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一名4岁男孩出现脾性腺融合并伴有副脾的病例。

A case of splenogonadal fusion accompanied by accessory spleen in a 4-year-old boy.

作者信息

Shakeri Aria, Shakeri Arash, Rasolmali Reza, Shakeri Saeed

机构信息

University of Virginia School of Medicine, Charlottesville, USA.

School of Pharmacy, Health Sciences Campus, University of Waterloo, Waterloo, Canada.

出版信息

Urol Ann. 2018 Oct-Dec;10(4):406-408. doi: 10.4103/UA.UA_194_17.

Abstract

Splenogonadal fusion (SGF) is a rare benign malformation in which spleen is aberrantly attached to the gonads or mesonephric derivatives. This entity often presents with scrotal mass, inguinal hernia, or cryptorchidism. Herein, we report our experience with a boy who presented with a scrotal enlargement which later turned out to be SGF. Moreover, an accessory spleen was unexpectedly found in the left inguinal canal. To the best of our knowledge, this is the first report of SGF and accessory spleen in the literature. Although rare, SGF should be included in the complete differential diagnosis list of scrotal masses, especially in children. The use of frozen section pathology if available would aid the surgeon in avoiding unnecessary orchiectomy in small testicular masses of benign origin.

摘要

脾性腺融合(SGF)是一种罕见的良性畸形,其中脾脏异常附着于性腺或中肾衍生物。该病症常表现为阴囊肿块、腹股沟疝或隐睾。在此,我们报告一名男孩的病例,他最初表现为阴囊肿大,后来确诊为脾性腺融合。此外,在左侧腹股沟管意外发现一个副脾。据我们所知,这是文献中首例关于脾性腺融合和副脾的报告。尽管罕见,但脾性腺融合应列入阴囊肿块的完整鉴别诊断清单中,尤其是在儿童中。如有条件,使用冰冻切片病理检查将有助于外科医生避免对良性起源的小睾丸肿块进行不必要的睾丸切除术。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eacc/6194785/807851694e86/UA-10-406-g001.jpg

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