Successful management of Leydig Cell Tumor in a 65-year-Old patient: A rare case report

IF 0.4 Q4 UROLOGY & NEPHROLOGY Urology Case Reports Pub Date : 2025-01-01 Epub Date: 2025-01-02 DOI:10.1016/j.eucr.2024.102927
Hasan Haydar , Ayham Qatza , Saja Karaja , Anagheem Alkhleef , Mohamad Yasin Lutfi , Habib Jarbouh
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Abstract

Leydig cell tumors (LCTs) are rare testicular neoplasms, representing 1–3% of all testicular tumors. A 65-year-old male presented with a painless left scrotal mass. Ultrasound revealed a 61 × 53 × 35 mm tumor with heterogeneous echogenicity and abundant blood supply. Radical orchidectomy was performed, and immunohistochemistry confirmed LCT with positivity for Inhibin A and calretinin, and negativity for CK, chromogranin, LCA, and low Ki67. Postoperative follow-up at 6 months showed improved condition, no scrotal masses, and normal tumor markers. Finally, LCTs in older males require differential diagnosis; hormonal activity impacts presentation. Conservative management and monitoring are crucial.
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65岁间质细胞瘤的成功治疗:一例罕见病例报告。
睾丸间质细胞瘤是一种罕见的睾丸肿瘤,约占所有睾丸肿瘤的1-3%。65岁男性,左侧阴囊无痛性肿块。超声示肿瘤61 × 53 × 35 mm,回声不均匀,血供丰富。行根治性兰花切除术,免疫组化证实LCT抑制素A和calretinin阳性,CK、嗜铬粒蛋白、LCA阴性,低Ki67。术后随访6个月病情好转,阴囊无肿块,肿瘤标志物正常。最后,老年男性的LCTs需要鉴别诊断;荷尔蒙活动影响表现。保守的管理和监测至关重要。
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来源期刊
Urology Case Reports
Urology Case Reports Medicine-Urology
CiteScore
0.90
自引率
20.00%
发文量
325
审稿时长
37 days
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