Al-Maghrabi Haneen, Al-Maghrabi Jaudah
Department of Pathology and Laboratory Medicine, King Faisal Specialist Hospital and Research Center Jeddah, Saudi Arabia.
Department of Pathology, Faculty of Medicine, King Abdulaziz University Jeddah, Saudi Arabia.
Am J Clin Exp Urol. 2024 Oct 15;12(5):288-295. doi: 10.62347/GFNJ2400. eCollection 2024.
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.
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.
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.
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.
尿路和男性生殖器官淋巴瘤并不常见,占所有原发性结外淋巴瘤的比例不到5%。仅有少数小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。本研究的目的是调查在两家主要医院诊断为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年间诊断为原发性GU淋巴瘤的病例。检索并复查病理和免疫组织化学切片,对选定病例进行额外的免疫组织化学标记。
在此我们报告一项对11例患者的研究。诊断时的平均年龄为46岁(范围24 - 71岁)。在膀胱和输尿管淋巴瘤中,女性略占优势(3:2)。我们研究中观察到的病理淋巴瘤亚型为弥漫性大B细胞淋巴瘤(DLBCL)(36%);黏膜相关淋巴组织(MALT)淋巴瘤(18%);急性淋巴细胞白血病(B-LBL)(9%);高级别B细胞淋巴瘤(27%),其中1例具有伯基特样大细胞型组织形态学特征,以及1例高级别淋巴瘤,无法分类(9%)。在初次就诊时,患者通常表现为非特异性体征和症状。
尽管本研究再次证实了DLBCL在GU系统中的患病率,但也揭示了这些部位可能出现的淋巴瘤的多种类型。多种亚型凸显了通过免疫组织化学等辅助研究以及必要时的其他分子/细胞遗传学检测来全面表征淋巴瘤分类的重要性,因为它们对于实现准确的病理诊断至关重要。