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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...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2019
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
Descripción
Sumario: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.