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耻骨下软骨性假囊肿:具有泌尿外科后果的骨科特征。

Subpubic cartilaginous pseudocyst: orthopedic feature with urological consequences.

作者信息

Farag Fawzy, van der Geest Ingrid, Hulsbergen-van de Kaa Christina, Heesakkers John

机构信息

Department of Urology, Radboud University Medical Centre, P.O. Box 9101, 6500 HB Nijmegen, The Netherlands ; Department of Urology, Sohag University Hospitals, Egypt.

Department of Orthopedic Surgery, Radboud University Medical Centre, The Netherlands.

出版信息

Case Rep Urol. 2014;2014:176089. doi: 10.1155/2014/176089. Epub 2014 Jan 16.

Abstract

Introduction. Masses arising from structures adjacent to the female urethra can cause obstructive urinary symptoms. Subpubic cartilaginous pseudocyst is a rare degenerative lesion of pubic symphysis that may cause these symptoms. Materials and Methods. A 61-year- and 57-year-old women presented with symptoms of difficult micturition and dyspareunia. Physical examination revealed a painless smooth, rounded, firm, and cystic mass, at the anterior vaginal wall of about 4 cm width. The mass caused inward deviation of the external urethral meatus. Cystoscopy and MRI were done. Results. Cystoscopy of case 1 (61 y) demonstrated anterior external urethral compression with normal urethral mucosa. Cystoscopy was not possible in case 2 (57 y) because the urethra could not be entered under local anesthesia. MRI showed almost the same findings in both cases: midline, rounded, and cystic mass ~3 × 3 × 4 cm, anterosuperior to the urethra, and posteroinferior to the pubic symphysis, with normal features of the urinary bladder. Open surgical excision of theses lesions was performed in both patients. Histopathologic assessment of the specimen obtained from both patients showed degenerated hyaline with areas of fibrinous and mucoid degeneration, a picture suggestive of cartilaginous subpubic pseudocyst. After 11-month and 4-month followup of patients numbers 1 and 2, respectively, there is no evidence of local recurrence of the lesion, either clinically or radiologically and both patients void empty. Conclusions. Subpubic cartilaginous pseudocysts are rare benign lesions with only 13 cases were reported in the literature. Patients present with a spectrum of gynecological and/or urological manifestations. Sizable lesions severely compressing the urethra need surgical excision to restore the voiding function.

摘要

引言。起源于女性尿道相邻结构的肿物可导致梗阻性尿路症状。耻骨下软骨假性囊肿是耻骨联合的一种罕见退行性病变,可引起这些症状。

材料与方法。一名61岁和一名57岁女性出现排尿困难和性交困难症状。体格检查发现阴道前壁有一个无痛、光滑、圆形、质地硬且呈囊性的肿物,宽约4厘米。该肿物导致尿道外口向内移位。进行了膀胱镜检查和磁共振成像(MRI)。

结果。病例1(61岁)的膀胱镜检查显示尿道外口前方受压,尿道黏膜正常。病例2(57岁)因在局部麻醉下无法进入尿道而未进行膀胱镜检查。MRI在两个病例中显示几乎相同的结果:中线处、圆形、囊性肿物,大小约为3×3×4厘米,位于尿道前上方、耻骨联合后下方,膀胱形态正常。两名患者均接受了这些病变的开放性手术切除。对两名患者获取的标本进行组织病理学评估显示,有透明质退变区域伴有纤维蛋白样和黏液样变性,这一表现提示耻骨下软骨假性囊肿。分别对患者1和患者2进行11个月和4个月的随访后,临床及影像学检查均未发现病变局部复发的证据,且两名患者均能排空尿液。

结论。耻骨下软骨假性囊肿是罕见的良性病变,文献中仅报道了13例。患者表现出一系列妇科和/或泌尿系统症状。较大的病变严重压迫尿道时需要手术切除以恢复排尿功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5ac/3914336/606c3e445565/CRIM.UROLOGY2014-176089.001.jpg

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