Early recurrent neonatal tongue glial heterotopia presenting with acute airway obstruction: the first case report
Junwei Zhao, Xiangrong Wang, Fan Yin, Jing Chu

TL;DR
This paper reports the first case of early recurrence of a rare tongue condition in a newborn, emphasizing the need for extensive surgery to prevent future issues.
Contribution
The first documented case of early recurrence of neonatal tongue glial heterotopia following conservative excision.
Findings
Incomplete conservative excision of tongue glial heterotopia can lead to rapid recurrence.
Extensive surgical resection with a 5-mm safety margin is necessary to prevent recurrence.
Early surgical intervention can stabilize neonates with airway obstruction and ensure long-term follow-up without complications.
Abstract
Glial heterotopia is a rare congenital developmental anomaly characterized by the presence of mature glial tissue outside the central nervous system. It most commonly affects the nasal region, while tongue involvement, particularly at the base of the tongue, is extremely uncommon. This case represented the first reported instance of early postoperative recurrence of tongue glial heterotopia. We described a 24-day-old male infant diagnosed with tongue glial heterotopia complicated by pneumonia and presenting with airway obstruction. The patient initially underwent conservative local excision of the lesion; however, the lesion rapidly recurred within three weeks postoperatively. A second, more extensive surgical resection with a 5-mm safety margin was subsequently performed. Histopathological examination of both specimens confirmed the diagnosis of glial heterotopia. This report…
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Taxonomy
TopicsTeratomas and Epidermoid Cysts · Spinal Dysraphism and Malformations · Fetal and Pediatric Neurological Disorders
