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Superficial acral fibromyxoma: A rare and distinct clinicopathological entity: A case report and review of literature

机译:浅表性肺纤维瘤:一种罕见且独特的临床病理学实体:一例病例报告并文献复习

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摘要

Superficial acral fibromyxoma (SAF) is a rare, slow growing soft tissue tumor which was first described as a separate entity in 2001 by Fetsch et al. The tumor involves periungual and subungual regions of fingers and toes in middle aged adults with slight male predominance. Not many cases have been reported worldwide. To the best of our knowledge, only a couple of such cases have been reported earlier in Indian population. Superficial acral fibromyxoma has a recurrence rate of 25%. Local recurrence is almost always associated with positive margins. Malignant or metastatic behaviour has not been reported as yet. Since the tumor has a tendency to recur, it is beneficial to make a pre-operative provisional diagnosis and do wide surgical excision with tumor free margins and keep the patient on regular follow up.
机译:浅表性纤维纤维瘤(SAF)是一种罕见的,生长缓慢的软组织肿瘤,Fetsch等人于2001年首次将其描述为一个单独的实体。在中年成年人中,该肿瘤累及手指和脚趾的趾周围和趾下区域,男性占主导地位。全世界报道的病例并不多。据我们所知,在印度人口中,仅早些时候报道了这种情况。浅表端纤维纤维瘤的复发率为25%。局部复发几乎总是与正切缘相关。尚未报告恶性或转移性行为。由于肿瘤有复发的趋势,因此有利于进行术前临时诊断,并在无肿瘤边缘的情况下进行广泛的手术切除,并使患者保持定期的随访。

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