Kharsi Noha Kiki, Naser Majd, Hammad Alaa, Shaheen Zein, Alassaf Areej
Faculty of Medicine of Damascus University, Damascus, Syria.
Faculty of Medicine of Damascus University, Damascus, Syria.
Int J Surg Case Rep. 2024 Oct;123:110227. doi: 10.1016/j.ijscr.2024.110227. Epub 2024 Sep 3.
Neuroglial heterotopia represents a rare differential diagnosis for pediatric neck masses. Its occurrence in the parapharyngeal space is exceptionally uncommon, with fewer than 30 documented cases in the literature.
This report details the case of a 4-year-old girl initially noted to have a mass in the right parotid area at birth with no symptoms. After observation, she returned at the age of 4 with dysphagia and a visible mass in the same area. Subsequent CT imaging revealed a mass in the right parapharyngeal space, prompting surgical intervention. Histological examination after resection confirmed the diagnosis of neuroglial heterotopia.
Neuroglial heterotopia manifests with various symptoms in pediatric patients, posing diagnostic challenges due to the lack of specific radiological or clinical features distinguishing it from other neck masses in children.
This case highlights the significance of considering neuroglial heterotopia in pediatric neck region masses diagnoses. Further research is needed to better understand its clinical features and treatment options.
神经胶质异位是小儿颈部肿块一种罕见的鉴别诊断。其发生于咽旁间隙极为罕见,文献记载病例不足30例。
本报告详细介绍了一名4岁女孩的病例,该女孩出生时最初被发现右侧腮腺区有一肿块,无症状。观察后,她4岁时因吞咽困难和同一区域出现可见肿块前来就诊。随后的CT成像显示右侧咽旁间隙有一肿块,促使进行手术干预。切除后的组织学检查确诊为神经胶质异位。
神经胶质异位在儿科患者中表现出各种症状,由于缺乏将其与儿童其他颈部肿块区分开来的特异性影像学或临床特征,给诊断带来了挑战。
本病例突出了在小儿颈部区域肿块诊断中考虑神经胶质异位的重要性。需要进一步研究以更好地了解其临床特征和治疗选择。