Herzum Astrid, Occella Corrado, Vellone Valerio Gaetano, Gariazzo Lodovica, Pastorino Carlotta, Ferro Jacopo, Sementa Angela, Mazzocco Katia, Vercellino Nadia, Viglizzo Gianmaria
Dermatology Unit, U.O.C. Dermatologia e Centro Angiomi, IRCCS Istituto Giannina Gaslini, Via Gerolamo Gaslini, 5-16147 Genova, Italy.
Pathology Unit, U.O.C. Anatomia Patologica, IRCCS Istituto Giannina Gaslini, Via Gerolamo Gaslini, 5-16147 Genova, Italy.
Diagnostics (Basel). 2023 Jul 15;13(14):2380. doi: 10.3390/diagnostics13142380.
Spitzoid lesions are a wide tumour class comprising Spitz nevus (SN), atypical Spitz tumour (AST) and Spitz melanoma (SM).
We conducted a single-centre-based retrospective survey on all histologically diagnosed spitzoid lesions of paediatric patients (1-18 years) of the last 10 years (2012-2022). Histopathological reports and electronic records of patients were used to retrieve relevant data regarding patients' features, clinical and dermatoscopical aspects of lesions when recorded, and FISH tests when present.
Of 255 lesions, 82% were histologically benign, 17% atypical, 1% malignant. Clinically, 100% of SM were large (≥6 mm) and raised; AST were mainly large (63%), raised (98%), pink (95%). Small (≤5 mm), pigmented, flat lesions correlated with benign histology (respectively 90%, 97%, 98% SN) ( < 0.0001). Dermatoscopical patterns were analysed in 100 patients: starburst pattern correlated with benign histology (26% SN ( = 0.004)), while multicomponent pattern correlated with atypical/malignant lesions (56% AST, 50% SM ( = 0.0052)). Eighty-five lesions were subjected to fluorescence in situ hybridization (FISH): 34 (71% AST; 29% SN) were FISH-positive; 51 (63% SN; 37% AST) were FISH-negative ( = 0.0038).
This study confirmed predominant benign histology (82%) of paediatric spitzoid lesions, thus detecting 17% AST and 1% SM, highlighting the need for caution in handling spitzoid lesions.
Until AST are considered potentially malignant proliferations and no reliable criteria are identified to distinguish them, the authors suggest a prudent approach, especially in children.
Spitzoid病变是一大类肿瘤,包括Spitz痣(SN)、非典型Spitz肿瘤(AST)和Spitz黑色素瘤(SM)。
我们对过去10年(2012 - 2022年)所有组织学诊断为儿科患者(1 - 18岁)的Spitzoid病变进行了单中心回顾性调查。利用组织病理学报告和患者的电子记录来检索有关患者特征、病变的临床和皮肤镜检查方面(如有记录)以及荧光原位杂交(FISH)检测(如有)的相关数据。
在255个病变中,82%组织学上为良性,17%为非典型,1%为恶性。临床上,100%的SM较大(≥6mm)且隆起;AST主要较大(63%)、隆起(98%)、呈粉红色(95%)。小(≤5mm)、色素沉着、扁平病变与良性组织学相关(分别为90%、97%、98%的SN)(<0.0001)。对100例患者的皮肤镜模式进行了分析:星爆模式与良性组织学相关(26%的SN(P = 0.004)),而多成分模式与非典型/恶性病变相关(56%的AST,50%的SM(P = 0.0052))。85个病变进行了荧光原位杂交(FISH)检测:34个(71%的AST;29%的SN)FISH阳性;51个(63%的SN;37%的AST)FISH阴性(P = 0.0038)。
本研究证实儿科Spitzoid病变主要为良性组织学(82%),从而检测出17%的AST和1%的SM,强调了处理Spitzoid病变时需谨慎。
在AST被视为潜在恶性增殖且未确定可靠的鉴别标准之前,作者建议采取谨慎的方法,尤其是在儿童中。