| Literature DB >> 16361718 |
Hiromi Shibuya1, Aiko Kato, Nobutaka Kai, Sakuhei Fujiwara, Makoto Goto.
Abstract
Three primary lesions of malignant melanoma developed in a 44-year-old Japanese woman with Werner syndrome. One lesion was on the right large pudental lip and the others in distinct locations on her left sole. After the wide local excision of these tumors, the wound of the large pudental lip was sutured, and the defects on the sole were covered with skin grafts. After one course of chemotherapy consisting of dacarbazine, nimustine, vincristine sulfate and local injection of Interferon beta were performed, severe myelosupression occurred and continued for two months. Defective production of WRN protein was confirmed by Western blotting, although the three representative mutations in Japanese patients, mutations 1, 4 and 6, which include over 90% of the Japanese patients, were not detected. We also reviewed 26 cases of malignant melanoma associated with Werner syndrome (WS), including ours.Entities:
Mesh:
Year: 2005 PMID: 16361718 DOI: 10.1111/j.1346-8138.2005.tb00835.x
Source DB: PubMed Journal: J Dermatol ISSN: 0385-2407 Impact factor: 4.005