Case Report
Progressive left cervical mass in an infant diagnosed as neuroglial heterotopia: A case report
Submitted: 23 May 2026 | Published: 31 July 2026
About the author(s)
Alaipreet Kaur, Department of Radiodiagnosis, Division of Neuroimaging and Interventional Neuroradiology, Post Graduate Institute of Medical Education and Research, IndiaSameer Vyas, Department of Radiodiagnosis, Division of Neuroimaging and Interventional Neuroradiology, Post Graduate Institute of Medical Education and Research, Chandigarh, India
Atul Jain, Department of Histopathology, Post Graduate Institute of Medical Education and Research, Chandigarh, India
Hemlata Jangir, Department of Histopathology, Post Graduate Institute of Medical Education and Research, Chandigarh, India
Abstract
Neuroglial heterotopia is a congenital developmental anomaly characterised by mature glial tissue located outside the cranial cavity or spinal canal, without intracranial communication. A 12-month-old girl presented with an enlarging left cervical mass and worsening respiratory symptoms. MRI demonstrated a trans-spatial, multiseptated cystic lesion in the left parotid and submandibular spaces, extending medially into the parapharyngeal space with upper airway compression. No intracranial communication was identified. The postoperative specimen revealed mature glial tissue interspersed within fibroconnective stroma, confirming neuroglial heterotopia.
Contribution: This case highlights the importance of considering neuroglial heterotopia in the differential diagnosis for congenital or progressive cystic neck masses in infants. Although MRI plays a central role in defining the lesion extent, a definitive diagnosis requires histopathological confirmation.
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