Cavallaro G, Polistena A, Fornari F, Ruperto M, Letizia C, De Toma G
Università degli Studi di Roma "La Sapienza" Policlinico Umberto I Dipartmento di Chirurgia "P. Valdoni", Italy.
G Chir. 2006 Aug-Sep;27(8-9):315-7.
Amyloid goiter is a rare pathology due to massive amyloid infiltration of thyroid tissue, which cause diffuse or localized enlargement of the gland. It can be totally asymptomatic or cause only non-specific symptoms (compression of adjacent structures, tracheal deviation). Thyroid disfunction (hypothyroidism or hyperthyroidism) is rare. It is important to differentiate primitive amyloid goiter from other kinds of amyloid infiltration of the thyroid, such as in systemic amyloidosis. The correct diagnosis can be difficult because of the common presence of amyloid in thyroid neoplasms, such as medullary thyroid carcinoma (MTC). The Authors present a case of primitive amyloid goiter, that needed immunohistochemical analysis for a correct diagnosis, and a review of the concerning literature.
淀粉样变甲状腺肿是一种罕见的病理情况,由于甲状腺组织大量淀粉样物质浸润,导致腺体弥漫性或局限性肿大。它可以完全无症状,或仅引起非特异性症状(压迫相邻结构、气管移位)。甲状腺功能障碍(甲状腺功能减退或亢进)较为罕见。将原发性淀粉样变甲状腺肿与甲状腺的其他淀粉样物质浸润类型,如系统性淀粉样变性相鉴别很重要。由于甲状腺肿瘤(如甲状腺髓样癌,MTC)中普遍存在淀粉样物质,正确诊断可能会很困难。作者报告了一例原发性淀粉样变甲状腺肿病例,该病例需要免疫组织化学分析以明确诊断,并对相关文献进行了综述。