Wu Yi-Lei, Ting Wei-Hsin, Wey Shiuan-Li, Chen Chi-Kuan, Huang Chi-Yu, Cheng Shih-Ping, Lees Yann-Jinn
Department of Pediatrics, Mackay Memorial Hospital, Taipei, Taiwan.
J Pediatr Endocrinol Metab. 2011;24(9-10):783-6.
Poorly differentiated thyroid carcinoma (PDTC) is a rare disease with a poor prognosis in children. We describe a 9-year-old boy with a thyroid nodule composed of cystic and solid components, which became completely solid and hypoechoic and was subsequently proved to be PDTC. The tumor consisted of small- to intermediate-size round cells in a trabecular or insular pattern with hyperchromatic nuclei and mitotic figures. The tumor cells were positive for thyroid transcription factor 1 and thyroglobulin. PDTC is morphologically and prognostically between the well-differentiated and anaplastic carcinomas. It must be distinguished from the solid variant of papillary carcinoma and well-differentiated follicular carcinoma with a predominantly solid/trabecular growth pattern. The tumor stage was T2N0M0. The patient was treated with total thyroidectomy, left-sided neck level VI lymph node dissection, recombinant human thyrotropin-stimulated 131I ablation therapy, and thyroid-stimulating hormone suppression. Malignancy should be suspected in a cystic thyroid nodule that becomes solid and hypoechoic.
低分化甲状腺癌(PDTC)在儿童中是一种罕见疾病,预后较差。我们描述了一名9岁男孩,其甲状腺结节由囊性和实性成分组成,后来完全变为实性且低回声,随后被证实为PDTC。肿瘤由小至中等大小的圆形细胞构成,呈小梁状或岛状排列,细胞核深染且有核分裂象。肿瘤细胞甲状腺转录因子1和甲状腺球蛋白呈阳性。PDTC在形态学和预后方面介于高分化癌和未分化癌之间。它必须与主要呈实性/小梁状生长模式的乳头状癌实性变体以及高分化滤泡癌相鉴别。肿瘤分期为T2N0M0。患者接受了甲状腺全切术、左侧颈部VI区淋巴结清扫术、重组人促甲状腺素刺激的131I消融治疗以及促甲状腺激素抑制治疗。对于变为实性且低回声的甲状腺囊性结节应怀疑有恶性病变。