Xing Ren-Wei, Nie Han-Qiu, Zhou Xian-Fei, Zhang Fang-Fang, Mou Yong-Hua
Department of Hepatobiliary Surgery, Taizhou Municipal Hospital, Taizhou 318000, Zhejiang Province, China.
Department of Pathology, Taizhou Municipal Hospital, Taizhou 318000, Zhejiang Province, China.
World J Clin Cases. 2022 Feb 26;10(6):1922-1928. doi: 10.12998/wjcc.v10.i6.1922.
Proliferative myositis is a rare benign tumor that is typically self-limiting and does not become malignant. It can be cured by simple resection without reported recurrence. Due to its rapid growth, hard structure and ill-defined borders, it can however be mistaken for malignant tumors such as sarcomas.
We investigate the case of a 64-year-old male with proliferative myositis of the abdominal wall, who was preoperatively administered a needle aspiration biopsy and given a simple excision and patch repair. We then compared it with other similar cases to determine the effectiveness of this treatment method.
Resection with follow-up observation has shown to be an effective treatment method for proliferative myositis. To avoid unnecessarily extended or destructive resection, a thorough and conclusive diagnosis is crucial, which requires adequate imaging and pathological knowledge.
增殖性肌炎是一种罕见的良性肿瘤，通常具有自限性，不会恶变。通过简单切除即可治愈，未见复发报道。然而，由于其生长迅速、质地坚硬且边界不清，它可能被误诊为肉瘤等恶性肿瘤。
我们研究了一名64岁腹壁增殖性肌炎男性患者的病例，该患者术前接受了针吸活检，并进行了简单切除和补片修补。然后我们将其与其他类似病例进行比较，以确定这种治疗方法的有效性。
切除并随访观察已被证明是治疗增殖性肌炎的有效方法。为避免不必要的扩大或破坏性切除，进行全面而确切的诊断至关重要，这需要足够的影像学和病理学知识。
