Nakamura T, Moriyama S, Nariya S, Sano K, Shirota H, Kato R
Department of Pathology, Suwa Red Cross Hospital, Japan.
Pathol Int. 1998 Jun;48(6):467-70. doi: 10.1111/j.1440-1827.1998.tb03934.x.
A rare case of a macrofollicular variant of papillary thyroid carcinoma occurring in an 18-year-old male is described. The extirpated tumor, 5.5 x 5.5 x 3.5 cm in size, was well demarcated and multinodular, and histopathologically showed a predominantly macrofollicular structure reminiscent of adenomatous goiter or macrofollicular adenoma. In the tumor tissue, however, there were several small foci of microfollicular or papillary structure with the nuclei characteristic of papillary carcinoma. Parts of the macrofollicular areas also showed similar nuclear characteristics with a transition to microfollicular or papillary areas. Incomplete capsular invasion and minimal vascular invasion were also present. Additional resected specimens contained small metastatic nodules in the residual left lobe and lymph nodes. Immunohistochemistry showed a small number of p53-positive tumor cells in the microfollicular or papillary areas. It is suggested that this tumor is a well-differentiated variant which should be distinguished from benign thyroid lesions, although there have been some cases of metastases which appear related to capsular and/or vascular invasion.
本文描述了一例罕见的18岁男性甲状腺乳头状癌大滤泡变异型病例。切除的肿瘤大小为5.5×5.5×3.5 cm,边界清晰,呈多结节状,组织病理学显示主要为大滤泡结构,类似腺瘤样甲状腺肿或大滤泡性腺瘤。然而,在肿瘤组织中,有几个小灶呈微滤泡或乳头状结构,具有乳头状癌的核特征。部分大滤泡区域也显示出类似的核特征,并向微滤泡或乳头状区域过渡。还存在不完全的包膜侵犯和微小的血管侵犯。额外切除的标本在残留的左叶和淋巴结中含有小转移结节。免疫组化显示微滤泡或乳头状区域有少量p53阳性肿瘤细胞。提示该肿瘤是一种高分化变异型,应与良性甲状腺病变相鉴别,尽管已有一些转移病例似乎与包膜和/或血管侵犯有关。