Durmaz Erdem, Barsal Ebru, Parlak Mesut, Gurer Inanc, Karaguzel Gungor, Akcurin Sema, Bircan Iffet
Department of Pediatric Endocrinology, Akdeniz University, Antalya, Turkey.
J Pediatr Endocrinol Metab. 2012;25(9-10):997-1000. doi: 10.1515/jpem-2012-0207.
Ectopic intrathyroidal thymus tissue that may be present as a thyroid nodule is rarely reported. We present a case of a 4-year-old boy with a solitary thyroid nodule. Real-time thyroid ultrasound showed a calcified nodule in the right lobe. Complete blood count, serum calcitonin, and thyroglobulin concentration were normal and antithyroid antibodies were negative. Fine-needle aspiration (FNA) biopsy was revealed as inadequate for cytological examination. During his follow-up, nodular enlargement was found, and the patient was subjected to surgical total excision of the right lobe of the thyroid gland. Pathological examination showed an ectopic intrathyroidal thymus tissue. In childhood, ectopic intrathyroidal thymus tissue can present as an enlarging microcalcified thyroid nodule that may mimic thyroid cancer and may grow during follow-up.
可能表现为甲状腺结节的异位甲状腺内胸腺组织鲜有报道。我们报告一例4岁男孩,有一个孤立性甲状腺结节。实时甲状腺超声显示右叶有一个钙化结节。全血细胞计数、血清降钙素和甲状腺球蛋白浓度正常,抗甲状腺抗体阴性。细针穿刺(FNA)活检显示细胞检查不充分。在随访期间,发现结节增大,患者接受了甲状腺右叶手术全切除。病理检查显示为异位甲状腺内胸腺组织。在儿童期,异位甲状腺内胸腺组织可表现为增大的微钙化甲状腺结节,可能酷似甲状腺癌,且在随访期间可能生长。