外阴皮肤纤维肉瘤隆突,一个不寻常的解剖位置。

IF 0.5 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
BJR Case Reports Pub Date : 2025-05-29 eCollection Date: 2025-07-01 DOI:10.1093/bjrcr/uaaf030
Bano Alsaleh, Ahmed Alanzi, Mohamed Alsaleh, Ahmed Alsaleh, Fouad Aladel
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引用次数: 0

摘要

摘要外阴隆突性皮肤纤维肉瘤(DFSP)是一种罕见的疾病。到目前为止,文献报道的病例数量有限。在目前的情况下,我们讨论一个38岁的女性提出了一个痛苦的左外阴肿块。她有左外阴肿块切除术的病史,病理证实为良性梭形细胞上皮瘤。目前的肿块,从左大阴唇延伸到左臀襞,通过增强磁共振成像(MRI)进行评估,显示一个明确的分叶状病变,靠近尿道远端和阴蒂,没有明确的侵犯。患者接受了广泛的局部切除术,根治性外阴切除术和左侧腹股沟淋巴结切除术。术后出现发热、外阴肿胀、排尿困难等症状。后续MRI显示外阴肿块完全消退,无复发。组织病理学鉴定肿块为DFSP,所有手术切缘均为阴性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Vulvar dermatofibrosarcoma protuberans, an unusual anatomical location.

Vulvar dermatofibrosarcoma protuberans, an unusual anatomical location.

Vulvar dermatofibrosarcoma protuberans (DFSP) is a rare pathology. So far, only limited number of cases have been reported in literature. In the present case, we discuss a 38-year-old female presented with a painful left vulvar mass. She had a prior history of a left vulvar mass excision which was histopathologically confirmed as benign spindle cell epithelioma. The current mass, extending from the left labia majora to the left gluteal fold, was assessed via contrast-enhanced magnetic resonance imaging (MRI), revealing a well-defined, lobulated lesion with proximity to the distal urethra and clitoris without definite invasion. The patient underwent a wide local excision, radical vulvectomy, and left inguinofemoral lymphadenectomy. Postoperatively, she experienced fever, vulvar swelling, and dysuria. Follow-up MRI demonstrated total resolution of the vulvar mass and collection with no recurrence. Histopathology identified the mass as DFSP, with all surgical margins negative.

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BJR Case Reports
BJR Case Reports RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING-
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