Patel Siddharth, Kunnath Ansley J, Gallant Jean-Nicolas, Belcher Ryan H
Vanderbilt University Medical Scholars Program Nashville Tennessee USA.
Meharry Medical College Nashville Tennessee USA.
OTO Open. 2023 Aug 9;7(3):e66. doi: 10.1002/oto2.66. eCollection 2023 Jul-Sep.
To perform a scoping review to characterize postoperative outcomes of pediatric patients (ages 0-18) with a history of congenital head and neck teratomas.
PubMed, EMBASE, Web of Science, Cochrane, Clinicaltrails.gov.
A search of multiple databases was performed. Studies were included if they detailed the surgical management and outcomes of pediatric patients with a history of congenital head and neck teratomas.
One hundred and eight studies totaling 137 patients were identified. The median gestational age at birth was 37 weeks. Respiratory distress, prompting emergent endotracheal intubation or tracheostomy, was present in most patients (58%). The ex utero intrapartum treatment (EXIT) procedure was utilized for 21 (15%) patients. The teratomas were resected after a median duration of 4 days from birth. The most common postsurgical complications were vocal cord paralysis (3%), hemorrhage (2%), and tracheomalacia (2%). Death occurred perioperatively in 2 patients (2%). Twenty-six patients (19%) required additional surgery, and 5 patients (4%) needed adjuvant chemotherapy. Patients were monitored for a median duration of 24 months with a recurrence rate of 6%. Four recurrent cases (50%) had intracranial extension, and 88% of the recurrent cases were mature teratomas at initial histopathological diagnosis.
Most patients with congenital head and neck teratomas require emergent airway management perinatally. Excisional and surgical complications are rare, and most patients are cured of their disease with a single operation. Recurrent teratomas tend to have an intracranial extension and are likely to be of mature pathology at the time of initial diagnosis.
进行一项范围综述,以描述有先天性头颈部畸胎瘤病史的儿科患者(0至18岁)的术后结局。
PubMed、EMBASE、科学网、Cochrane、Clinicaltrails.gov。
对多个数据库进行检索。纳入的研究需详细描述有先天性头颈部畸胎瘤病史的儿科患者的手术管理及结局。
共识别出108项研究,涉及137例患者。出生时的中位孕周为37周。大多数患者(58%)出现呼吸窘迫,需要紧急气管插管或气管切开。21例(15%)患者采用了产时宫外治疗(EXIT)手术。畸胎瘤在出生后中位4天进行切除。最常见的术后并发症为声带麻痹(3%)、出血(2%)和气管软化(2%)。围手术期有2例患者(2%)死亡。26例患者(19%)需要再次手术,5例患者(4%)需要辅助化疗。患者中位随访24个月,复发率为6%。4例复发病例(50%)有颅内扩展,88%的复发病例在初始组织病理学诊断时为成熟畸胎瘤。
大多数有先天性头颈部畸胎瘤的患者在围产期需要紧急气道管理。切除及手术并发症罕见,大多数患者通过单次手术治愈疾病。复发性畸胎瘤往往有颅内扩展,且在初始诊断时可能为成熟病理类型。