阴囊皮纤维肉瘤突起:曼昆学术医院病例回顾

Lerato Hector Nong, F. Makhandule, Dumisa Ntshani, Mirza Bhuiyan
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摘要

背景:皮纤维肉瘤(DFSP)是一种不常见的生长缓慢的软组织肿瘤。皮纤维肉瘤在人群中的总发病率为 0.3-5/百万,黑人比白人更常见,男性和女性的发病率相同。本病例报告的主要目的是分享我们治疗皮纤维肉瘤突起的经验,并就标准治疗方法进行文献综述:一名 28 岁男性因右侧阴囊内无痛性肿块就诊 5 年。体格检查时,肿块呈分叶状,与下层组织固定,无触痛,大小为 8 X 8 厘米,未触及腹股沟淋巴结。超声波检查显示这是一个血管丰富的软组织肿瘤,没有累及睾丸。对肿瘤进行了大范围局部切除,组织学检查显示肿瘤为突起的溃疡性结节。胸部和腹部的分期 CT 扫描结果正常,未发现任何转移病灶:结论:DFSP是一种生长缓慢、局部侵袭性强的肿瘤。结论:DFSP 是一种生长缓慢、局部侵袭性强的肿瘤,因此,早期诊断和彻底手术切除可使患者痊愈。莫氏显微外科手术能彻底清除肿瘤,因此已成为治疗 DFSP 的首选方法。伊马替尼(Imatinib)是一种新型的 DFSP 治疗方法,目前正得到越来越多的应用。
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Scrotal Dermatofibrosarcoma Protuberance: A Case Review at Mankweng Academic Hospital
Background: Dermatofibrosarcoma Protuberance (DFSP) is an uncommon slow-growing soft tissue tumour. The overall incidence of DFSP in the population ranges from 0.3–5 per million and is more common in blacks than whites, males and females are affected equally. The main objective of this case report is to share our experience with Dermatofibrosarcoma Protuberance and give a literature review on the standard of care. Case Presentation: A 28-year-old male presented to the outpatient department with a five-year history of a painless right inguinoscrotal mass. On physical examination the mass was lobulated, fixed to the underlying tissue, it was non-tender measured 8 X 8 cm and there were no inguinal lymph nodes palpable. Ultrasound showed a hypervascular soft tissue tumour not involving the testicle. Wide Local Excision was performed, and histology showed a protuberant ulcerated nodule. A staging CT scan of the chest and abdomen was normal with no features of any metastatic lesions. Conclusion: DFSP is a slow-growing and locally aggressive tumor. Therefore, early diagnosis and complete surgical resection can result in patients being cured. Mohs micrographic surgery is becoming the treatment of choice for DFSP as it results in complete surgical clearance. Imatinib is a novel treatment option for DFSP and is increasingly being used.
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