McInnis-Smith Kerri M, Asamoah Eucabeth M, Demer Addison M, Sharma Kannan, Yu Caroline Y, Bradley Elizabeth A, Tooley Andrea A, Wagner Lilly H
Department of Ophthalmology.
Department of Dermatology.
Ophthalmic Plast Reconstr Surg. 2025;41(1):78-83. doi: 10.1097/IOP.0000000000002729. Epub 2024 Jun 17.
Mohs micrographic surgery with immunohistochemistry allows for same-day comprehensive margin assessment of melanoma in situ prior to subspecialty reconstruction. This study describes the oncologic and reconstructive outcomes of eyelid and periorbital melanoma in situ and identifies risk factors for complex reconstructive demands.
Retrospective case series of all patients treated with Mohs micrographic surgery with immunohistochemistry for melanoma in situ affecting the eyelids or periorbital region from 2008 to 2018 at a single institution. Tumors were assigned to the eyelid group if the clinically visible tumor involved the skin inside the orbital rim. Reconstructive variables were compared between the eyelid and periorbital cohorts.
There were 24 eyelid and 141 periorbital tumors included. The initial surgical margin for all tumors was 5.34 ± 1.54 mm and multiple Mohs stages were required in 24.2% of cases. Eyelid tumors included more recurrences ( p = 0.003), and the average defect size was larger (14.0 ± 13.3 cm 2 vs. 7.7 ± 5.4 cm 2 , p = 0.03). Risk factors for complex reconstruction included: initial tumor diameter >2 cm (odds ratio [OR]: 3.84, 95% confidence interval [CI]: 1.95-7.57) and eyelid involved by initial tumor (OR: 4.88, 95% CI: 1.94-12.28). At an average follow-up of 4.8 years, there were no melanoma-related deaths and 1 local recurrence (0.6% recurrence rate).
Mohs micrographic surgery with immunohistochemistry achieves excellent local control rates for periocular melanoma in situ. An initial surgical margin of 5 mm is frequently insufficient to achieve clear margins. The resulting defects are large, and the complexity of reconstruction can be predicted by tumor size and clinical involvement of eyelid skin.
采用免疫组织化学的莫氏显微外科手术能够在亚专业重建前对原位黑色素瘤进行当日全面的切缘评估。本研究描述了眼睑及眶周原位黑色素瘤的肿瘤学及重建效果,并确定了复杂重建需求的危险因素。
对2008年至2018年在单一机构接受采用免疫组织化学的莫氏显微外科手术治疗的所有累及眼睑或眶周区域的原位黑色素瘤患者进行回顾性病例系列研究。如果临床上可见的肿瘤累及眶缘内的皮肤,则将肿瘤归入眼睑组。比较眼睑组和眶周组之间重建相关变量。
共纳入24例眼睑肿瘤和141例眶周肿瘤。所有肿瘤的初始手术切缘为5.34±1.54mm,24.2%的病例需要多个莫氏分期。眼睑肿瘤复发更多(p = 0.003),平均缺损面积更大(14.0±13.3cm²对7.7±5.4cm²,p = 0.03)。复杂重建的危险因素包括:初始肿瘤直径>2cm(比值比[OR]:3.84,95%置信区间[CI]:1.95 - 7.57)和初始肿瘤累及眼睑(OR:4.88,95%CI:1.94 - 12.28)。平均随访4.8年,无黑色素瘤相关死亡,1例局部复发(复发率0.6%)。
采用免疫组织化学的莫氏显微外科手术对眼周原位黑色素瘤实现了出色的局部控制率。5mm的初始手术切缘常常不足以获得切缘阴性。由此产生的缺损较大,重建的复杂性可通过肿瘤大小和眼睑皮肤的临床累及情况来预测。