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真两性畸形：成年人的噩梦。

True hermaphroditism: A nightmare for an adult.

作者信息

Vishwakarma Ranjit B, Gite Venkat A, Shaw Vivek, Sharma Shashank

机构信息

Department of Urology, Grant Government Medical College & Sir JJ Hospital, Mumbai, India.

出版信息

Curr Urol. 2024 Dec;18(4):344-346. doi: 10.1097/CU9.0000000000000202. Epub 2024 Dec 20.

DOI:10.1097/CU9.0000000000000202
PMID:40256289
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12005016/
Abstract

The disorder of sex development is a rare disorder that usually occurs in early childhood. As adults, those with disorder of sexual development present with gynecomastia, primary amenorrhea, and primary infertility, which often causes great psychological impact. We report a unique case of a male adult hermaphrodite presenting with hematometra and hematosalpinx. Early management including psychiatry counseling, gender reassignment, and surgery is essential. Our patient underwent müllerian tissue removal with phallus reconstruction.

摘要

性发育障碍是一种罕见的疾病，通常发生在儿童早期。成年后，患有性发育障碍的人会出现男性乳房发育、原发性闭经和原发性不孕，这往往会造成巨大的心理影响。我们报告了一例独特的男性假两性畸形成年患者，其表现为子宫积血和输卵管积血。早期管理包括心理咨询、性别重新认定和手术，这至关重要。我们的患者接受了苗勒管组织切除和阴茎重建手术。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da39/12005016/f618fda3e36a/curr-urol-18-344-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da39/12005016/bc79c04c0c4f/curr-urol-18-344-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da39/12005016/fef4c13352bc/curr-urol-18-344-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da39/12005016/dbf64bf491a2/curr-urol-18-344-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da39/12005016/6f9c51c64bb3/curr-urol-18-344-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da39/12005016/01af7a122056/curr-urol-18-344-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da39/12005016/0ca38e57fefa/curr-urol-18-344-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da39/12005016/f618fda3e36a/curr-urol-18-344-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da39/12005016/bc79c04c0c4f/curr-urol-18-344-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da39/12005016/fef4c13352bc/curr-urol-18-344-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da39/12005016/dbf64bf491a2/curr-urol-18-344-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da39/12005016/6f9c51c64bb3/curr-urol-18-344-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da39/12005016/01af7a122056/curr-urol-18-344-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da39/12005016/0ca38e57fefa/curr-urol-18-344-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da39/12005016/f618fda3e36a/curr-urol-18-344-g007.jpg

相似文献

1
True hermaphroditism: A nightmare for an adult.真两性畸形：成年人的噩梦。
Curr Urol. 2024 Dec;18(4):344-346. doi: 10.1097/CU9.0000000000000202. Epub 2024 Dec 20.
2
True hermaphroditism presenting as bilateral gynecomastia in an adolescent phenotypic male.在一名青春期表型男性中表现为双侧乳腺增生的真两性畸形。
Fertil Steril. 2005 Apr;83(4):1041. doi: 10.1016/j.fertnstert.2004.09.036.
3
Secondary pyosalpinx after reconstructive surgery of vaginal agenesis patient with bilateral hematosalpinx: A case report.阴道闭锁患者双侧输卵管积血重建手术后继发输卵管积脓：一例报告
Int J Surg Case Rep. 2021 Aug;85:106166. doi: 10.1016/j.ijscr.2021.106166. Epub 2021 Jul 2.
4
True hermaphroditism. A case report with observations on its bizarre presentation.
S Afr Med J. 1984 Dec 1;66(22):855-8.
5
A case of true hermaphroditism presenting as a testicular tumour.一例表现为睾丸肿瘤的真两性畸形病例。
Case Rep Urol. 2015;2015:598138. doi: 10.1155/2015/598138. Epub 2015 Feb 3.
6
Uterine conserving surgery in a case of cervicovaginal agenesis with unicornuate uterus.单角子宫合并宫颈阴道发育不全病例中的子宫保留手术。
J Hum Reprod Sci. 2016 Oct-Dec;9(4):267-270. doi: 10.4103/0974-1208.197696.
7
Primary amenorrhea and virilization in a true hermaphrodite with a rare dicentric Y chromosome.一名具有罕见双着丝粒Y染色体的真两性畸形患者出现原发性闭经和男性化。
Obstet Gynecol. 1984 Sep;64(3 Suppl):64S-67S. doi: 10.1097/00006250-198409001-00017.
8
Laparoscopy-assisted Neocervicovaginal Reconstruction in a Rare Case of Müllerian Anomaly: Cervicovaginal Aplasia with Unicornuate Uterus.腹腔镜辅助下罕见 Müllerian 异常的新阴道重建：宫颈阴道发育不全伴单角子宫。
J Minim Invasive Gynecol. 2020 Sep-Oct;27(6):1261-1262. doi: 10.1016/j.jmig.2019.12.008. Epub 2019 Dec 13.
9
Late-onset hematometra and hematosalpinx in a woman with a noncommunicating uterine horn. A case report.一名子宫角不通的女性出现迟发性子宫积血和输卵管积血。病例报告。
J Reprod Med. 1998 May;43(5):465-7.
10
True hermaphrodite: very unusual type.
Ethiop Med J. 2004 Jul;42(3):221-8.

本文引用的文献

1
Pregnancy in true hermaphrodites and all male offspring to date.真两性畸形患者的妊娠情况及迄今为止所有的男性后代。
Obstet Gynecol. 2009 Feb;113(2 Pt 2):534-536. doi: 10.1097/AOG.0b013e3181866456.
2
Sex determination and differentiation.性别决定与分化。
N Engl J Med. 2004 Jan 22;350(4):367-78. doi: 10.1056/NEJMra022784.
3
True hermaphroditism and normal male external genitalia: a rare presentation.
Acta Paediatr. 1999 Aug;88(8):909-11. doi: 10.1080/08035259950168865.
4
True hermaphroditism: geographical distribution, clinical findings, chromosomes and gonadal histology.真两性畸形：地理分布、临床发现、染色体及性腺组织学
Eur J Pediatr. 1994 Jan;153(1):2-10. doi: 10.1007/BF02000779.
5
Preservation of gonadal function in true hermaphroditism.真两性畸形中生殖腺功能的保留
J Pediatr Surg. 1984 Feb;19(1):50-5. doi: 10.1016/s0022-3468(84)80015-9.
6
True hermaphroditism presenting as intermittent hematuria and groin pain.
Urology. 1986 Aug;28(2):133-6. doi: 10.1016/0090-4295(86)90105-6.
7
Gonadoblastoma in a true hermaphrodite with a 46,XX karyotype.核型为46,XX的真两性畸形患者中的性腺母细胞瘤。
Obstet Gynecol. 1976 Mar;47(3):355-8.