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Giant Ocular Lipodermoid Cyst in Encephalocraniocutaneous Lipomatosis: Surgical Treatment and Genetic Analysis
Patient: Female, 11 Final Diagnosis: Encephalocraniocutaneous lipomatosis Symptoms: Conjunctivitis • Ocular irritation Medication: — Clinical Procedure: Excisional biopsy Specialty: Ophthalmology OBJECTIVE: Rare disease BACKGROUND: Encephalocraniocutaneous lipomatosis is a rare neurocutaneous disord...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6824416/ https://www.ncbi.nlm.nih.gov/pubmed/31649234 http://dx.doi.org/10.12659/AJCR.918684 |
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author | Córdoba, Andrea Graue-Hernández, Enrique O. Navas, Alejandro Chacon-Camacho, Oscar F. Zenteno, Juan C. Ramirez-Miranda, Arturo Bermudez-Magner, Jose Antonio Ordaz-Robles, Thania Pérez-Solórzano, Sofia Olivo-Payne, Andrew |
author_facet | Córdoba, Andrea Graue-Hernández, Enrique O. Navas, Alejandro Chacon-Camacho, Oscar F. Zenteno, Juan C. Ramirez-Miranda, Arturo Bermudez-Magner, Jose Antonio Ordaz-Robles, Thania Pérez-Solórzano, Sofia Olivo-Payne, Andrew |
author_sort | Córdoba, Andrea |
collection | PubMed |
description | Patient: Female, 11 Final Diagnosis: Encephalocraniocutaneous lipomatosis Symptoms: Conjunctivitis • Ocular irritation Medication: — Clinical Procedure: Excisional biopsy Specialty: Ophthalmology OBJECTIVE: Rare disease BACKGROUND: Encephalocraniocutaneous lipomatosis is a rare neurocutaneous disorder characterized by cutaneous, ocular, and central nervous system anomalies; its molecular etiology was recently identified. This report describes the surgical treatment and genetic characterization of a giant ocular lipodermoid cyst secondary to encephalocraniocutaneous lipomatosis. CASE REPORT: An 11-year-old girl with past medical history of absence seizures presented with a reddish protruding mass in her right eye involving the temporal conjunctiva and the peripheral temporal cornea; eyelid closure was not possible due to mass protrusion. She also presented skin tags at the level of the external canthus and 3 alopecic areas at the level of the scalp compatible with nevus psiloliparus. No family history was reported. A dermoid cyst was suspected and excisional biopsy was performed under general anesthesia. A large conjunctival and lamellar corneoscleral resection was done, followed by a corneal tectonic graft. Molecular analysis was carried out, including PCR and Sanger sequencing on DNA obtained from the mass. After surgery, the patient achieved complete eyelid closure, reduction of ocular surface symptoms, and improved aesthetic appearance. Histological analysis confirmed a lipodermoid cyst; genetic tests confirmed a mosaic activating mutation in FGFR1 (c.1638C>A, p.Asn546Lys). The diagnosis was encephalocraniocutaneous lipomatosis. CONCLUSIONS: ECCL is a rare condition; an accurate diagnosis comprising clinical and genetic aspects can facilitate the monitoring of possible complications, improve the multidisciplinary treatment, and provide valuable information for future therapy developments. In this case, the patient’s quality of life improved significantly, ocular symptoms disappeared, and a good esthetic appearance was achieved. |
format | Online Article Text |
id | pubmed-6824416 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | International Scientific Literature, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68244162019-11-14 Giant Ocular Lipodermoid Cyst in Encephalocraniocutaneous Lipomatosis: Surgical Treatment and Genetic Analysis Córdoba, Andrea Graue-Hernández, Enrique O. Navas, Alejandro Chacon-Camacho, Oscar F. Zenteno, Juan C. Ramirez-Miranda, Arturo Bermudez-Magner, Jose Antonio Ordaz-Robles, Thania Pérez-Solórzano, Sofia Olivo-Payne, Andrew Am J Case Rep Articles Patient: Female, 11 Final Diagnosis: Encephalocraniocutaneous lipomatosis Symptoms: Conjunctivitis • Ocular irritation Medication: — Clinical Procedure: Excisional biopsy Specialty: Ophthalmology OBJECTIVE: Rare disease BACKGROUND: Encephalocraniocutaneous lipomatosis is a rare neurocutaneous disorder characterized by cutaneous, ocular, and central nervous system anomalies; its molecular etiology was recently identified. This report describes the surgical treatment and genetic characterization of a giant ocular lipodermoid cyst secondary to encephalocraniocutaneous lipomatosis. CASE REPORT: An 11-year-old girl with past medical history of absence seizures presented with a reddish protruding mass in her right eye involving the temporal conjunctiva and the peripheral temporal cornea; eyelid closure was not possible due to mass protrusion. She also presented skin tags at the level of the external canthus and 3 alopecic areas at the level of the scalp compatible with nevus psiloliparus. No family history was reported. A dermoid cyst was suspected and excisional biopsy was performed under general anesthesia. A large conjunctival and lamellar corneoscleral resection was done, followed by a corneal tectonic graft. Molecular analysis was carried out, including PCR and Sanger sequencing on DNA obtained from the mass. After surgery, the patient achieved complete eyelid closure, reduction of ocular surface symptoms, and improved aesthetic appearance. Histological analysis confirmed a lipodermoid cyst; genetic tests confirmed a mosaic activating mutation in FGFR1 (c.1638C>A, p.Asn546Lys). The diagnosis was encephalocraniocutaneous lipomatosis. CONCLUSIONS: ECCL is a rare condition; an accurate diagnosis comprising clinical and genetic aspects can facilitate the monitoring of possible complications, improve the multidisciplinary treatment, and provide valuable information for future therapy developments. In this case, the patient’s quality of life improved significantly, ocular symptoms disappeared, and a good esthetic appearance was achieved. International Scientific Literature, Inc. 2019-10-25 /pmc/articles/PMC6824416/ /pubmed/31649234 http://dx.doi.org/10.12659/AJCR.918684 Text en © Am J Case Rep, 2019 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) ) |
spellingShingle | Articles Córdoba, Andrea Graue-Hernández, Enrique O. Navas, Alejandro Chacon-Camacho, Oscar F. Zenteno, Juan C. Ramirez-Miranda, Arturo Bermudez-Magner, Jose Antonio Ordaz-Robles, Thania Pérez-Solórzano, Sofia Olivo-Payne, Andrew Giant Ocular Lipodermoid Cyst in Encephalocraniocutaneous Lipomatosis: Surgical Treatment and Genetic Analysis |
title | Giant Ocular Lipodermoid Cyst in Encephalocraniocutaneous Lipomatosis: Surgical Treatment and Genetic Analysis |
title_full | Giant Ocular Lipodermoid Cyst in Encephalocraniocutaneous Lipomatosis: Surgical Treatment and Genetic Analysis |
title_fullStr | Giant Ocular Lipodermoid Cyst in Encephalocraniocutaneous Lipomatosis: Surgical Treatment and Genetic Analysis |
title_full_unstemmed | Giant Ocular Lipodermoid Cyst in Encephalocraniocutaneous Lipomatosis: Surgical Treatment and Genetic Analysis |
title_short | Giant Ocular Lipodermoid Cyst in Encephalocraniocutaneous Lipomatosis: Surgical Treatment and Genetic Analysis |
title_sort | giant ocular lipodermoid cyst in encephalocraniocutaneous lipomatosis: surgical treatment and genetic analysis |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6824416/ https://www.ncbi.nlm.nih.gov/pubmed/31649234 http://dx.doi.org/10.12659/AJCR.918684 |
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