2型5 α还原酶缺乏症患者睾丸组织学分析:与无内分泌异常患者隐睾睾丸的比较及文献复习

IF 1 Q4 ENDOCRINOLOGY & METABOLISM
Clinical Pediatric Endocrinology Pub Date : 2022-01-01 Epub Date: 2022-06-03 DOI:10.1297/cpe.2022-0025
Tamaki Wada, Chihiro Ichikawa, Makoto Takeuchi, Futoshi Matsui, Fumi Matsumoto, Shinobu Ida, Yuri Etani, Masanobu Kawai
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引用次数: 0

摘要

婴儿期睾丸的完整组织学证明,5α还原酶2型缺乏(5α rd)的个体在产前睾丸分化是正常的;然而,这些个体中的大多数在成年期患有无精子症或少精子症,这表明精子发生受损发生在出生后。虽然伴随的隐睾症可能是这一过程的部分原因,但潜在的机制仍不清楚。为了解决这个问题,我们回顾性地比较了一名3岁患者和一名18岁5αRD患者睾丸下降的组织学结果。在后者中,睾丸组织学与从5名没有内分泌异常的青少年患者获得的隐睾睾丸进行比较。3岁患者的组织学检查结果显示生殖细胞数量正常,精小管完整。相比之下,一名18岁的患者表现出生殖细胞数量明显减少和精管萎缩。这些发现与在没有内分泌异常的隐睾中观察到的结果非常相似。这些发现表明,5αRD患者生殖细胞减少可能至少部分是由伴随的隐睾引起的。由于生殖细胞数量在婴儿时期并没有减少,建议尽早进行睾丸切除术,以防止生殖细胞数量减少,保持生育能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Histological analysis of testes in patients with 5 alpha-reductase deficiency type 2: Comparison with cryptorchid testes in patients without endocrinological abnormalities and a review of the literature.

Histological analysis of testes in patients with 5 alpha-reductase deficiency type 2: Comparison with cryptorchid testes in patients without endocrinological abnormalities and a review of the literature.

Histological analysis of testes in patients with 5 alpha-reductase deficiency type 2: Comparison with cryptorchid testes in patients without endocrinological abnormalities and a review of the literature.

Histological analysis of testes in patients with 5 alpha-reductase deficiency type 2: Comparison with cryptorchid testes in patients without endocrinological abnormalities and a review of the literature.

As evidenced by the intact histology of the testes during infancy, testicular differentiation during the prenatal period occurs normally in individuals with 5 alpha-reductase type 2 deficiency (5αRD); however, a majority of these individuals suffer from azoospermia or oligospermia during adulthood, indicating that impaired spermatogenesis occurs postnatally. Although the accompanying cryptorchidism may be partly responsible for this process, the underlying mechanisms remain largely unknown. To address this issue, we retrospectively compared the histological findings of descended testes in a 3-mo-old patient and undescended testes in an 18-yr-old patient with 5αRD. In the latter, testicular histology was compared to that of cryptorchid testes obtained from five adolescent patients without endocrinological abnormalities. Histological findings of a 3-mo-old patient revealed normal number of germ cells with intact seminiferous tubules. In contrast, an 18-yr-old patient showed marked reduction in germ cell number and atrophic seminiferous tubules. The findings were very similar to those observed in cryptorchid testes without endocrinological abnormalities. These findings suggest that the decrease in germ cells in 5αRD patients may be at least partly caused by accompanying cryptorchidism. As the number of germ cells did not decrease during the infantile period, early orchiopexy is recommended to prevent a decrease in germ cell number and preserve fertility.

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来源期刊
Clinical Pediatric Endocrinology
Clinical Pediatric Endocrinology ENDOCRINOLOGY & METABOLISM-
CiteScore
2.40
自引率
7.10%
发文量
34
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