Iris melanoma relapsing sixteen years after proton-beam therapy: The importance of lifelong follow-up.

Ciliary body Irido-corneal angle Iris Melanoma Proton-beam therapy Radiotherapy

Journal

American journal of ophthalmology case reports
ISSN: 2451-9936
Titre abrégé: Am J Ophthalmol Case Rep
Pays: United States
ID NLM: 101679941

Informations de publication

Date de publication:
Mar 2019
Historique:
received: 28 08 2018
revised: 29 11 2018
accepted: 04 12 2018
entrez: 9 1 2019
pubmed: 9 1 2019
medline: 9 1 2019
Statut: epublish

Résumé

To report a case of locally recurrent spindle-cell iris amelanotic melanoma 16 years after proton-beam therapy. In 2001, a 45-year-old man presented with an amelanotic iris melanoma, extending from the 5 to 10 o'clock positions on his left eye. High-frequency ultrasonography showed extension of melanoma into the ciliary body. He was initially managed with proton-beam therapy (60 Gy delivered in four fractions over four consecutive days) and underwent ocular and systemic examination at regular intervals over the following years. Local tumor control was achieved, and the patient did not develop metastasis during sixteen consecutive years. In 2017, 16 years after he received proton-beam therapy, the patient developed a focal amelanotic lesion strongly suggestive of a local recurrence of iris melanoma, although it extended from the 1 to 6 o'clock positions. He also presented with treatment-resistant glaucoma with an intraocular pressure (IOP) of 37 mmHg, despite maximal topical IOP-lowering therapy. Since a second irradiation of the anterior segment was contraindicated, the eye was enucleated. Pathological analysis confirmed the diagnosis of iris melanoma and demonstrated iridocorneal angle invasion extending from the initial site to the recurrent tumor location. Regular ophthalmological surveillance for life with gonioscopy and high-frequency ultrasonography is recommended in patients with iris melanoma, due to the possibility of delayed local recurrence more than a decade after the initial treatment.

Identifiants

pubmed: 30619969
doi: 10.1016/j.ajoc.2018.12.007
pii: S2451-9936(18)30377-3
pmc: PMC6305799
doi:

Types de publication

Case Reports

Langues

eng

Pagination

89-92

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Auteurs

Laetitia-Claire Msika (LC)

Institut Curie, PSL Research University, Department of Ophthalmology, F-75005, Paris, France.

Laurence Desjardins (L)

Institut Curie, PSL Research University, Department of Ophthalmology, F-75005, Paris, France.

Vincent Cockenpot (V)

Institut Curie, PSL Research University, Department of Pathology, F-75005, Paris, France.

Rémi Dendale (R)

Institut Curie, PSL Research University, Department of Radiation Therapy, F-75005, Paris, France.

Olivier Berges (O)

Fondation Ophtalmologique Adolphe de Rothschild, Department of Medical Imaging, F-75019, Paris, France.

Khadija Aït Raïs (K)

Institut Curie, PSL Research University, Somatic Genetic Unit, Department of Genetic, F-75005, Paris, France.

Gaëlle Pierron (G)

Institut Curie, PSL Research University, Somatic Genetic Unit, Department of Genetic, F-75005, Paris, France.

Raymond L Barnhill (RL)

Institut Curie, PSL Research University, Department of Pathology, F-75005, Paris, France.

Nathalie Cassoux (N)

Institut Curie, PSL Research University, Department of Ophthalmology, F-75005, Paris, France.
Université Paris Descartes, Sorbonne Paris Cité, F-75005, Paris, France.

Alexandre Matet (A)

Institut Curie, PSL Research University, Department of Ophthalmology, F-75005, Paris, France.
Université Paris Descartes, Sorbonne Paris Cité, F-75005, Paris, France.

Classifications MeSH