| Literature DB >> 18844942 |
Mizuo Ando1, Yukihiro Nakanishi, Masao Asai, Akiko Maeshima, Yoshihiro Matsuno.
Abstract
Mucoepidermoid carcinoma of the thyroid gland is a rare tumor first described by Rhatigan et al. in 1977. Its pathogenesis is still controversial. With regard to its most likely origin, some authors have suggested that it arises directly from follicular epithelium whereas others have proposed that it arises from ultimobranchial body (diverticulum from the fourth pharyngeal pouch) remnants, also known as solid cell nests (SCN). Herein is reported a unique case of thyroid mucoepidermoid carcinoma. The patient, a 67-year-old man, presented with a non-tender thyroid mass and vocal cord fixation. The tumor was poorly defined, necessitating subtotal thyroidectomy with composite resection of the adjacent structures. Pathologically, the tumor cells had characteristics of mucoepidermoid carcinoma, along with layers of columnar cells showing marked ciliation resembling respiratory-type epithelium, suggesting that this rare tumor had originated from SCN. p63 immunopositivity in the tumor provided additional evidence for the pathogenesis.Entities:
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Year: 2008 PMID: 18844942 DOI: 10.1111/j.1440-1827.2008.02303.x
Source DB: PubMed Journal: Pathol Int ISSN: 1320-5463 Impact factor: 2.534