頁籤選單縮合
題 名 | The Management of Multiple Extratesticular Scrotal Epidermoid Cysts--Case Report=多發性陰囊表皮樣囊腫--病例報告及文獻回顧 |
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作 者 | 黃仁穩; 陳宏彰; | 書刊名 | 臺灣整形外科醫學會雜誌 |
卷 期 | 26:2 2017.06[民106.06] |
頁 次 | 頁206-212 |
分類號 | 416.275 |
關鍵詞 | 多發性陰囊表皮樣囊腫; 陰囊腫瘤; Multiple scrotal epidermoid cysts; Scrotal mass; |
語 文 | 英文(English) |
中文摘要 | 背景:表皮樣囊腫為一常見的疾病。然而,多發性陰囊表皮樣囊腫則相對罕見。目的及目標:此病例報告發表一例罕見的多發性陰囊表皮樣囊腫,且其位於睪丸外。除了病例報告,亦整理相關鑑別診斷,診斷工具及治療方法。材料及方法:此病例為一53歲男性病患,自述陰囊腫瘤已有超過30年之久,近年來逐漸變大。超音波診斷為低回音性病灶,尿液檢查,αFP,及β-hCG皆為正常。所有病灶皆切除乾淨,傷口直接縫合。病理報告為多發性表皮樣囊腫。結果:病患術後傷口癒合狀況良好。結論:多發性陰囊表皮樣囊腫則相當罕見,超音波及核磁共振可為診斷工具,標準治療方法須完全切除送病理化驗。 |
英文摘要 | Background: Epidermoid cysts are common benign skin lesions, but scrotal extratesticular epidermoid inclusion cysts (EIC) are rare. They are usually slow growing and non-tender. This is an extensive case of EIC which can present a challenge both in excision and reconstruction of this disease. Aim and objectives: We present a rare case of multiple scrotal extratesticular epidermoid cysts (a total of 22 EICs) as well as a review of the diagnosis, evaluation and management of this disease Materials and methods: A 53-year-old male presented with multiple scrotal mass for more than 30 years. He had no underlying disease and trauma history. Sonography revealed multiple hypoechoic lesions. Urinalysis, alpha-fetoprotein (αFP), beta-human chorionic gonadotropin (β -hCG) and complete blood count were all within normal limits. Under the impression of a benign scrotal mass, complete excision was performed and the wound was closed primarily. Histological reports revealed a diagnosis of epidermoid cysts. Results: The wound healed well without wound dehiscence and infection after the operation. Conclusion: Multiple scrotal extra-testicular EICs are not often. Sonography and MRI can aid pre-operative diagnoses. Complete excision of the lesion for histological analysis confirms diagnosis and scrotal reconstruction can yield satisfying results both for the patient and the surgeon. |
本系統中英文摘要資訊取自各篇刊載內容。