Department of Pathology, Division of Women's and Perinatal Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA.
Department of Pathology, University of Michigan Hospital, Ann Arbor, MI.
Am J Surg Pathol. 2024 Aug 1;48(8):972-984. doi: 10.1097/PAS.0000000000002232. Epub 2024 May 2.
Ewing sarcoma is an uncommon neoplasm considered in the differential diagnosis of tumors with "small round cell" morphology, but its occurrence in the gynecologic tract has only been sporadically documented. Herein, we describe the largest cohort of Ewing sarcoma localized to the female genital tract to date, and emphasize their clinicopathologic resemblance to more common gynecologic neoplasms. Ewing sarcoma (n=21) was retrospectively identified from 5 institutions. The average patient age was 35 (range 6-61) years. Tumor sites included uterus (n=8), cervix (n=4), vulva (n=5), vagina (n=1), broad ligament (n=1), inguinal area (n=1), and pelvis (n=1). Nine of 18 cases in which slides were available for review demonstrated only classic round cell morphology, with the remainder showing a variable combination and prominence of variant ovoid/spindle or epithelioid appearance. Tumors showed diffuse membranous reactivity for CD99 (20/20) and were positive for NKX2.2 (8/8, diffuse) and cyclin D1 (7/7, of which 3/7 were patchy/multifocal and 4/7 were diffuse). They were negative for ER (0/6) and CD10 (0/6). Three cases were initially diagnosed as endometrial stromal sarcomas. EWSR1 rearrangement was confirmed in 20/21 by fluorescence in situ hybridization (n=15) and/or sequencing (n=8). Of the eight tumors that underwent sequencing, 6 harbored FLI1 , 1 ERG, and 1 FEV as the fusion partner. Of 11 patients with available follow-up, 5 died of disease, 1 developed lung metastases and 5 are alive with no evidence of disease. Ewing sarcoma of the gynecologic tract is a rare, aggressive entity that shares some morphologic and immunohistochemical features with other more common gynecologic neoplasms. In addition to the typical round cell appearance, variant spindled/ovoid to epithelioid morphology may also be observed and should prompt consideration of this entity with appropriate immunohistochemical and/or molecular studies.
尤文肉瘤是一种罕见的肿瘤,在“小圆细胞”形态的肿瘤鉴别诊断中需要考虑,但在妇科生殖道中的发生仅零星记录。在此,我们描述了迄今为止最大的一组定位于女性生殖道的尤文肉瘤队列,并强调了它们与更常见的妇科肿瘤在临床病理上的相似性。尤文肉瘤(n=21)从 5 个机构中回顾性地确定。平均患者年龄为 35 岁(范围 6-61 岁)。肿瘤部位包括子宫(n=8)、宫颈(n=4)、外阴(n=5)、阴道(n=1)、阔韧带(n=1)、腹股沟区(n=1)和骨盆(n=1)。在有切片可供审查的 18 例中有 9 例仅显示经典的小圆细胞形态,其余的则显示出各种形态和突出的卵圆形/梭形或上皮样外观的组合。肿瘤对 CD99(20/20)表现出弥漫性膜反应,并对 NKX2.2(8/8,弥漫性)和 cyclin D1(7/7,其中 3/7 为斑片状/多灶性,4/7 为弥漫性)呈阳性。它们对 ER(0/6)和 CD10(0/6)呈阴性。3 例最初诊断为子宫内膜间质肉瘤。通过荧光原位杂交(n=15)和/或测序(n=8)证实 20/21 例存在 EWSR1 重排。在进行测序的 8 个肿瘤中,6 个存在 FLI1、1 个存在 ERG 和 1 个存在 FEV 作为融合伴侣。在 11 例有随访资料的患者中,5 例死于疾病,1 例发生肺转移,5 例存活且无疾病证据。妇科生殖道的尤文肉瘤是一种罕见的侵袭性实体,在形态学和免疫组织化学特征上与其他更常见的妇科肿瘤有一些相似之处。除了典型的小圆细胞外观外,还可能观察到变体梭形/卵圆形至上皮样形态,应通过适当的免疫组织化学和/或分子研究提示考虑该实体。