Ahdoot Michael, Qadan Motaz, Santa-Maria Monica, Kennedy William A, Ilano Aaron
Stanford University Medical Center and Stanford University School of Medicine, Stanford, CA;
Can Urol Assoc J. 2013 Jan-Feb;7(1-2):E121-4. doi: 10.5489/cuaj.253.
A 32-year-old male presenting with a direct inguinal hernia was found to have uterine tissue extending through the inguinal canal, warranting a diagnosis of persistent Mullerian duct syndrome (PMDS). PMDS is an extremely rare form of internal male pseudo-hermaphroditism in which female internal sex organs, including the uterus, cervix and proximal vagina, persist in a 46XY male with normal external genitalia. The condition results from a congenital insensitivity to anti-Mullerian hormone, or lack of anti-Mullerian hormone, leading to persistence of the female internal sex organs in a male. Clinically, this condition is associated with cryptochoridism. Controversy persists regarding the appropriate treatment of PMDS, since resection of the remnant structures is associated with potential morbidity, but retention risks development of occasional malignancies. We review the literature and discuss various aspects of pathophysiology, diagnosis, and management of PMDS.
一名32岁患有直疝的男性被发现有子宫组织延伸至腹股沟管,确诊为持续性苗勒管综合征(PMDS)。PMDS是一种极其罕见的男性体内假性两性畸形,在具有正常外生殖器的46XY男性中,女性内生殖器(包括子宫、宫颈和近端阴道)持续存在。这种情况是由于对抗苗勒管激素先天性不敏感或缺乏抗苗勒管激素,导致女性内生殖器在男性体内持续存在。临床上,这种情况与隐睾症有关。关于PMDS的适当治疗仍存在争议,因为切除残余结构有潜在的发病率,但保留则有发生偶发恶性肿瘤的风险。我们回顾文献并讨论PMDS病理生理学、诊断和管理的各个方面。