Journal of Cutaneous and Aesthetic Surgery
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CASE REPORT
Year : 2020  |  Volume : 13  |  Issue : 3  |  Page : 233-236

A rare case of nasal glial heterotopia in an infant


Department of Pathology, University College of Medical Sciences, Delhi, India

Correspondence Address:
Nadeem Tanveer
Department of Pathology, University College of Medical Sciences, Delhi.
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/JCAS.JCAS_148_19

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Glial heterotopias are the displacement of neuroglial tissue in extracranial sites. Nasal glial heterotopias can be of three types-extranasal, intranasal and mixed. Root of the nose is the most common location. These are rare anomalies with an incidence of 1 case in 20,000–40,000 live births. Here we report the case of a 6-month-old infant with a congenital mass located at the root of the nose. Non-contrast computed tomography studies showed no evidence of intracranial communication of the lesion. The mass was excised, and on histopathological examination, it showed glial tissue with astrocytes in a fibrillary background and fibroconnective tissue. Masson’s trichrome stain showed the red staining of the glial tissue, whereas the background fibrosis was stained blue. On immunohistochemistry, glial fibrillary acidic protein was positive. Hence, the diagnosis of nasal glial heterotropia was made. The patient had an uneventful postoperative period.


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