A 37-Year-Old Man with Multifocal Bilateral Malignant Testicular Large-Cell Calcifying Sertoli Cell Tumors Presenting as Painless Testicular Masses.

IF 0.7 Q3 MEDICINE, GENERAL & INTERNAL American Journal of Case Reports Pub Date : 2025-02-13 DOI:10.12659/AJCR.945910
Lukas Dohmen, Mélissa Pani, Pierre Marchettini, François Devos
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Abstract

BACKGROUND Large-cell calcifying Sertoli cell tumor (LCCSCT) belongs to the category of sex cord stromal tumors and is extremely rare. Testicular LCCSCTs show benign or malignant behavior, appear sporadically, or are associated with genetic syndromes. Benign LCCSCTs are more commonly bilateral and multifocal and present in younger patients. The prognosis is poor when patients have advanced or metastatic disease. However, due to its rarity, the literature provides only weak evidence concerning their clinical course and treatment options. This report describes a 37-year-old man suffering from a multifocal, bilateral malignant testicular LCCSCT presenting as painless testicular masses. CASE REPORT A 37-year-old man presented with bilateral painless testicular masses. Imagery showed bilateral macro-orchitis with multifocal intratesticular hyperechoic and hypointense lesions. He underwent testis-sparing surgery with the enucleation of 1 testicular lesion. The anatomopathological analysis revealed an LCCSCT whose histological characteristics indicated a benign tumor. A simple follow-up was therefore recommended. Six years after diagnosis, the patient developed lymph node metastases, and radical bilateral orchiectomy and radical lymphadenectomy were performed. A few months later, pleural, pulmonary, and bone metastases occurred. Chemotherapy and immunotherapy did not control the disease. The patient died 7 years after the initial diagnosis. CONCLUSIONS This case highlights the importance of the histopathology diagnosis in cases of testicular masses, and that sporadic, multifocal, and bilateral LCCSCTs present in younger men can be malignant despite the benign characteristics of the primary tumor.

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37岁男性双侧多灶性睾丸大细胞钙化支持细胞恶性肿瘤,表现为无痛性睾丸肿块。
背景:大细胞钙化支持细胞瘤(LCCSCT)属于性索间质肿瘤,极为罕见。睾丸lccsct表现为良性或恶性,偶尔出现,或与遗传综合征有关。良性lccsct多为双侧和多灶性,多发生于年轻患者。当患者有晚期或转移性疾病时,预后较差。然而,由于其罕见性,文献提供的关于其临床过程和治疗方案的证据很弱。本报告描述一位37岁男性患双侧多灶性恶性睾丸LCCSCT,表现为无痛性睾丸肿块。病例报告一名37岁男性双侧无痛性睾丸肿块。图像显示双侧大睾丸炎伴多灶睾丸内高回声和低信号病变。他接受了保留睾丸的手术,切除了1个睾丸病变。解剖病理分析显示LCCSCT的组织学特征显示为良性肿瘤。因此建议采取简单的后续行动。确诊后6年,患者出现淋巴结转移,行双侧睾丸根治术和淋巴结根治术。几个月后,出现胸膜、肺和骨转移。化疗和免疫治疗均不能控制病情。患者在初次诊断后7年死亡。结论:本病例强调了组织病理学诊断在睾丸肿块病例中的重要性,尽管原发肿瘤具有良性特征,但年轻男性中出现的散发性、多灶性和双侧lccsct可能是恶性的。
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来源期刊
American Journal of Case Reports
American Journal of Case Reports Medicine-Medicine (all)
CiteScore
1.80
自引率
0.00%
发文量
599
期刊介绍: American Journal of Case Reports is an international, peer-reviewed scientific journal that publishes single and series case reports in all medical fields. American Journal of Case Reports is issued on a continuous basis as a primary electronic journal. Print copies of a single article or a set of articles can be ordered on demand.
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