Atypical Spitz tumors in patients younger than 18 years

作者:Massi Daniela*; Tomasini Carlo; Senetta Rebecca; Paglierani Milena; Salvianti Francesca; Errico Maria Elena; Donofrio Vittoria; Collini Paola; Tragni Gabrina; Sementa Angela Rita; Rongioletti Franco; Boldrini Renata; Ferrari Andrea; Gambini Claudio; Montesco Maria Cristina
来源:Journal of the American Academy of Dermatology, 2015, 72(1): 37-46.
DOI:10.1016/j.jaad.2014.09.049

摘要

Background: Diagnosis and proper management of atypical Spitz tumors in pediatric age are still controversial. Objective: We sought to investigate the clinicopathological and molecular features of atypical Spitz tumors in patients aged 18 years or younger. Methods: We performed a retrospective clinicopathological and fluorescence in situ hybridization study on 50 pediatric atypical Spitz tumors. Results: Parameters that were significantly correlated with a diagnosis of atypical Spitz tumors over Spitz nevus included asymmetry, level IV/V, lack of maturation, solid growth, nuclear pleomorphism, high nuclear-cytoplasmic ratio, atypical and deep mitoses, and more than 6 mitoses/mm(2). In the atypical Spitz tumors group, a significantly higher mitotic rate was observed in prepuberal age (P = .04). The 4-probe fluorescence in situ hybridization melanoma assay did not discriminate atypical Spitz tumors from Spitz nevi. Heterozygous 9p21 loss was found in 3 of 37 cases and homozygous 9p21 loss in 2 of 37 cases. Only 1 child experienced a fatal outcome, showing genetic abnormalities by melanoma fluorescence in situ hybridization probe and a heterozygous 9p21 deletion. Limitations: The limited number of adverse outcomes did not allow the prognostic analysis of single morphologic features. Conclusion: Pediatric atypical Spitz tumors are associated with minimal lethal potential. Atypical Spitz tumors require complete excision and careful follow-up while our data do not support any clinical benefit for the sentinel lymph node biopsy procedure and completion lymphadenectomy.

  • 出版日期2015-1