Raveenthiran综合征——Spigelian疝内异位睾丸:几点补充意见

Q4 Medicine Journal of Neonatal Surgery Pub Date : 2021-09-09 DOI:10.47338/jns.v10.1024
Venkatachalam Raveenthiran
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引用次数: 0

摘要

我怀着极大的兴趣阅读了Sinacer等人关于先天性Spigelian疝与隐睾、多指畸形和肛门狭窄之间关系的文章虽然这种关联早在1895年就已为人所知,但直到2005年才被认为是一种新的综合征。[2,3]从那时起,人们对这一临床实体的认识越来越高2015年Moles-Morenilla等人将其命名为“Raveenthiran综合征”,并将其分为两种类型:1型是Spigelian疝和异位睾丸的独家关联,2型是Spigelian疝和异位睾丸合并其他异常据此,Sinacer等报道的新生儿属于2型Raveenthiran综合征。
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The Raveenthiran Syndrome—Ectopic testis within Spigelian hernia: Few additional remarks
I read, with great interest, the article by Sinacer et al. on the association of congenital Spigelian hernia with cryptorchidism, polydactyly, and anal stenosis.[1] Although this association is known since 1895, only in 2005 it was recognized as a new syndrome.[2,3] Since then there has been an increasing awareness about this clinical entity.[4] In 2015 Moles-Morenilla et al. named it ‘Raveenthiran syndrome’ and classified it into two types: type-1 is an exclusive association of Spigelian hernia and ectopic testis while type-2 is Spigelian hernia and ectopic testis associated with other anomalies.[5] Accordingly, the newborn reported by Sinacer et al. belongs to type-2 Raveenthiran syndrome.
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来源期刊
Journal of Neonatal Surgery
Journal of Neonatal Surgery Medicine-Surgery
CiteScore
0.30
自引率
0.00%
发文量
29
审稿时长
6 weeks
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