Testicular Torsion in a 14-Year-Old with Sertoli Cell Granular Cell Change and Sertoli Nodules.

IF 0.6 4区 医学 Q4 PATHOLOGY Fetal and Pediatric Pathology Pub Date : 2025-03-01 Epub Date: 2025-01-29 DOI:10.1080/15513815.2025.2458665
Randall Craver
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Abstract

Introduction: Sertoli eosinophilic granular change and Sertoli cell nodules are incidental findings. This details focal Sertoli eosinophilic granular and Sertoli cell only changes coincident with Sertoli cell nodules in a pubertal testis with acute torsion and bell clapper deformity. Case Report: A 14-year-old with bell clapper deformity underwent orchiectomy for torsion. There was acute interstitial hemorrhage. Seminiferous tubules contained only Sertoli cells in ∼10%, 2-5% of tubules demonstrated eosinophilic granular cell changes. There were several Sertoli cell nodules. Discussion: Sertoli cell nodules and eosinophilic granular change have not been described together. The focality of Sertoli cell only changes is unusual. The combination of focal Sertoli cell only and eosinophilic granular cell changes with Sertoli nodules in a testis with bell clapper abnormality may reflect an abnormal testicular environment, either physical and/or molecularly. This combination raises concerns for future fertility if seminiferous tubular abnormalities exist and progress in the remaining testis.

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14岁睾丸扭转伴支持细胞颗粒细胞改变及支持结节。
支持细胞嗜酸性颗粒改变和支持细胞结节是偶然发现的。此图详细描述了青春期睾丸急性扭转和钟瓣畸形中局灶性嗜酸性粒细胞颗粒和支持细胞仅与支持细胞结节一致的改变。病例报告:一个14岁的钟瓣畸形接受睾丸切除术扭转。急性间质出血。精精小管仅含支持细胞约10%,2-5%的小管表现出嗜酸性颗粒细胞的改变。可见几个支持细胞结节。讨论:支持细胞结节和嗜酸性颗粒性改变未被同时描述。支持细胞病灶的改变是不寻常的。铃状鼓膜异常的睾丸中,只有局灶性支持细胞和嗜酸性颗粒细胞的变化与支持细胞结节的结合可能反映了睾丸物理和/或分子环境的异常。这种组合引起了对未来生育能力的担忧,如果精管畸形存在并在剩余的睾丸中发展。
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来源期刊
CiteScore
3.00
自引率
0.00%
发文量
68
审稿时长
6-12 weeks
期刊介绍: Fetal and Pediatric Pathology is an established bimonthly international journal that publishes data on diseases of the developing embryo, newborns, children, and adolescents. The journal publishes original and review articles and reportable case reports. The expanded scope of the journal encompasses molecular basis of genetic disorders; molecular basis of diseases that lead to implantation failures; molecular basis of abnormal placentation; placentology and molecular basis of habitual abortion; intrauterine development and molecular basis of embryonic death; pathogenisis and etiologic factors involved in sudden infant death syndrome; the underlying molecular basis, and pathogenesis of diseases that lead to morbidity and mortality in newborns; prenatal, perinatal, and pediatric diseases and molecular basis of diseases of childhood including solid tumors and tumors of the hematopoietic system; and experimental and molecular pathology.
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