Ando K, Goto Y, Hirabayashi N, Matsumoto Y, Ohashi M
Department of Dermatology, Nagoya First Red Cross Hospital, Japan.
Dermatol Surg. 1995 Apr;21(4):339-41. doi: 10.1111/j.1524-4725.1995.tb00186.x.
Only seven cases of cartilaginous tumors of the skin have been described in the dermatologic literature.
We studied the nature of cutaneous cartilaginous tumors and their clinical spectrum.
We describe a 56-year-old woman with a superficial cartilaginous tumor of the sole of the foot. The tumor appeared to be a cutaneous mass and was resected.
Histologically, the tumor extended from the dermis to the subcutaneous tissue. Despite the presence of foci of nuclear changes that suggested a malignancy, there has been no recurrence in the 3 years since its removal. Our review of previous reports indicated that this case may have been a soft tissue chondroma. And it confirmed that cutaneous cartilaginous tumors comprise a superficial soft tissue chondroma and a true cutaneous chondroma primarily located in the dermis.
Our case appeared to be a cutaneous cartilaginous tumor. A complete local removal is the treatment of choice.
皮肤病学文献中仅描述过7例皮肤软骨肿瘤。
我们研究了皮肤软骨肿瘤的性质及其临床谱。
我们描述了一名56岁女性，其足底有一个浅表软骨肿瘤。该肿瘤表现为皮肤肿物并被切除。
组织学上，肿瘤从真皮延伸至皮下组织。尽管存在提示恶性的核变化灶，但自切除后3年未复发。我们对既往报告的回顾表明，该病例可能是软组织软骨瘤。并且证实皮肤软骨肿瘤包括浅表软组织软骨瘤和主要位于真皮的真性皮肤软骨瘤。
我们的病例似乎是皮肤软骨肿瘤。完整的局部切除是首选治疗方法。
