Testicular Cancer Unit, Department of Urology, Asklepios Klinik Altona, Paul Ehrlich Strasse 1, 22763, Hamburg, Germany.
Medizinisches Versorgungszentrum Hanse Histologikum, Fangdieckstrasse 75a, 22547, Hamburg, Germany.
J Med Case Rep. 2024 Feb 22;18(1):71. doi: 10.1186/s13256-024-04393-7.
Sex cord gonadal stromal tumors compose less than 10% of all testicular neoplasms and consist of a variety of histological subtypes. In 2016, the World Health Organization introduced a novel subtype, the myoid gonadal stromal tumor, that consists of spindle-shaped cells with immunohistologic features of muscle cells. Only few cases have been reported to date. Due to its rarity and owing to its only recent introduction, the current knowledge about myoid gonadal stromal tumor is limited, and particularly, appropriate clinical management is still ill-defined.
A 47-year-old man of Caucasian descent presented with nonspecific scrotal discomfort. A roundish and well demarcated hypoechoic mass of 8.5 mm in diameter was detected in the cranial region of the left testis. Serum tumor marker levels were within normal ranges. Testis-sparing surgery revealed a 9-mm whitish, hard mass with sharp surgical margin. Histologically, the neoplasm consisted of microfibrillar tissue with spindle-shaped cells harboring elongated nuclei. Immunohistochemical work-up disclosed expression of desmin, small muscle actin, and S100 protein giving evidence for the myogenic nature of the neoplastic cells. There was no indication of malignancy, neither histologically nor clinically. Follow-up of 1 year was uneventful.
A literature survey revealed 22 previous cases of myoid gonadal stromal tumor. The median age was 37 years, the median size of the neoplasm was 20 mm, and there was no side-preponderance. Myoid gonadal stromal tumor is not much different from other subtypes of gonadal stromal tumors nor from testicular gem cell tumors regarding age and laterality; however, tumor size is smaller in myoid gonadal stromal tumors than in germ cell tumors. Although rarely performed so far, testis-sparing surgery probably constitutes an appropriate treatment of this neoplasm. Myoid gonadal stromal tumor represents an emerging novel entity of benign testicular new growths that caregivers of patients with testicular tumors should be aware of.
性索-性腺间质肿瘤构成所有睾丸肿瘤的不到 10%,由多种组织学亚型组成。2016 年,世界卫生组织引入了一种新的亚型,即肌源性性腺间质肿瘤,由具有肌细胞免疫组织化学特征的梭形细胞组成。迄今为止,仅报道了少数病例。由于其罕见性以及最近才引入,目前对肌源性性腺间质肿瘤的了解有限,特别是适当的临床管理仍未明确。
一位 47 岁的白种人男性,因非特异性阴囊不适就诊。在左侧睾丸颅侧区域检测到一个 8.5 毫米直径的圆形、边界清晰的低回声肿块。血清肿瘤标志物水平在正常范围内。保留睾丸手术显示一个 9 毫米大小的、灰白色、硬实的肿块,手术切缘锐利。组织学上,肿瘤由微纤维组织组成,含有长梭形细胞核的梭形细胞。免疫组织化学检查显示结蛋白、小肌肉肌动蛋白和 S100 蛋白的表达,证明肿瘤细胞具有肌源性。无论是在组织学上还是临床上,都没有恶性的迹象。1 年的随访没有异常。
文献检索显示之前有 22 例肌源性性腺间质肿瘤的病例。中位年龄为 37 岁,肿瘤的中位大小为 20 毫米,无侧别优势。肌源性性腺间质肿瘤在年龄和侧别方面与其他性腺间质肿瘤或睾丸生殖细胞肿瘤没有太大区别;然而,肿瘤大小在肌源性性腺间质肿瘤中比在生殖细胞肿瘤中要小。尽管迄今为止很少进行,但保留睾丸手术可能是这种肿瘤的一种适当治疗方法。肌源性性腺间质肿瘤是一种新兴的良性睾丸新生物实体,应引起关注睾丸肿瘤患者的医护人员的注意。