New classification of the penoscrotal positional anomalies

IF 1.6 4区 医学 Q4 DEVELOPMENTAL BIOLOGY Birth Defects Research Pub Date : 2024-07-13 DOI:10.1002/bdr2.2376
Mohamed A. Baky Fahmy, Ayman Altramsy, Mohammed Abdel-Latif M. Ayad
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Abstract

Background

The aspect of sexual differentiation and the mechanism controlling the position of genitalia, which represents one of the most substantial differences between the sexes, is still poorly understood. Minor cases and some variants of penoscrotal transposition (PST) are unreported, and obvious cases were classified broadly and confused with other unrelated anomalies.

Methodology

Relevant literature published till 2022 were reviewed then organized, recapitulated, and presented in comparison with the findings and data of 65 child diagnosed with PST. So, an integrated comprehensive approach to this uncommon condition enabled a new classification including few unreported variant cases, which were complemented.

Results

PST is classified herein into a cephalic or caudal scrotal migration, the cephalic type subdivided into major and minor subtypes the latter type subdivided into bilateral, unilateral or central subtypes. Cases of caudal scrotal regression is an unreported anomaly in which the scrotum located caudally, as constant association with epispadias/exstrophy anomalies leaving a wide distance between the fixed penis and the scrotal sacs.

Conclusion

PST is not rare as it was believed, it occurs in two directions; cephalic and caudal directions. Scrotal caudal regression anomaly was not described before, as well the PST presented as an inguinal hernia.

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阴茎阴囊位置异常的新分类。
背景:性分化和控制生殖器位置的机制是两性之间最显著的差异之一,但人们对这一问题的了解仍然很少。阴茎阴囊转位(PST)的轻微病例和一些变异病例未见报道,明显的病例被笼统归类,并与其他无关的异常病例混淆:方法:对截至 2022 年发表的相关文献进行回顾,然后进行整理、概括,并与 65 例确诊为 PST 的患儿的研究结果和数据进行对比。因此,对这一罕见病症的综合全面的方法使得新的分类方法成为可能,其中包括一些未报道的变异病例,并对其进行了补充:结果:PST 在此被分为头侧或阴囊尾侧移位,头侧移位又分为主要亚型和次要亚型,后者又分为双侧、单侧或中央亚型。阴囊尾端回缩是一种未报告的异常情况,阴囊位于尾端,与阴茎外展/萎缩异常常伴有关联,在固定的阴茎和阴囊之间留有较宽的距离:PST并不像人们认为的那样罕见,它发生在两个方向:头侧和尾侧。阴囊尾部回缩异常以前从未被描述过,PST也表现为腹股沟疝。
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来源期刊
Birth Defects Research
Birth Defects Research Medicine-Embryology
CiteScore
3.60
自引率
9.50%
发文量
153
期刊介绍: The journal Birth Defects Research publishes original research and reviews in areas related to the etiology of adverse developmental and reproductive outcome. In particular the journal is devoted to the publication of original scientific research that contributes to the understanding of the biology of embryonic development and the prenatal causative factors and mechanisms leading to adverse pregnancy outcomes, namely structural and functional birth defects, pregnancy loss, postnatal functional defects in the human population, and to the identification of prenatal factors and biological mechanisms that reduce these risks. Adverse reproductive and developmental outcomes may have genetic, environmental, nutritional or epigenetic causes. Accordingly, the journal Birth Defects Research takes an integrated, multidisciplinary approach in its organization and publication strategy. The journal Birth Defects Research contains separate sections for clinical and molecular teratology, developmental and reproductive toxicology, and reviews in developmental biology to acknowledge and accommodate the integrative nature of research in this field. Each section has a dedicated editor who is a leader in his/her field and who has full editorial authority in his/her area.
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