Quaba O, Evans A, Al-Nafussi A A, Nassan A
Department of Plastic Surgery, Ninewells University Hospital, Dundee DD1 9SY, UK.
Br J Plast Surg. 2005 Jun;58(4):561-4. doi: 10.1016/j.bjps.2004.03.006.
Superficial acral fibromyxoma is a rare soft tissue tumour affecting the digits, particularly the nail bed region. The condition was first described in 2001. We report the case of a 71-year-old man who presented with a long standing history of a lump affecting the pulp of the his right ring finger. This was surgically excised and subsequent pathological analysis confirmed the lesion to have been a superficial acral fibromyxoma. We use this case to highlight the features of this rare clinical entity, which has never previously been described in the surgical literature.
浅表性肢端纤维黏液瘤是一种罕见的软组织肿瘤,累及手指,尤其是甲床区域。该病于2001年首次被描述。我们报告一例71岁男性病例,其右环指指腹有一长期肿块。该肿块经手术切除,随后的病理分析证实病变为浅表性肢端纤维黏液瘤。我们通过这个病例来突出这种罕见临床实体的特征,而这在外科文献中此前从未有过描述。