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Subpubic cartilaginous cyst: a rare cause of vulvar lesion

机译:耻骨下软骨囊肿:外阴病变的罕见原因

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A 67-year-old postmenopausal, multiparous female pre sented with a one-month history of vulvar edema, with no vaginal bleeding or dysuria, reporting only local discomfort. A solid, fixed, painless nodule was found on her vulva. Magnetic resonance imaging (MRI) showed an oval fibrous mass, with a hypointense signal in T1-weighted sequences and a hetero geneous, predominantly hyperintense signal in T2-weighted sequences (Figure 1). The formation showed thick walls and contrast enhancement, with no restricted diffusion. It was in close contact with the lower edge of the symphysis pubis and measured 2.8 × 2.5 × 2.3 cm. Based on the MRI findings and the location of the lesion, we considered a diagnosis of subpubic cartilaginous cyst (SCC).
机译:一名67岁的绝经后多胎女性,有一个月的外阴浮肿史,无阴道出血或排尿困难,仅报告局部不适。在她的外阴上发现了坚实,固定,无痛的结节。磁共振成像(MRI)显示椭圆形的纤维团,在T1加权序列中有一个低信号,在T2加权序列中有一个异质的,主要是高强度信号(图1)。地层显示出厚壁和对比增强,没有限制扩散。它与耻骨联合的下边缘紧密接触,尺寸为2.8×2.5×2.3 cm。基于MRI的发现和病变的位置,我们考虑了耻骨下软骨囊肿(SCC)的诊断。

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