Thornton Sharon Longshore, Reid Janet, Papay Francis A, Vidimos Allison T
Division of Dermatologic Surgery, Department of Dermatology, Cleveland Clinic Foundation, Cleveland, Ohio 44195, USA.
J Am Acad Dermatol. 2005 Jul;53(1):76-83. doi: 10.1016/j.jaad.2004.11.071.
Dermatofibrosarcoma protuberans (DFSP) is especially challenging to recognize and diagnose in children. Prompt and definitive treatment is essential based on the tumor's high rate of recurrence. Our purpose is to increase physician awareness and recognition of DFSP in the pediatric population with the largest case series of childhood DFSP to our knowledge thus reported in the literature. We also propose that magnetic resonance imaging (MRI) may be useful in the preoperative assessment. The records of 10 patients with primary DFSP between the ages of 8 months and 16 years were reviewed. Only 1 of 10 patients was given the correct diagnosis at the initial medical evaluation. Of the 10 cases, 5 were congenital. The average delay in diagnosis was 5 years. Of the patients, 5 had preoperative MRI to delineate the size and extent of the tumor. In the two cases with the largest tumors preoperative MRI significantly altered surgical planning and execution. Thus, preoperative MRI may be helpful in planning for successful surgical clearance of large tumors and preventing local recurrence. All 10 cases were treated with Mohs micrographic surgery and no recurrences were noted with a follow-up range of 6 weeks to 17 years.
隆突性皮肤纤维肉瘤(DFSP)在儿童中尤其难以识别和诊断。鉴于该肿瘤的高复发率,及时且明确的治疗至关重要。据我们所知,本文报告了最大规模的儿童DFSP病例系列,目的是提高医生对儿科人群中DFSP的认识和识别能力。我们还提出,磁共振成像(MRI)可能有助于术前评估。回顾了10例年龄在8个月至16岁之间的原发性DFSP患者的病历。10例患者中只有1例在初次医学评估时得到了正确诊断。10例病例中,5例为先天性。平均诊断延迟为5年。患者中有5例行术前MRI以明确肿瘤的大小和范围。在肿瘤最大的两例病例中,术前MRI显著改变了手术规划和实施。因此,术前MRI可能有助于规划成功切除大肿瘤并预防局部复发。所有10例病例均接受了莫氏显微外科手术治疗,随访时间为6周至17年,未发现复发。