手术切除治疗一例罕见的持续性苗勒管综合征。

Iwens Moreira de Faria, Augusto Machado de Souza, Luiz Rodrigues Pereira Júnior, Gabriel Gomes Vieira Ribeiro Leite
{"title":"手术切除治疗一例罕见的持续性苗勒管综合征。","authors":"Iwens Moreira de Faria,&nbsp;Augusto Machado de Souza,&nbsp;Luiz Rodrigues Pereira Júnior,&nbsp;Gabriel Gomes Vieira Ribeiro Leite","doi":"10.1177/26330040231184484","DOIUrl":null,"url":null,"abstract":"<p><p>Persistent Mullerian Duct Syndrome (PMDS) is an extremely rare disease with less than 300 cases recorded in medical literature. Our patient was a 37 year old male who presented at the medical office with hematospermia as his sole complaint. He had previously undergone left orchidopexy and presented with hypotrophic left testicle and right testicle agenesis. PMDS differential was considered with the clear observation of a uterus-like structure during pelvic ultrasonography. The organs were later studied in magnetic resonance imaging and confirmed by post-surgery anatomopathological examination. Patient was discharged 24 h after surgery and developed azoospermia post-surgery.</p>","PeriodicalId":75218,"journal":{"name":"Therapeutic advances in rare disease","volume":"4 ","pages":"26330040231184484"},"PeriodicalIF":0.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/2c/b1/10.1177_26330040231184484.PMC10331220.pdf","citationCount":"0","resultStr":"{\"title\":\"Surgical resection therapy of a rare presentation of persistent Mullerian duct syndrome: a case review.\",\"authors\":\"Iwens Moreira de Faria,&nbsp;Augusto Machado de Souza,&nbsp;Luiz Rodrigues Pereira Júnior,&nbsp;Gabriel Gomes Vieira Ribeiro Leite\",\"doi\":\"10.1177/26330040231184484\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Persistent Mullerian Duct Syndrome (PMDS) is an extremely rare disease with less than 300 cases recorded in medical literature. Our patient was a 37 year old male who presented at the medical office with hematospermia as his sole complaint. He had previously undergone left orchidopexy and presented with hypotrophic left testicle and right testicle agenesis. PMDS differential was considered with the clear observation of a uterus-like structure during pelvic ultrasonography. The organs were later studied in magnetic resonance imaging and confirmed by post-surgery anatomopathological examination. Patient was discharged 24 h after surgery and developed azoospermia post-surgery.</p>\",\"PeriodicalId\":75218,\"journal\":{\"name\":\"Therapeutic advances in rare disease\",\"volume\":\"4 \",\"pages\":\"26330040231184484\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/2c/b1/10.1177_26330040231184484.PMC10331220.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Therapeutic advances in rare disease\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1177/26330040231184484\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Therapeutic advances in rare disease","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1177/26330040231184484","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

持续性苗勒管综合征(PMDS)是一种极为罕见的疾病,医学文献记录的病例不足300例。我们的病人是一名37岁的男性,他在医疗办公室以血精作为他唯一的主诉。他曾接受左睾丸切除术,表现为左睾丸萎缩和右睾丸发育不全。盆腔超声检查明确观察到子宫样结构,考虑PMDS的鉴别。经磁共振成像及术后解剖病理检查证实。患者术后24 h出院,术后出现无精子症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Surgical resection therapy of a rare presentation of persistent Mullerian duct syndrome: a case review.

Surgical resection therapy of a rare presentation of persistent Mullerian duct syndrome: a case review.

Surgical resection therapy of a rare presentation of persistent Mullerian duct syndrome: a case review.

Surgical resection therapy of a rare presentation of persistent Mullerian duct syndrome: a case review.

Persistent Mullerian Duct Syndrome (PMDS) is an extremely rare disease with less than 300 cases recorded in medical literature. Our patient was a 37 year old male who presented at the medical office with hematospermia as his sole complaint. He had previously undergone left orchidopexy and presented with hypotrophic left testicle and right testicle agenesis. PMDS differential was considered with the clear observation of a uterus-like structure during pelvic ultrasonography. The organs were later studied in magnetic resonance imaging and confirmed by post-surgery anatomopathological examination. Patient was discharged 24 h after surgery and developed azoospermia post-surgery.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
2.00
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信