Kim Jin Yong, Choi Mira, Jo Seong Jin, Min Hye Sook, Cho Kwang Hyun
*Department of Dermatology, Seoul National University College of Medicine, Seoul, Korea; †Institute of Human-Environment Interface Biology, Seoul National University, Seoul, Korea; ‡Laboratory of Cutaneous Aging and Hair Research, Biomedical Research Institute, Seoul National University Hospital, Seoul, Korea; and §Department of Pathology, Seoul National University College of Medicine, Seoul, Korea.
Am J Dermatopathol. 2014 Feb;36(2):142-7. doi: 10.1097/DAD.0b013e31829bea8b.
Acral lentiginous melanoma (ALM) is the most common type of cutaneous melanoma in Asian populations. Traditionally, ALM was believed to have a poorer prognosis than other subtypes of cutaneous melanoma because of its aggressive behavior. However, in Asians, there have been several unusual case reports that have shown only subtle melanocytic proliferation despite clinically malignant manifestations. We performed a retrospective study of 13 patients with ALM. We reviewed the clinical histories, histopathologies, and immunohistochemical staining from these patients. Clinically, the lesions were characterized by a brown to black pigmented patch with irregular borders and variegated pigmentation on the sole, heel, or finger. Histopathologically, most specimens revealed only bland scattered proliferation of atypical melanocytes without marked cellular atypia or dermal invasion. However, some of the lesions were suspected to progress to the invasive stage, into the papillary dermis after a long period of time. Although cytological atypia of the melanocytes is not sufficient to ALM in situ, the melanocytic proliferation pattern, dermal inflammation, and correlation with clinical presentation would suffice in making the correct diagnosis of ALM in situ. In these cases, more biopsies of other areas should be recommended for the precise diagnosis and early complete excision in accordance with ALM in situ.
肢端雀斑样痣黑色素瘤(ALM)是亚洲人群中最常见的皮肤黑色素瘤类型。传统上,由于其侵袭性,人们认为ALM的预后比其他皮肤黑色素瘤亚型更差。然而,在亚洲人中,有几例不寻常的病例报告显示,尽管有临床恶性表现,但仅存在轻微的黑素细胞增殖。我们对13例ALM患者进行了回顾性研究。我们回顾了这些患者的临床病史、组织病理学和免疫组化染色。临床上,病变表现为棕色至黑色的色素沉着斑,边界不规则,足底、足跟或手指有斑驳色素沉着。组织病理学上,大多数标本仅显示非典型黑素细胞的平淡散在增殖,无明显细胞异型性或真皮浸润。然而,一些病变在很长一段时间后被怀疑进展到侵袭期,侵入乳头真皮。虽然黑素细胞的细胞学异型性不足以诊断原位ALM,但黑素细胞增殖模式、真皮炎症以及与临床表现的相关性足以正确诊断原位ALM。在这些病例中,应建议对其他区域进行更多活检,以便根据原位ALM进行精确诊断和早期完整切除。