可能起源于沃尔夫的女性附件肿瘤(沃尔夫瘤):腹膜间皮瘤的潜在模拟物

IF 4.5 1区 医学 Q1 PATHOLOGY
American Journal of Surgical Pathology Pub Date : 2024-08-01 Epub Date: 2024-06-25 DOI:10.1097/PAS.0000000000002237
Kianoosh Keyhanian, Tanner Mack, Erna Forgo, Henry Tazelaar, Teri A Longacre
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引用次数: 0

摘要

沃尔夫瘤(Wolffian tumor)及其最近定义的 STK11 附件肿瘤(STK11 adnexal tumor)是一种罕见的肿瘤,被认为是由肾间质残余物引起的。这些肿瘤通常发生在阔韧带、输卵管和卵巢轴,虽然大多数预后良好,但高达 50% 的 STK11 附件肿瘤表现出侵袭性临床表现。主要的鉴别诊断包括子宫内膜样腺癌和性索间质瘤。然而,这些肿瘤的形态学和免疫组化特征与腹膜间皮瘤有相当多的重叠。为了全面描述这些肿瘤的免疫表型特征,我们使用用于诊断间皮瘤的标准标记物对 21 个病例(18 个沃尔夫肿瘤和 3 个 STK11 附件肿瘤)进行了检查。我们对病例的形态学和免疫组化(IHC)特征进行了审查,并对有可用材料的病例进行了额外的 IHC 检测。患者年龄从 25 岁到 73 岁(平均 51 岁)不等。肿瘤部位包括附件/阔韧带(6 例,28%)、输卵管旁(5 例,24%)、卵巢/卵巢旁(5 例,24%)、输卵管(腔内)(2 例,9.5%)、盆腔(2 例,9.5%)和肝脏(1 例,5%)。肿瘤平均大小为 9.3 厘米(范围:0.2 至 22 厘米)。大多数病例(14/21,66%)的组织形态为管状至实性片状肿瘤细胞,内衬为柱状至立方体细胞,含有均匀的圆形至椭圆形核。至少有 7 例(33%)病例中还可见具有缝隙状腔隙和筛状形态的压缩小管。有三个病例显示,上皮样细胞在突出的肌样基质中生长出具有楔形和微尖模式的网状索和小梁,这在 STK11 附件肿瘤中已有描述。在可对 3 种间皮细胞标记物(钙网素、WT1、D2-40)进行 IHC 检测的病例中,55.5%(9 例中的 5 例)对所有 3 种标记物均有反应。在至少有 2 种间皮细胞标记物的病例中,69%(11/16)的 2 种标记物(主要是钙网蛋白和 WT1)呈阳性。在大多数检测病例中,Claudin-4、MOC31 和 BER-EP4 均为阴性(分别为 78% [7/9]、71.4% [5/7] 和 100% [6/6])。鉴于与间皮瘤的相似性,有 3 个病例(14%)最初强烈考虑和/或实际误诊为间皮瘤。总之,沃尔夫瘤及其最近定义的亲属 STK11 附件肿瘤的形态学和免疫组化特征可导致间皮瘤的误诊,尤其是在发生播散或转移时。在所有盆腔和腹膜间皮瘤的鉴别诊断中都应考虑沃尔夫瘤和STK11附件肿瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Female Adnexal Tumor of Probable Wolffian Origin (Wolffian Tumor): A Potential Mimic of Peritoneal Mesothelioma.

Wolffian tumor and its nosologic relative, the recently defined STK11 adnexal tumor are rare neoplasms thought to arise from mesonephric remnants. These tumors typically arise in the broad ligament, fallopian tube, and ovarian hilum and although most are associated with a good prognosis, up to 50% of STK11 adnexal tumors demonstrate aggressive clinical behavior. The chief differential diagnoses include endometrioid adenocarcinoma and sex cord stromal tumors. However, the morphologic and immunohistochemical features of these tumors exhibit considerable overlap with peritoneal mesothelioma. To fully characterize their immunophenotypic signature, we examined a total of 21 cases (18 Wolffian and 3 STK11 adnexal tumors) with standard markers used in the diagnosis of mesothelioma. Morphologic and immunohistochemical (IHC) features were reviewed and additional IHC performed for cases with available material. Patient age ranged from 25 to 73 (mean: 51) years. Sites included adnexa/broad ligament (6, 28%), paratubal (5, 24%), ovary/paraovarian (5, 24%), tubal (intraluminal) (2, 9.5%), pelvis (2, 9.5%), and liver (1, 5%). The mean tumor size was 9.3 cm (range: 0.2 to 22 cm). The histomorphology in most cases (14/21, 66%) consisted of tubular to solid sheets of neoplastic cells lined by columnar to cuboidal cells containing uniform round to oval nuclei. Compressed tubules with slit-like lumens and sieve-like pattern were also seen in at least 7 (33%) cases. Three cases demonstrated interanastomosing cords and trabeculae of epithelioid cells with cribriform and microacinar patterns growing within prominent myxoid stroma as described in STK11 adnexal tumors. In the cases with available IHC for 3 mesothelial markers (calretinin, WT1, D2-40), 55.5% (5 of 9) showed reactivity with all 3 markers. In cases with at least 2 available mesothelial markers, 69% (11/16) were positive for 2 markers (mostly calretinin and WT1). Claudin-4, MOC31, and BER-EP4 were negative in most cases tested (78% [7/9], 71.4% [5/7], and 100% [6/6], respectively). Given the resemblance to mesothelioma, there was initial strong consideration and/or actual misdiagnosis of mesothelioma in 3 cases (14%). In summary, the morphologic and immunohistochemical features of Wolffian tumor and its recently defined relative, STK11 adnexal tumor, can lead to misdiagnosis of mesothelioma, particularly when encountered in the disseminated or metastatic setting. Wolffian tumor and STK11 adnexal tumor should be considered in the differential diagnosis of all pelvic and peritoneal mesotheliomas.

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来源期刊
CiteScore
10.30
自引率
5.40%
发文量
295
审稿时长
1 months
期刊介绍: The American Journal of Surgical Pathology has achieved worldwide recognition for its outstanding coverage of the state of the art in human surgical pathology. In each monthly issue, experts present original articles, review articles, detailed case reports, and special features, enhanced by superb illustrations. Coverage encompasses technical methods, diagnostic aids, and frozen-section diagnosis, in addition to detailed pathologic studies of a wide range of disease entities. Official Journal of The Arthur Purdy Stout Society of Surgical Pathologists and The Gastrointestinal Pathology Society.
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