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DOI 10.1080/13816810.2020.1810281

Медицинская библиотека · Ophthalmic genetics · 2020

Genomic analysis of adult case of ocular surface giant congenital melanocytic nevus and associated clinicopathological findings.

McGrath Lindsay A, Palmer Jane M, Stark Andrew, Glasson William, Warrier Sunil K, Whitehead Kevin, Hamilton Hayley, Brooks Kelly, Johansson Peter A, Hayward Nicholas K

Клинический случайСтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

INTRODUCTION

Conjunctival nevi are the most common tumor of the ocular surface. There are some rare reports of so-called 'giant' conjunctival nevi. We report a case of a 47-year-old female with a cutaneous and ocular surface giant congenital melanocytic nevus and describe her clinical course.

CASE DESCRIPTION: This is a retrospective case report of a single patient. A 47-year-old female with a history of biopsy-proven periorbital congenital melanocytic nevus, with an associated giant conjunctival nevus presented for structural and functional rehabilitation. Serial surgeries were performed and excised tissue was sent for histopathological and genetic examination. The conjunctival nevus had a low tumor mutation burden, and of the 647 somatic mutations, only one occurred within a protein coding region, namely NRAS p.Gln61Arg.

CONCLUSION

This is the first reported adult case including genomic analysis of an ocular surface giant congenital melanocytic nevus. The case shows a possible association between periorbital congenital melanocytic nevi and giant conjunctival nevi, and underscores the possible role that targeted drug therapies may have in malignant transformation of these conditions.

Для цитирования: McGrath Lindsay A, Palmer Jane M, Stark Andrew, Glasson William, Warrier Sunil K, Whitehead Kevin, Hamilton Hayley, Brooks Kelly, Johansson Peter A, Hayward Nicholas K. Genomic analysis of adult case of ocular surface giant congenital melanocytic nevus and associated clinicopathological findings.. Ophthalmic genetics. 2020. DOI: 10.1080/13816810.2020.1810281.

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