Giant fibrokeratoma, a rare soft tissue tumor presenting like an accessory digit, a case report and review of literature.
Giant fibrokeratoma, a rare soft tissue tumor presenting like an accessory digit, a case report and review of literature.
复制标题
巨型纤维瘤是一种罕见的软组织肿瘤，像附件数字一样，病例报告和文献综述。
DOI：
10.1016/j.ijscr.2015.03.041
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发表时间：
2015
影响因子：
0.6
通讯作者：
Sunderamoorthy, D
中科院分区：
文献类型：
--
作者：
Ali, Mohammed;Mbah, C A;Alwadiya, Ahmed;Nur, Mutaz Mohammed;Sunderamoorthy, D
巨大的数字纤维角化瘤，指甲样变化，良性生长，手术切除。获得性数字纤维角化瘤是一种罕见的良性纤维肿瘤，通常作为孤立性病变发生在成人中，典型尺寸小于 1 厘米。一名 48 岁的非洲裔加勒比男子到我们的足部和脚踝诊所就诊，其左大脚趾远端指骨的足底有长期生长的肿瘤。生长过程很痛苦，影响了患者的活动能力。它的规模在17年的时间里逐渐扩大。生长物被完全切除，并通过二次意图使基部愈合。皮肤最终愈合了，患者得到了良好的治疗效果。组织学结果证实该生长物是指纤维角化瘤。由于数字纤维角化瘤的罕见性和该病例中肿瘤的独特形态外观，该病例引起人们的关注。此外，我们强调在鉴别诊断过程中排除异常生长的其他原因并考虑纤维角化瘤的重要性。
Giant digital fibrokeratoma, nail like changes, benign growth, surgical excision. Acquired digital fibrokeratoma is an uncommon, benign fibrous tumour that usually occurs in adults as a solitary lesion with a typical size of less than 1 cm. A 48-year-old Afro-Caribbean man presented to our foot and ankle clinic with a long-standing growth over the plantar aspect of the distal phalanx of the left great toe. The growth was painful and affected the patient’s mobility. It had gradually increased in size over a period of 17 years. The growth was completely excised, and the base was allowed to heal by secondary intention. The skin eventually healed, and the patient had a good outcome. The histological results confirmed that the growth was a digital fibrokeratoma. This case is of interest because of the rarity of digital fibrokeratoma and the unique morphological appearance of the tumor in this case. Additionally, we emphasise the importance of ruling out other causes of abnormal growths and considering fibrokeratoma during differential diagnoses.