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Removal of a congenital corneal dermoid through tumor excision and lamellar keratoplasty in a young child: A case report

RATIONALE: Corneal dermoids are a rare cause of corneal opacification, consisting of abnormal mesoblastic tissue surrounded by epithelium. Here, we describe the case of a 1-year-old child who had a congenital corneal dermoid in the left eye since birth; thus, the patient underwent tumor excision fol...

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Autores principales: Cui, Yanyan, Yin, Shan, Yin, Xuewei, Liu, Yonghui, Zhao, Bojun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8663910/
https://www.ncbi.nlm.nih.gov/pubmed/34889242
http://dx.doi.org/10.1097/MD.0000000000027981
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author Cui, Yanyan
Yin, Shan
Yin, Xuewei
Liu, Yonghui
Zhao, Bojun
author_facet Cui, Yanyan
Yin, Shan
Yin, Xuewei
Liu, Yonghui
Zhao, Bojun
author_sort Cui, Yanyan
collection PubMed
description RATIONALE: Corneal dermoids are a rare cause of corneal opacification, consisting of abnormal mesoblastic tissue surrounded by epithelium. Here, we describe the case of a 1-year-old child who had a congenital corneal dermoid in the left eye since birth; thus, the patient underwent tumor excision followed by keratoplasty. PATIENT CONCERN: A 1-year-old girl was brought to the hospital by her parents, who had been noticing a mass on the surface of her left eyeball since birth. The patient had no other previous or concurrent disease nor family history for dermoids. CLINICAL FINDINGS: No abnormalities were present in the cornea and the anterior and posterior segments of the right eye. Eye movement, intraocular pressure, and the position of the upper eyelid of the left eye were normal. No signs of conjunctival hyperemia were present. The tumor presented as a yellowish-pink mass with hair and veins on the surface. DIAGNOSE: The patient was initially diagnosed with a keratoconjunctival tumor of the left eye by a clinical doctor. INTERVENTIONS: Corneal tumor resection combined with keratoplasty was performed in the patient. Eye drops with 1% cyclosporine were administered 3 times per day to prevent immune rejection. OUTCOMES: Based on postoperative pathological examinations, the final diagnosis was a corneal dermoid. The patient had an uneventful healing process and rapid corneal re-epithelization. The ocular surface was stable during the follow-up visits, and no complications emerged. LESSONS: We report a rare case of congenital corneal dermoid. We learned that close follow-up is needed after surgery in such cases.
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spelling pubmed-86639102021-12-13 Removal of a congenital corneal dermoid through tumor excision and lamellar keratoplasty in a young child: A case report Cui, Yanyan Yin, Shan Yin, Xuewei Liu, Yonghui Zhao, Bojun Medicine (Baltimore) 5800 RATIONALE: Corneal dermoids are a rare cause of corneal opacification, consisting of abnormal mesoblastic tissue surrounded by epithelium. Here, we describe the case of a 1-year-old child who had a congenital corneal dermoid in the left eye since birth; thus, the patient underwent tumor excision followed by keratoplasty. PATIENT CONCERN: A 1-year-old girl was brought to the hospital by her parents, who had been noticing a mass on the surface of her left eyeball since birth. The patient had no other previous or concurrent disease nor family history for dermoids. CLINICAL FINDINGS: No abnormalities were present in the cornea and the anterior and posterior segments of the right eye. Eye movement, intraocular pressure, and the position of the upper eyelid of the left eye were normal. No signs of conjunctival hyperemia were present. The tumor presented as a yellowish-pink mass with hair and veins on the surface. DIAGNOSE: The patient was initially diagnosed with a keratoconjunctival tumor of the left eye by a clinical doctor. INTERVENTIONS: Corneal tumor resection combined with keratoplasty was performed in the patient. Eye drops with 1% cyclosporine were administered 3 times per day to prevent immune rejection. OUTCOMES: Based on postoperative pathological examinations, the final diagnosis was a corneal dermoid. The patient had an uneventful healing process and rapid corneal re-epithelization. The ocular surface was stable during the follow-up visits, and no complications emerged. LESSONS: We report a rare case of congenital corneal dermoid. We learned that close follow-up is needed after surgery in such cases. Lippincott Williams & Wilkins 2021-12-10 /pmc/articles/PMC8663910/ /pubmed/34889242 http://dx.doi.org/10.1097/MD.0000000000027981 Text en Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/)
spellingShingle 5800
Cui, Yanyan
Yin, Shan
Yin, Xuewei
Liu, Yonghui
Zhao, Bojun
Removal of a congenital corneal dermoid through tumor excision and lamellar keratoplasty in a young child: A case report
title Removal of a congenital corneal dermoid through tumor excision and lamellar keratoplasty in a young child: A case report
title_full Removal of a congenital corneal dermoid through tumor excision and lamellar keratoplasty in a young child: A case report
title_fullStr Removal of a congenital corneal dermoid through tumor excision and lamellar keratoplasty in a young child: A case report
title_full_unstemmed Removal of a congenital corneal dermoid through tumor excision and lamellar keratoplasty in a young child: A case report
title_short Removal of a congenital corneal dermoid through tumor excision and lamellar keratoplasty in a young child: A case report
title_sort removal of a congenital corneal dermoid through tumor excision and lamellar keratoplasty in a young child: a case report
topic 5800
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8663910/
https://www.ncbi.nlm.nih.gov/pubmed/34889242
http://dx.doi.org/10.1097/MD.0000000000027981
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