Haba R, Miki H, Kobayashi S, Kushida Y, Saoo K, Hirakawa E, Ohmori M
First Department of Pathology, Kagawa Medical School, Kagawa, Japan.
Pathol Int. 2000 Nov;50(11):897-900. doi: 10.1046/j.1440-1827.2000.01130.x.
An extremely rare case of intrathyroidal branchial cleft-like cyst is reported. A 71-year-old man complained of a growing mass in the right lateral neck. A cystic mass in the upper lobe of the right thyroid was demonstrated by ultrasonography and computed tomography. The surgical specimen revealed a cystic mass with dense fibrous capsule, 22 x 20 x 10 mm in size. Microscopically, the cyst walls and the surrounding thyroid tissue contained severe lymphoid cell infiltration with lymphoid follicle. Squamous epithelium lined the cyst wall. Immunohistochemically, squamous epithelium was positive for keratin, cytokeratin 19, carcinoembryonic antigen, and epithelial membrane antigen, but negative for calcitonin and chromogranin A. The patient is currently well with no evidence or recurrence for 43 months.
报道了1例极其罕见的甲状腺内鳃裂样囊肿病例。一名71岁男性主诉右侧颈部肿物逐渐增大。超声及计算机断层扫描显示右叶甲状腺上极有一囊性肿物。手术标本为一大小22×20×10mm、有致密纤维包膜的囊性肿物。显微镜下,囊肿壁及周围甲状腺组织有严重的淋巴细胞浸润及淋巴滤泡。囊肿壁内衬鳞状上皮。免疫组化显示,鳞状上皮对角蛋白、细胞角蛋白19、癌胚抗原及上皮膜抗原呈阳性,但对降钙素及嗜铬粒蛋白A呈阴性。该患者目前情况良好,43个月无复发迹象。