A Case of Squamous Cell Carcinoma of the Thyroid Gland

갑상선 편평 세포암 1예

  • Roh Jin-Woo (Department of Surgery, College of Medicine, Yeung Nam University) ;
  • Lee Sang-Choon (Department of Surgery, College of Medicine, Yeung Nam University) ;
  • Lee Soo-Jung (Department of Surgery, College of Medicine, Yeung Nam University) ;
  • Kwun Koing-Bo (Department of Surgery, College of Medicine, Yeung Nam University) ;
  • Nam Hae-Joo (Department of Anatomical Pathology, College of Medicine, Yeung Nam University)
  • 노진우 (영남대학교 의과대학 일반외과학교실) ;
  • 이상춘 (영남대학교 의과대학 일반외과학교실) ;
  • 이수정 (영남대학교 의과대학 일반외과학교실) ;
  • 권굉보 (영남대학교 의과대학 일반외과학교실) ;
  • 남해주 (영남대학교 의과대학 병리학교실)
  • Published : 1990.11.01

Abstract

Squamous cell carcinoma of the thyroid gland is an extremely rare primary neoplasm, comprising only 1.1% of all primary thyroid cancers. The cancer is characterized by rapidly progressive clinical course in spite of its differentiated morphologic feature. Histogenetic origin of the cancer has also been debated. In most cases, a squamous epithelium is believed to be a result of metaplasia of a follicullar epithelium, although in rare exceptions, it can originate from a remnant of the thyroglossal duct or ultimobrachial body. Squamous cell carcinoma of the thyroid can occur in a pure form or mixed with adenocarcinoma; the latter may be designated as adenoacanthoma. Because this lesion typically runs a fulminant course, radical surgical resection at the earliest opportunity offers the best hope for cure. The lesions are usually radioresistant, and chemotherapy has not been shown to alter the course of this disease. We experienced a case of squamous carcinoma of the thyroid. This report summarize our experience and review of the literatures.

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