that can arise in these sites. The variety of subtypes highlights the significance of thoroughly characterizing lymphoma classifications through ancillary studies such as immunohistochemistry and other molecular/cytogenetic tests if needed, as they are crucial for achieving an accurate pathology diagnosis.

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