Primary orbital melanoma: a case series and literature review
- PMID: 29388848
- DOI: 10.1080/01676830.2017.1423354
Primary orbital melanoma: a case series and literature review
Erratum in
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Correction to: Figueira et al., Primary orbital melanoma: a case series and literature review.Orbit. 2018 Oct;37(5):i. doi: 10.1080/01676830.2018.1446728. Epub 2018 Mar 7. Orbit. 2018. PMID: 29513628 No abstract available.
Abstract
Primary orbital melanoma (POM) is a very rare condition. We report further four cases and review all previously reported cases. We present a multicentre retrospective review of patients with POM. Clinical, radiological, surgical, histological, and follow-up data is presented. Four patients with POM were identified between 2000 and 2013. All presented with proptosis and diplopia without reduced vision. Two had known pre-existing blue cell naevi. All were stage T1N0M0. All underwent exenteration with adjuvant radiotherapy. All are disease free at follow-up durations of 24-151 months. The present three cases and review of all cases in the literature suggest a higher likelihood of disease-free survival from primary exenteration (7/8 disease-free survival, 1/8 death from metastatic disease) than wide local excision (7/16 disease-free survival, 9 recurrence or metastasis of whom 4 died). Adjuvant radiotherapy may additionally improve outcomes.
Keywords: Adjuvant treatment; blue cellular naevus; congenital ocular melanocytosis; exenteration; orbit; primary orbital melanoma.
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