Clear Cell Carcinomas of Müllerian Type and Rete Testis Origin Presenting as Scrotal Masses: A Study of Seven Cases.

IF 4.5 1区 医学 Q1 PATHOLOGY American Journal of Surgical Pathology Pub Date : 2024-07-11 DOI:10.1097/PAS.0000000000002287
Irem Kilic, Andrés M Acosta, Thomas M Ulbright
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Abstract

Ovarian-type epithelial tumors involving the testis and paratestis are rare, with clear cell carcinomas (CCC) one of the least frequent. We report our experience with 4 müllerian-type (MT) CCCs presenting as testicular/scrotal masses and arising in the paratestis (n=2) and seminal vesicle (n=2; well supported in 1 case and likely in the other). In addition, we document 3 cases of papillary CCC exclusively within the rete testis (RTCCC) and seminiferous tubules and differing from the MT tumors. The patients with MTCCC were 24 to 85 years old (median, 42 y), and 2 had metastases at presentation. The 2 originating in the paratestis were associated with other MT tumors, an endometrioid borderline tumor and a papillary serous borderline tumor. The other 2 MTCCCs likely involved the testis via extension from seminal vesicle primaries through the vasa deferentia. All MTCCCs showed typical features, including tubules, simple papillae with hyalinized cores, and solid nests of polygonal clear cells with occasional hobnail features. Both paratesticular primaries showed sarcomatoid foci with tumor-associated neutrophilic infiltrates. The 3 RTCCCs presented in 54-, 57-, and 60-year-old men as testicular masses; they showed intrarete arborizing papillary growth with nonhyalinized fibrous cores and piled-up, solid foci, lacked hobnail cells, and expressed carbonic anhydrase IX (2/2) and CD10 (2/2) but not CA125, unlike the MTCCCs. On follow-up, 2 patients with MTCCC died of metastatic tumor (4 and 13.5 mo), a third developed ileal and retroperitoneal metastases at 13 months; and the fourth died at 13.5 months of unspecified cause. Follow-up of 2 patients with RTCCCs showed 1 disease free at 8 months and another alive with unknown disease status at 13 years. We conclude that CCCs involving the testis may either be of MT with often aggressive courses or show some features of renal tumors, with confinement to the rete testis and indolent behavior.

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表现为阴囊肿块的缪勒氏型和网状睾丸来源透明细胞癌:七例研究
累及睾丸和睾丸旁的卵巢型上皮肿瘤非常罕见,其中透明细胞癌(CCC)是最不常见的一种。我们报告了 4 例以睾丸/阴囊肿块为表现的穆勒氏型(MT)CCC,它们分别发生在睾丸旁(2 例)和精囊(2 例;其中 1 例证据确凿,另 1 例很可能)。此外,我们还记录了 3 例乳头状 CCC,这些肿瘤完全位于睾丸前叶(RTCCC)和曲细精管内,与 MT 型肿瘤不同。MTCCC患者的年龄从24岁到85岁不等(中位数为42岁),其中2例在发病时已有转移。2例起源于睾丸旁的肿瘤与其他MT肿瘤、子宫内膜样边界瘤和乳头状浆液性边界瘤有关。另外两例MTCCC很可能是从精囊原发肿瘤通过输精管延伸至睾丸。所有 MTCCC 均表现出典型特征,包括小管、带透明核心的单纯乳头状瘤、多角形透明细胞实性巢,偶尔伴有梭形细胞特征。两个睾丸旁原发灶均显示肉瘤样病灶,并伴有肿瘤相关的中性粒细胞浸润。3例 RTCCCs 患者分别为 54 岁、57 岁和 60 岁的男性,表现为睾丸肿块;它们表现为睾丸内轴化乳头状生长,伴有非钙化纤维核心和堆积的实性病灶,缺乏梭形细胞,表达碳酸酐酶 IX(2/2)和 CD10(2/2),但不表达 CA125,这与 MTCCCs 不同。随访期间,2 名 MTCCC 患者死于转移性肿瘤(4 个月和 13.5 个月),第 3 名患者在 13 个月时出现回肠和腹膜后转移,第 4 名患者在 13.5 个月时死于不明原因。对 2 名 RTCCCs 患者的随访结果显示,其中 1 人 8 个月后无病,另 1 人存活 13 年,但病情不明。我们的结论是,累及睾丸的CCC既可能是MT,病程通常具有侵袭性,也可能表现出肾肿瘤的某些特征,局限于睾丸隐窝且行为懒散。
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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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