Your browser doesn't support javascript.
loading
Squamoid Eccrine Ductal Carcinoma Displays Ultraviolet Mutations and Intermediate Gene Expression Relative to Squamous Cell Carcinoma, Microcystic Adnexal Carcinoma, and Porocarcinoma.
Harms, Paul W; Runge, Mason; Chan, May P; Liu, Chia-Jen; Qin, Zhaoping; Worden, Francis; Robinson, Dan R; Chinnaiyan, Arul M; Mclean, Scott A; Harms, Kelly L; Fullen, Douglas R; Patel, Rajiv M; Andea, Aleodor A; Udager, Aaron M.
Afiliação
  • Harms PW; Department of Pathology, University of Michigan Medical School, Ann Arbor, Michigan; Department of Dermatology, University of Michigan Medical School, Ann Arbor, Michigan; Rogel Comprehensive Cancer Center, University of Michigan Medical School, Ann Arbor, Michigan; Michigan Center for Translational
  • Runge M; Department of Dermatology, University of Michigan Medical School, Ann Arbor, Michigan.
  • Chan MP; Department of Pathology, University of Michigan Medical School, Ann Arbor, Michigan; Department of Dermatology, University of Michigan Medical School, Ann Arbor, Michigan.
  • Liu CJ; Department of Pathology, University of Michigan Medical School, Ann Arbor, Michigan; Michigan Center for Translational Pathology, University of Michigan Medical School, Ann Arbor, Michigan.
  • Qin Z; Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, Michigan.
  • Worden F; Rogel Comprehensive Cancer Center, University of Michigan Medical School, Ann Arbor, Michigan; Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, Michigan.
  • Robinson DR; Department of Pathology, University of Michigan Medical School, Ann Arbor, Michigan; Michigan Center for Translational Pathology, University of Michigan Medical School, Ann Arbor, Michigan.
  • Chinnaiyan AM; Department of Pathology, University of Michigan Medical School, Ann Arbor, Michigan; Rogel Comprehensive Cancer Center, University of Michigan Medical School, Ann Arbor, Michigan; Michigan Center for Translational Pathology, University of Michigan Medical School, Ann Arbor, Michigan; Howard Hughes M
  • Mclean SA; Department of Otolaryngology-Head and Neck Surgery, University of Michigan, Ann Arbor, Michigan.
  • Harms KL; Department of Dermatology, University of Michigan Medical School, Ann Arbor, Michigan.
  • Fullen DR; Department of Pathology, University of Michigan Medical School, Ann Arbor, Michigan; Department of Dermatology, University of Michigan Medical School, Ann Arbor, Michigan.
  • Patel RM; Department of Pathology, University of Michigan Medical School, Ann Arbor, Michigan; Department of Dermatology, University of Michigan Medical School, Ann Arbor, Michigan; Cutaneous Pathology, WCP Laboratories, Inc, Maryland Heights, Missouri.
  • Andea AA; Department of Pathology, University of Michigan Medical School, Ann Arbor, Michigan; Department of Dermatology, University of Michigan Medical School, Ann Arbor, Michigan; Roswell Park Comprehensive Cancer Center, Buffalo, New York, New York.
  • Udager AM; Department of Pathology, University of Michigan Medical School, Ann Arbor, Michigan; Rogel Comprehensive Cancer Center, University of Michigan Medical School, Ann Arbor, Michigan; Michigan Center for Translational Pathology, University of Michigan Medical School, Ann Arbor, Michigan.
Mod Pathol ; 37(11): 100592, 2024 Aug 21.
Article em En | MEDLINE | ID: mdl-39154783
ABSTRACT
Squamoid eccrine ductal carcinoma is a rare infiltrative tumor with morphologic features intermediate between squamous cell carcinoma (SCC) and sweat gland carcinomas such as microcystic adnexal carcinoma. Although currently classified as a sweat gland carcinoma, it has been debated whether squamoid eccrine ductal carcinoma is better classified as a variant of SCC. Furthermore, therapeutic options for patients with advanced disease are lacking. Here, we describe clinicopathologic features of a cohort of 15 squamoid eccrine ductal carcinomas from 14 unique patients, with next-generation sequencing DNA profiling for 12 cases. UV signature mutations were the dominant signature in the majority of cases. TP53 mutations were the most highly recurrent specific gene alteration, followed by mutations in NOTCH genes. Recurrent mutations in driver oncogenes were not identified. By unsupervised comparison of global transcriptome profiles in squamoid eccrine ductal carcinoma (n = 7) to SCC (n = 10), porocarcinoma (n = 4), and microcystic adnexal carcinoma (n = 4), squamoid eccrine ductal carcinomas displayed an intermediate phenotype between SCC and sweat gland tumors. Squamoid eccrine ductal carcinoma displayed significantly higher expression of 364 genes (including certain eccrine markers) and significantly lower expression of 525 genes compared with other groups. Our findings support the classification of squamoid eccrine ductal carcinoma as a carcinoma with intermediate features between SCC and sweat gland carcinoma.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article