Li Janet Y, Berger Michael F, Marghoob Ashfaq, Bhanot Umesh K, Toyohara Jennifer P, Pulitzer Melissa P
Department of Medicine, Dermatology Service, Memorial Sloan-Kettering Cancer Center, New York, NY, USA.
J Cutan Pathol. 2014 Aug;41(8):663-71. doi: 10.1111/cup.12339. Epub 2014 Jul 9.
Phacomatosis pigmentokeratotica (PPK) is characterized by the co-existence of epidermal nevi and large segmental speckled lentiginous nevi of the papulosa type. PPK, previously explained as 'twin spot' mosaicism due to the postzygotic crossing-over of two homozygous recessive mutations, has recently been shown to derive from one postzygotic activating RAS mutation. Epidermal nevi, including those in PPK, are known to give rise to neoplasms such as trichoblastoma and basal cell carcinoma. Within speckled lentiginous nevi, Spitz nevi and melanoma have been well documented. We report a case of PPK with a combined melanocytic and adnexal neoplasm presenting where the nevi conjoined. Using next-generation sequencing techniques, we were able to identify the same HRAS G13R mutation within both components of the tumor, and to show the absence of additional mutated modifier genes in a panel of 300 cancer-related genes. Given the genetic findings in this rare tumor-type, we suggest that this case may be used as a model for understanding the development of biphenotypic neoplasia or intratumoral heterogeneity in some cases.
色素角化性错构瘤病(PPK)的特征是表皮痣与丘疹型大片段斑点状雀斑样痣并存。PPK以前被解释为由于两个纯合隐性突变的合子后交叉而形成的“双斑”镶嵌现象,最近研究表明它源自一个合子后激活的RAS突变。已知包括PPK中的表皮痣会引发肿瘤,如毛母细胞瘤和基底细胞癌。在斑点状雀斑样痣中,已充分记录到斯皮茨痣和黑色素瘤。我们报告了1例PPK病例,在痣相连处出现了黑素细胞和附属器肿瘤合并的情况。使用下一代测序技术,我们能够在肿瘤的两个成分中鉴定出相同的HRAS G13R突变,并在一组300个癌症相关基因中显示没有其他突变的修饰基因。鉴于这种罕见肿瘤类型的基因研究结果,我们认为该病例可作为理解某些情况下双表型肿瘤形成或肿瘤内异质性发展的模型。