儿童分化型甲状腺癌症肺转移的放射性碘诊断1例报告

E. H. Gadzhieva, T. Geliashvili, M. O. Goncharov, A. Pronin, A. Krylov, V. S. Ilyakov, A. V. Parnas
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引用次数: 0

摘要

儿童分化型甲状腺癌肺转移(LM)发生率为7-30%,是成人的3-4倍。LM的早期诊断提高了放射性碘治疗的效果和完全缓解率。我们提出了一个临床病例,展示了儿童LM诊断的具体特征。患者G,一名9岁男孩,因体重超标被观察了两年。甲状腺超声检查显示多发低回声结节,细胞学证实乳头状癌。胸部CT显示双肺胸膜下病灶达3mm,更符合肺内淋巴结,但不能完全排除转移性病变。于2022年1月行甲状腺切除术并中央和外侧颈部切除术。组织学检查显示整个甲状腺有多灶性乳头状癌生长,伴Tall细胞区,并转移到多个颈部淋巴结。根据TNM分级(美国癌症联合委员会(AJCC),第8版),肿瘤分级为pT2N1bM0, i期。手术治疗后7周,患者接受I-123全身扫描(注射I-123 50 MBq后24小时),并接受内源性tsh刺激放射碘治疗(停药4周)。I-123扫描(全身和SPECT/CT)未检测到碘积聚组织。然而,治疗后(给予2 GBq I-131 72小时后)显像(全身和SPECT/CT)显示甲状腺组织残留和双肺弥漫性I-131积聚。tsh刺激甲状腺球蛋白为118 ng/ml,甲状腺球蛋白抗体为21 IU/ml。肺内I-131病理性积累,甲状腺球蛋白水平升高,胸部CT表现为恶性肿瘤,肿瘤进程分期- pT2N1bM1,二期手术,计划继续放射性碘治疗。本临床病例在诊断LM时,I-123显像结果为假阴性,胸部CT扫描不确定,需要动态监测。在给予I-131治疗活性后的显像显示LM,从而改变进一步的治疗策略,继续放射性碘治疗,增加实现疾病完全缓解的可能性。与LM相关的因素是多灶性生长、颈部淋巴结肿大受累和高tsh刺激的甲状腺球蛋白水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Radioiodine diagnosis of differentiated thyroid cancer lung metastases in children: a case report
Lung metastases (LM) in differentiated thyroid cancer in children occur in 7-30% of cases, 3-4 times more often than in adults. Early diagnosis of LM improves the results of radioiodine therapy and the rate of complete remissions. We present a clinical case demonstrating the specific features of LM diagnosis in children. Patient G., a 9-year-old boy, was for two years observed for excessive body weight. Ultrasound thyroid gland examination revealed multiple hypoechogenic nodules, cytologically verified papillary cancer. Computed tomography (CT) of the chest revealed subpleural foci up to 3 mm in both lungs, which were more consistent with intrapulmonary lymph nodes, but did not completely rule out metastatic lesions. A thyroidectomy with central and lateral neck dissections was performed in January 2022. Histologic examination revealed multifocal papillary cancer growth in the entire thyroid gland with Tall cell sites and metastases to multiple cervical lymph nodes. According to TNM classification (American Joint Committee on Cancer (AJCC), 8th edition), the tumor grade was considered as pT2N1bM0, stage I. Seven weeks after surgical treatment, the patient underwent whole body scintigraphy with I-123 (24 hours after I-123 injection for 50 MBq) followed by radioiodine therapy on endogenous TSH-stimulation (4 weeks of L-thyroxine withdrawal). Scintigraphy with I-123 (whole-body and SPECT/CT) did not detect iodine-accumulating tissue. However, post-therapy (72 hours after administration of 2 GBq I-131) scintigraphy (whole-body and SPECT/CT) revealed residual thyroid tissue and diffuse accumulation of I-131 in both lungs. The TSH-stimulated thyroglobulin was 118 ng/ml, and thyroglobulin antibodies were 21 IU/ml. Pathological accumulation of I-131 in the lungs in combination with the elevated thyroglobulin level and chest CT findings were regarded as LM, therefore the tumor process was restaged — pT2N1bM1, stage II and radioiodine therapy was planned to continue.Conclusion. In this clinical case, when diagnosing LM, the result of scintigraphy with I-123 was false-negative, and chest CT scan was uncertain, requiring dynamic monitoring. Scintigraphy after administration of I-131 therapeutic activity revealed LM, thereby changing further treatment strategy to continued radioiodine therapy and increasing the possibility of achieving complete disease remission. Factors associated with LM were miltifocal growth, massive neck lymph node involvement and high TSH-stimulated thyroglobulin levels.
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