Spinelli Claudio, Rallo Leonardo, Morganti Riccardo, Mazzotti Valentina, Inserra Alessandro, Cecchetto Giovanni, Massimino Maura, Collini Paola, Strambi Silvia
Pediatric and Adolescent Surgery Division, University of Pisa, Italy.
Pediatric and Adolescent Surgery Division, University of Pisa, Italy.
J Pediatr Surg. 2019 Mar;54(3):521-526. doi: 10.1016/j.jpedsurg.2018.05.017. Epub 2018 May 29.
BACKGROUND/PURPOSE: The purpose of the study is to describe the anatomoclinical, diagnostic, therapeutic and prognostic aspects of pediatric follicular thyroid carcinoma (FTC) in order to choose the best therapeutic strategy.
Our study includes patients ≤18 years old surgically treated for FTC in four Italian Pediatric Surgery Centers from January 2000 to March 2017. The collected data were compared with those of 132 patients matched for age with a histological diagnosis of papillary thyroid carcinoma (PTC) surgically treated in the same institutions during the same period and with the data of patients diagnosed with FTC found in the literature; p-values <0.05 were considered significant.
21 (70%) of the 30 patients with a histological diagnosis of FTC underwent hemithyroidectomy while 9 (30%) underwent total thyroidectomy. 11 (55%) out of 21 patients were subjected to a completion of thyroidectomy. All patients are alive (OS = 100%) without recurrence or relapse of the disease. Compared with PTC, FTC is significant for capsule infiltration (p < 0.0001), vascular invasion (p = 0.0014) and T-stage T3-T4 (p = 0.013). However, multifocality (p < 0.001), extrathyroid extension (p < 0.0001) and lymph node metastasis (p < 0.0001) are more evident in PTC.
The conservative approach seems to be a valid surgical treatment for pediatric patients diagnosed with MI-FTC. For patients with wide vascular invasion and/or a tumor >4 cm, especially with high after-surgery Tg rate, a completion of thyroidectomy is recommended. In patients with multifocal neoplasia, and/or tumor size ≥4 cm, and/or extrathyroid extension, and/or lymph node metastasis, and/or distant metastasis, total thyroidectomy followed by radioiodine therapy is generally indicated.
II.
背景/目的:本研究旨在描述儿童滤泡性甲状腺癌(FTC)的解剖临床、诊断、治疗及预后情况,以便选择最佳治疗策略。
我们的研究纳入了2000年1月至2017年3月期间在意大利四个儿科手术中心接受FTC手术治疗的18岁及以下患者。将收集的数据与同期在同一机构接受手术治疗且组织学诊断为乳头状甲状腺癌(PTC)的132名年龄匹配患者的数据以及文献中诊断为FTC的患者数据进行比较;p值<0.05被认为具有统计学意义。
30例组织学诊断为FTC的患者中,21例(70%)接受了甲状腺半叶切除术,9例(30%)接受了甲状腺全切除术。21例患者中有11例(55%)接受了甲状腺补充切除术。所有患者均存活(总生存率=100%),无疾病复发或转移。与PTC相比,FTC在包膜浸润(p<0.0001)、血管侵犯(p=0.0014)和T分期T3-T4(p=0.013)方面具有统计学意义。然而,PTC的多灶性(p<0.001)、甲状腺外扩展(p<0.0001)和淋巴结转移(p<0.0001)更为明显。
对于诊断为微小浸润性FTC的儿童患者,保守手术似乎是一种有效的治疗方法。对于血管侵犯广泛和/或肿瘤>4cm,尤其是术后Tg水平较高的患者,建议进行甲状腺补充切除术。对于有多灶性肿瘤、和/或肿瘤大小≥4cm、和/或甲状腺外扩展和/或淋巴结转移和/或远处转移的患者,一般建议行甲状腺全切除术,随后进行放射性碘治疗。
II级。