Fujito Hikaru, Yamanaka Hiroki, Tsuge Itaru, Katsube Motoki, Sakamoto Michiharu, Fujimoto Masakazu, Morimoto Naoki
Department of Plastic and Reconstructive Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Department of Pathology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Plast Reconstr Surg Glob Open. 2021 May 25;9(5):e3600. doi: 10.1097/GOX.0000000000003600. eCollection 2021 May.
Curettage is common in the treatment of a giant congenital melanocytic nevus (GCMN) in infants and should generally be performed before 6 months of age. Post-curettage retarded epithelialization often interferes with the ability to perform multiple operations within a short interval, and thus, it is difficult to treat large lesions in the neonatal period. We herein report a case of a GCMN comprising 20% of the total body surface area, which required multi-stage curettage, in which a cultured epithelial autograft was used to promote epithelialization of the post-curettage wound. The patient was a 1-month-old boy with a GCMN in his head, neck, chest, back, buttock, left upper arm, and a few satellite lesions. A four-stage operation was performed between 3 and 6 months of age; the cultured epithelial autograft took well after each operation, and complete epithelialization was observed at postoperative days 20, 23, 27, and 12, respectively. Seven months after the last surgery, hypertrophic scar formation was only observed in a small area of the left upper arm without axillary contracture. The color of the treated area improved, except for slight partial re-pigmentation. A skin biopsy was obtained from the re-pigmented area. The results demonstrated that nevus cells remained in the basal layer of the epidermis, hair follicles, and deep layer of the remaining dermis, suggesting that the recurrent nevus cells in the regenerated epidermis migrated from hair follicles. We conclude that the combination of curettage and the application of a cultured epithelial autograft is a promising option for GCMN treatment.
刮除术在婴儿巨大先天性黑素细胞痣(GCMN)的治疗中很常见,通常应在6个月龄前进行。刮除术后上皮化延迟常常会妨碍在短时间内进行多次手术的能力,因此,在新生儿期很难治疗大面积病变。我们在此报告一例占全身表面积20%的GCMN病例,该病例需要进行多阶段刮除术,术中使用培养的自体上皮移植来促进刮除术后伤口的上皮化。患者为一名1个月大的男婴,头部、颈部、胸部、背部、臀部、左上臂有GCMN,并有一些卫星病灶。在3至6个月龄期间进行了四阶段手术;每次手术后培养的自体上皮移植生长良好,分别在术后第20、23、27和12天观察到完全上皮化。最后一次手术后7个月,仅在左上臂的一小片区域观察到肥厚性瘢痕形成,无腋窝挛缩。除轻微的部分再色素沉着外,治疗区域的颜色有所改善。从再色素沉着区域取皮肤活检。结果表明,痣细胞仍存在于表皮基底层、毛囊和剩余真皮深层,提示再生表皮中复发的痣细胞从毛囊迁移而来。我们得出结论,刮除术与培养的自体上皮移植联合应用是治疗GCMN的一种有前景的选择。