Ghareeb George M, Grabemeyer Heidi, Dietrich Emily, Heisler Christine A
Michigan State University College of Human Medicine, Grand Rapids, MI, USA.
Female Pelvic Med Reconstr Surg. 2013 Jan-Feb;19(1):58-60. doi: 10.1097/SPV.0b013e318278cd3b.
A subpubic cartilaginous cyst is a rare and therefore poorly understood pathologic process involving the symphysis pubis. We describe a case of a postmenopausal female with acute urinary retention secondary to a periurethral cyst, and provide a literature review of previously reported cases of women with presenting complaints of a vulvar mass or pain. The differential diagnoses of a subpubic cartilaginous cyst, as well as management options, are discussed.
A 68-year-old woman presented with acute urinary retention. Physical examination revealed a 4-cm tender cystic mass palpated along the anterior vaginal wall traversing toward the posterior pubic ramus. A pelvic magnetic resonance imaging showed a 4.4 × 3.5 × 4.2-cm well-circumscribed, cystic lesion at the anterior aspect of the lower urethra with no intrinsic contrast enhancement. The cyst was surgically excised through a transvaginal approach with no recurrence to date.
A subpubic cartilaginous cyst is an uncommon lesion thought to originate from the symphysis pubis and to be a result of degenerative changes. Patients have presented with pain, a vulvar/vaginal mass, or both. This case describes a patient who presented with acute urinary retention. In patients with suspected subpubic cartilaginous cyst, the lesion may be excised in symptomatic patient or observed in those who are asymptomatic. Standard of care has not yet been determined regarding management due to the rarity of the lesion.
耻骨下软骨囊肿是一种罕见的、因而了解甚少的涉及耻骨联合的病理过程。我们描述一例绝经后女性因尿道周围囊肿继发急性尿潴留的病例,并对先前报道的以外阴肿块或疼痛为主诉的女性病例进行文献综述。讨论了耻骨下软骨囊肿的鉴别诊断以及治疗选择。
一名68岁女性因急性尿潴留就诊。体格检查发现沿阴道前壁可触及一个4厘米的压痛性囊性肿块,该肿块向耻骨后支延伸。盆腔磁共振成像显示在下尿道前方有一个4.4×3.5×4.2厘米边界清晰的囊性病变,无内部对比增强。通过经阴道途径手术切除囊肿,至今无复发。
耻骨下软骨囊肿是一种罕见的病变,被认为起源于耻骨联合,是退行性改变的结果。患者表现为疼痛、外阴/阴道肿块或两者皆有。本病例描述了一名以急性尿潴留就诊的患者。对于疑似耻骨下软骨囊肿的患者,有症状的患者可切除病变,无症状的患者可进行观察。由于该病变罕见,尚未确定其治疗的标准。