Melanoma Unit, Department of Dermatology, Hospital Clinic Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), University of Barcelona, Centro de Investigacion Biomedica en red de enfermedades raras (CIBERER), Barcelona, Spain; Dermatology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Dermatology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York; Sheba Medical Center and Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
J Am Acad Dermatol. 2018 Feb;78(2):278-288. doi: 10.1016/j.jaad.2017.09.065. Epub 2017 Oct 9.
Knowledge regarding the morphologic spectrum of pediatric melanoma (PM) is sparse, and this may in part contribute to delay in detection and thicker tumors.
To analyze the clinicodermoscopic characteristics of PM.
Retrospective study of 52 melanomas diagnosed in patients before the age of 20 years.
On the basis of its clinical, dermoscopic, and histopathologic characteristics, PM can be classified as spitzoid or nonspitzoid. The nonspitzoid melanomas (n = 37 [72.3%]) presented in patients with a mean age of 16.3 years (range, 8-20) and were associated with a high-risk phenotype and a pre-existing nevus (62.2%). The spitzoid melanomas (n = 15 [27.7%]) were diagnosed in patients at a mean age of 12.5 years (range, 2-19) and were mostly de novo lesions (73.3%) located on the limbs (73.3%). Whereas less than 25% of PMs fulfilled the modified clinical ABCD criteria (amelanotic, bleeding bump, color uniformity, de novo at any diameter), 40% of spitzoid melanomas did. Dermoscopic melanoma criteria were found in all cases. Nonspitzoid melanomas tended to be multicomponent (58.3%) or have nevus-like (25%) dermoscopic patterns. Spitzoid melanomas revealed atypical vascular patterns with shiny white lines (46.2%) or an atypical pigmented spitzoid pattern (30.8%). There was good correlation between spitzoid subtype histopathologically and dermoscopically (κ = 0.66).
A retrospective study without re-review of pathologic findings.
Dermoscopy in addition to conventional and modified clinical ABCD criteria helps in detecting PM. Dermoscopy assists in differentiating spitzoid from nonspitzoid melanomas.
儿科黑色素瘤(PM)的形态学谱知识有限,这在一定程度上可能导致检测延迟和肿瘤变厚。
分析 PM 的临床皮肤镜特征。
回顾性研究 52 例年龄在 20 岁以下的患者诊断为黑色素瘤。
根据其临床、皮肤镜和组织病理学特征,PM 可分为 Spitz 型或非 Spitz 型。非 Spitz 型黑色素瘤(n=37[72.3%])患者的平均年龄为 16.3 岁(范围为 8-20 岁),与高危表型和先前存在的痣(62.2%)相关。Spitz 型黑色素瘤(n=15[27.7%])在平均年龄为 12.5 岁(范围为 2-19 岁)的患者中诊断,大多为新发病变(73.3%)位于四肢(73.3%)。虽然不到 25%的 PM 符合改良的临床 ABCD 标准(无色素、出血性肿块、颜色均匀、任何直径的新发病变),但 40%的 Spitz 型黑色素瘤符合。所有病例均发现皮肤镜黑色素瘤标准。非 Spitz 型黑色素瘤倾向于多成分(58.3%)或具有痣样(25%)皮肤镜模式。Spitz 型黑色素瘤显示出典型的血管模式,有闪亮的白线(46.2%)或非典型色素性 Spitz 型模式(30.8%)。组织病理学上 Spitz 亚型与皮肤镜下具有良好的相关性(κ=0.66)。
无病理发现再复查的回顾性研究。
除了传统和改良的临床 ABCD 标准外,皮肤镜检查有助于检测 PM。皮肤镜有助于区分 Spitz 型和非 Spitz 型黑色素瘤。