Literature DB >> 15513515

A possible case of Werner syndrome presenting with multiple cancers.

Hiroyoshi Iguchi1, Masahiro Takayama, Makoto Kusuki, Kishiko Sunami, Aki Nakamura, Hideo Yamane, Yoshito Yamashita, Masaichi Ohira, Kosei Hirakawa.   

Abstract

The treatment of a man with six metachronous primary cancers is described. The primary lesions were in the soft palate, both edges of the tongue, the hard palate, the esophagus, and the right ureter. Pathologically, all of the first five tumors in the head and neck and esophagus were proven to be squamous cell carcinoma with various grades of differentiation, and the last one was transitional cell carcinoma. The cancers were found in the early clinical stage, and were completely controlled one by one except for the ureteral tumor under treatment. His characteristic medical history and physical findings, i.e. bilateral cataracts, short stature, baldness, diabetes mellitus, high-pitched voice, and multiple malignancies, met the clinical criteria for possible Werner syndrome, a genetic premature aging disorder, though the possibility of phenocopy of this syndrome has not been ruled out. We have followed him carefully because he might be vulnerable to malignant tumor formation.

Entities:  

Mesh:

Year:  2004        PMID: 15513515     DOI: 10.1080/03655230410018336

Source DB:  PubMed          Journal:  Acta Otolaryngol Suppl        ISSN: 0365-5237


  1 in total

1.  DNA repair biomarkers XPF and phospho-MAPKAP kinase 2 correlate with clinical outcome in advanced head and neck cancer.

Authors:  Tanguy Y Seiwert; XiaoZhe Wang; Jana Heitmann; Vivian Villegas-Bergazzi; Kam Sprott; Stephen Finn; Esther O'Regan; Allan D Farrow; Ralph R Weichselbaum; Mark W Lingen; Ezra E W Cohen; Kerstin Stenson; David T Weaver; Everett E Vokes
Journal:  PLoS One       Date:  2014-07-14       Impact factor: 3.240

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.