外生殖器神经纤维瘤,阴蒂极度增大。

IF 0.7 Q4 UROLOGY & NEPHROLOGY
Urology Annals Pub Date : 2023-07-01 Epub Date: 2023-07-17 DOI:10.4103/ua.ua_86_22
Razan Almesned, Mohamed Alhagbani, Mohammed Sultan, Mohammed Alshayie, Naif Alqarni, Ahmed Alshammari
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引用次数: 0

摘要

泌尿生殖道神经纤维瘤病是罕见的,患病率为0.65%,涉及外生殖器的情况极为罕见。据报道,阴蒂、大阴唇和包皮的受累是最常见的。在此,我们报告了一个6岁女孩的病例,她被诊断为阴蒂神经纤维瘤;最大尺寸为9.4厘米。据我们所知,这是文献中报道的最大的阴蒂神经纤维瘤。由于此类病例的罕见性和文献报道的局限性,外生殖器神经纤维瘤的诊断需要医疗保健提供者的高度怀疑。手术切除和术后可能复发的随访仍然是治疗的黄金标准。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Neurofibroma of the external genitalia, extreme enlargement of the clitoris.

Neurofibroma of the external genitalia, extreme enlargement of the clitoris.

Neurofibroma of the external genitalia, extreme enlargement of the clitoris.

Neurofibroma of the external genitalia, extreme enlargement of the clitoris.

Neurofibromatosis of the genitourinary tract is rare, with a prevalence of 0.65%, and it is exceedingly rare to involve the external genitalia. Involvement of the clitoris, labia majora, and prepuce was reported with clitoromegaly being the most frequently occurring. Herein, we are reporting the case of a 6-year-old girl who was diagnosed with a neurofibroma of the clitoris; measuring 9.4 cm in its largest dimension. To the best of our knowledge, this is the largest clitoral neurofibroma reported in the literature. Due to the rarity of such cases and reports limitations in the literature, the diagnosis of neurofibroma of the external genitalia requires a high index of suspicion by health-care providers. Surgical excision and postoperative follow-up for possible recurrence remain the gold standard of management.

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来源期刊
Urology Annals
Urology Annals UROLOGY & NEPHROLOGY-
CiteScore
1.20
自引率
0.00%
发文量
59
审稿时长
31 weeks
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