Division of Endocrinology, Boston Children's Hospital, Boston, Massachusetts.
Institutional Centers for Clinical and Translational Research, Boston Children's Hospital, Boston, Massachusetts.
J Clin Endocrinol Metab. 2018 Sep 1;103(9):3557-3565. doi: 10.1210/jc.2018-00895.
Most pediatric thyroid nodules are cytologically benign, but few data exist to guide treatment.
To describe the natural history and outcomes of cytologically benign, pediatric thyroid nodules.
Cohort study.
Multidisciplinary thyroid clinic at an academic medical center.
Consecutive pediatric patients (≤18 years old) with cytologically benign thyroid nodules evaluated between 1998 and 2016.
Cytologically benign nodules (N = 237) in 181 patients were followed by ultrasound (median follow-up, 3.4 years; range, 0.5 to 13.9 years) or to resection. Thyroid cancer was diagnosed in six nodules (2.5%), and all six patients were disease free after median follow-up of 4.9 years. Malignancy was more common in nodules >4 cm (15.4%; P = 0.037) or that grew during follow-up (6.0%; P = 0.048). The likelihood of nodule growth (±SE) was 15% ± 3%, 24% ± 4%, and 49% ± 10% at 6, 12, and 24 months, respectively. Among nodules >2 cm, those with ≥25% cystic content grew more slowly than nodules <25% cystic; nodules <2 cm grew similarly regardless of cystic content.
Benign cytology in pediatric thyroid nodules has a low false-negative rate similar to that in adults, and prognosis is excellent in the rare cases of malignancy. Resection of nodules >4 cm, combined with surveillance of smaller nodules and repeated aspiration for growth, detects most false-negative results. Follow-up ultrasound in 12 months is appropriate for most cytologically benign pediatric nodules, but delaying surveillance up to 24 months may be reasonable in large, predominantly cystic nodules.
大多数儿科甲状腺结节的细胞学表现为良性,但目前仅有少量数据可用于指导治疗。
描述细胞学良性的儿科甲状腺结节的自然病程和结局。
队列研究。
学术医疗中心的多学科甲状腺诊所。
1998 年至 2016 年连续就诊的细胞学良性甲状腺结节的儿科患者(≤18 岁)。
181 例患者的 237 个细胞学良性结节接受了超声检查(中位随访时间为 3.4 年;范围 0.5~13.9 年)或接受了手术切除。在中位随访 4.9 年后,有 6 个结节(2.5%)被诊断为甲状腺癌,所有患者均无疾病复发。结节>4 cm(15.4%;P=0.037)或随访期间生长(6.0%;P=0.048)时更常见发生恶变。结节生长的可能性(±SE)分别为:6、12 和 24 个月时为 15%±3%、24%±4%和 49%±10%。结节>2 cm 时,囊性成分≥25%的结节生长速度较慢,而囊性成分<25%的结节则无差异;结节<2 cm 时,无论囊性成分如何,生长速度相似。
儿科甲状腺结节的良性细胞学检查有与成人相似的低假阴性率,且在罕见的恶性肿瘤病例中预后极好。对于>4 cm 的结节,切除结合对较小结节的监测和对生长结节的重复抽吸,可以发现大多数假阴性结果。对于大多数细胞学良性的儿科结节,12 个月的随访超声是合适的,但对于大的、以囊性为主的结节,延迟至 24 个月的监测可能是合理的。