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Primary Transpupillary Thermotherapy of Choroidal Melanocytic Lesions

PURPOSE: To evaluate the role of primary transpupillary thermotherapy (TTT) in the treatment of choroidal melanocytic lesions. MATERIALS AND METHODS: Retrospective chart review of 24 patients (24 eyes) with choroidal melanocytic lesions, including 20 choroidal melanoma and four choroidal nevus treat...

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Autores principales: Gündüz, Kaan, Karslioğlu, Melisa Zişan, Köse, Kenan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3119291/
https://www.ncbi.nlm.nih.gov/pubmed/21731333
http://dx.doi.org/10.4103/0974-9233.80711
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author Gündüz, Kaan
Karslioğlu, Melisa Zişan
Köse, Kenan
author_facet Gündüz, Kaan
Karslioğlu, Melisa Zişan
Köse, Kenan
author_sort Gündüz, Kaan
collection PubMed
description PURPOSE: To evaluate the role of primary transpupillary thermotherapy (TTT) in the treatment of choroidal melanocytic lesions. MATERIALS AND METHODS: Retrospective chart review of 24 patients (24 eyes) with choroidal melanocytic lesions, including 20 choroidal melanoma and four choroidal nevus treated with primary TTT. Choroidal nevus cases treated with primary TTT either demonstrated risk factors for growth into an early melanoma or had overlying choroidal neovascularization. RESULTS: The mean initial tumor basal diameter was 6.6 (3.0-10.0) mm and the mean initial tumor thickness was 3.0 (1.0-5.0) mm. The mean number of TTT sessions was 2.5 (1-6). The mean decrease in tumor thickness was 1.2 mm (from 3.0 to 1.8 mm) at a mean follow-up of 22.7 (range 3-90) months. On the LogMar scale, visual acuity was stable at 1.0. Complications occurred in 50% of eyes. The most frequent complications were vitreous hemorrhage [5 patients (20.8%)], focal cataract [5 patients (20.8%)], iris atrophy [4 patients (16.6%)] and posterior synechia [4 patients (16.6%)]. There was no significant difference in the complication rate with respect to tumor thickness >3 mm versus tumor thickness ≤3 mm and juxtapapillary versus nonjuxtapapillary location (Fisher’s exact test, P>0.05). Kaplan-Meier curves showed that 9% of eyes develop recurrence by 1 year and 27% develop recurrence by 5 years after primary TTT. Two eyes (8.3%) were enucleated because of neovascular glaucoma and one eye (4.1%) was exenterated because of extraocular tumor recurrence. Globe salvage was achieved in 21 patients (87.5%). One patient (4.1%) with extraocular tumor recurrence developed liver metastasis and expired. CONCLUSIONS: Although TTT may be useful in the treatment of small choroidal melanocytic lesions, the high complication and recurrence rates warrant close monitoring of patients after primary TTT even when a flat chorioretinal scar has been achieved.
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spelling pubmed-31192912011-06-30 Primary Transpupillary Thermotherapy of Choroidal Melanocytic Lesions Gündüz, Kaan Karslioğlu, Melisa Zişan Köse, Kenan Middle East Afr J Ophthalmol Original Article PURPOSE: To evaluate the role of primary transpupillary thermotherapy (TTT) in the treatment of choroidal melanocytic lesions. MATERIALS AND METHODS: Retrospective chart review of 24 patients (24 eyes) with choroidal melanocytic lesions, including 20 choroidal melanoma and four choroidal nevus treated with primary TTT. Choroidal nevus cases treated with primary TTT either demonstrated risk factors for growth into an early melanoma or had overlying choroidal neovascularization. RESULTS: The mean initial tumor basal diameter was 6.6 (3.0-10.0) mm and the mean initial tumor thickness was 3.0 (1.0-5.0) mm. The mean number of TTT sessions was 2.5 (1-6). The mean decrease in tumor thickness was 1.2 mm (from 3.0 to 1.8 mm) at a mean follow-up of 22.7 (range 3-90) months. On the LogMar scale, visual acuity was stable at 1.0. Complications occurred in 50% of eyes. The most frequent complications were vitreous hemorrhage [5 patients (20.8%)], focal cataract [5 patients (20.8%)], iris atrophy [4 patients (16.6%)] and posterior synechia [4 patients (16.6%)]. There was no significant difference in the complication rate with respect to tumor thickness >3 mm versus tumor thickness ≤3 mm and juxtapapillary versus nonjuxtapapillary location (Fisher’s exact test, P>0.05). Kaplan-Meier curves showed that 9% of eyes develop recurrence by 1 year and 27% develop recurrence by 5 years after primary TTT. Two eyes (8.3%) were enucleated because of neovascular glaucoma and one eye (4.1%) was exenterated because of extraocular tumor recurrence. Globe salvage was achieved in 21 patients (87.5%). One patient (4.1%) with extraocular tumor recurrence developed liver metastasis and expired. CONCLUSIONS: Although TTT may be useful in the treatment of small choroidal melanocytic lesions, the high complication and recurrence rates warrant close monitoring of patients after primary TTT even when a flat chorioretinal scar has been achieved. Medknow Publications 2011 /pmc/articles/PMC3119291/ /pubmed/21731333 http://dx.doi.org/10.4103/0974-9233.80711 Text en © Middle East African Journal of Ophthalmology http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Gündüz, Kaan
Karslioğlu, Melisa Zişan
Köse, Kenan
Primary Transpupillary Thermotherapy of Choroidal Melanocytic Lesions
title Primary Transpupillary Thermotherapy of Choroidal Melanocytic Lesions
title_full Primary Transpupillary Thermotherapy of Choroidal Melanocytic Lesions
title_fullStr Primary Transpupillary Thermotherapy of Choroidal Melanocytic Lesions
title_full_unstemmed Primary Transpupillary Thermotherapy of Choroidal Melanocytic Lesions
title_short Primary Transpupillary Thermotherapy of Choroidal Melanocytic Lesions
title_sort primary transpupillary thermotherapy of choroidal melanocytic lesions
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3119291/
https://www.ncbi.nlm.nih.gov/pubmed/21731333
http://dx.doi.org/10.4103/0974-9233.80711
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