[成人期首次表现的持续性苗勒管综合征]
[Syndrome of persisting mullerian duct with first manifestation in an adult].
作者信息
Zastrow S, Nippgen J, Manseck A, Wirth M P
机构信息
Klinik und Poliklinik für Urologie, Universitätsklinikum "Carl Gustav Carus", Technische Universität Dresden.
出版信息
Aktuelle Urol. 2004 Nov;35(6):502-4. doi: 10.1055/s-2004-830029.
INTRODUCTION
We report on a 22-year-old male patient who presented with an intrapelvic tumor.
CASE REPORT
CT and MRI showed a left pelvic abscess, which was drained. After regression of the abscess, we removed the causative tubular structure surgically, revealing a rudimentary genital structure with parts of the Mullerian and Wolffian ducts.
CONCLUSIONS
This case report demonstrates an abscess formation as complication of a previously asymptomatic rudimentary genital structure, which was associated with further abnormalities, such as left testicular agenesia, perineoscrotal hypospadias and transverse testicular ectopia.
引言
我们报告了一名22岁男性患者，其患有盆腔内肿瘤。
病例报告
CT和MRI显示左侧盆腔脓肿，已进行引流。脓肿消退后，我们手术切除了致病的管状结构，发现了一个具有部分苗勒管和中肾管的发育不全的生殖结构。
结论
本病例报告显示，脓肿形成是先前无症状的发育不全生殖结构的并发症，该结构还伴有其他异常，如左侧睾丸缺如、会阴阴囊型尿道下裂和睾丸横位异位。
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