Recurrent Solitary Neurofibroma Involving the Proximal Lacrimal Drainage System

Solitary eyelid neurofibroma is a rare condition, and there have been no reported cases of solitary eyelid neurofibroma involving the proximal lacrimal drainage system. A 6-year-old male presented with recurrent painless swelling in the medial part of the left lower eyelid. The patient was misdiagnosed as eyelid polyp and underwent excision biopsy twice elsewhere. Subsequently, the patient presented with a recurrence of swelling and was treated with full-thickness eyelid resection and reconstruction by direct closure. Histopathology showed the presence of spindle cells with hyperchromatic nuclei in a myxoid background. These cells showed S100 and CD 34 positivity. The systemic evaluation did not show any signs of neurofibromatosis.

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Publication Details

Journal
Ophthalmic Plastic and Reconstructive Surgery
Published
2024-11-19
DOI
https://doi.org/10.1097/iop.0000000000002820
Primary Topic
Neurofibromatosis and Schwannoma Cases
Type
article
Field-Weighted Citation Impact
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article

Recurrent Solitary Neurofibroma Involving the Proximal Lacrimal Drainage System

Mohammad Javed Ali, Saumya Jakati, Lavanya Maddi
Ophthalmic Plastic and Reconstructive Surgery
Neurofibromatosis and Schwannoma Cases
article

Recurrent Solitary Neurofibroma Involving the Proximal Lacrimal Drainage System

Mohammad Javed Ali, Saumya Jakati, Lavanya Maddi
article en

Abstract

Solitary eyelid neurofibroma is a rare condition, and there have been no reported cases of solitary eyelid neurofibroma involving the proximal lacrimal drainage system. A 6-year-old male presented with recurrent painless swelling in the medial part of the left lower eyelid. The patient was misdiagnosed as eyelid polyp and underwent excision biopsy twice elsewhere. Subsequently, the patient presented with a recurrence of swelling and was treated with full-thickness eyelid resection and reconstruction by direct closure. Histopathology showed the presence of spindle cells with hyperchromatic nuclei in a myxoid background. These cells showed S100 and CD 34 positivity. The systemic evaluation did not show any signs of neurofibromatosis.

Ophthalmic Plastic and Reconstructive SurgeryVol. 41(2)
L V Prasad Eye Institute (IN)
Openalex Percentile: Top 67%
Neurofibromatosis and Schwannoma Cases
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