Goldman Hariette, Sowter Steven
Wagga Wagga Base Hospital, Wagga Wagga, New South Wales, Australia.
Riverina Urology/Wagga Wagga Base Hospital, Wagga Wagga, New South Wales, Australia.
BMJ Case Rep. 2016 Jun 28;2016:bcr2015211807. doi: 10.1136/bcr-2015-211807.
Urachal adenocarcinoma is a rare non-urothelial malignancy that represents only 0.5% of all vesical cancers. Urachal adenocarcinoma most commonly occurs in the 5th to 7th decade. We describe a case of a 35-year-old woman (G3P1) who presented at 20 weeks pregnancy with two episodes of post-coital bleeding. Ultrasound demonstrated a uterine mass measuring 59×43×56 mm, presumed to be a leiomyoma. The decision was made to proceed to caesarean section at 38 weeks, given the progression of the presumed leiomyoma. A 2 cm bladder dome mass was incidentally discovered at the time of the caesarean section and an urgent intraoperative urology consult was sought. Resultantly, the bladder mass was dissected to the dome, and pathology returned urachal adenocarcinoma. This case report considers the treatment decisions involved when faced with urachal adenocarcinoma and reviews the literature surrounding this rare malignancy.
脐尿管腺癌是一种罕见的非尿路上皮恶性肿瘤,仅占所有膀胱癌的0.5%。脐尿管腺癌最常发生在50至70岁之间。我们报告一例35岁女性(G3P1),在妊娠20周时出现两次性交后出血。超声显示子宫有一个大小为59×43×56mm的肿块,推测为平滑肌瘤。鉴于推测的平滑肌瘤进展,决定在38周时进行剖宫产。剖宫产时偶然发现一个2cm的膀胱顶部肿块,并紧急寻求术中泌尿外科会诊。结果,将膀胱肿块切除至顶部,病理结果回报为脐尿管腺癌。本病例报告考虑了面对脐尿管腺癌时的治疗决策,并回顾了围绕这种罕见恶性肿瘤的文献。