Congenital Immature Orbital Teratoma with Sarcomatous Transformation Presenting as Exophthalmos: A case report

Background Congenital immature orbital teratomas are rare neoplasms, with intraorbital cases presenting unique diagnostic and therapeutic challenges. Case presentation This report presents a patient that exhibited rapid-growing right exophthalmos since birth. Imaging studies revealed a progressively expanding lesion in the right orbital cavity and optic nerve. Following partial resection and subsequent orbital exenteration, histopathological and immunohistochemical analyses confirmed the diagnosis of immature teratoma with sarcomatous transformation. The patient underwent chemotherapy and remains under surveillance with no signs of disease recurrence. Conclusion This case highlights the complexities associated with diagnosis and treatment of rare orbital teratomas, contributing valuably to the existing literature.

Authors

Publication Details

Journal
Journal of Neonatal Surgery
Published
2025-02-07
DOI
https://doi.org/10.52783/jns.v14.1605
Primary Topic
Teratomas and Epidermoid Cysts
Type
article
Field-Weighted Citation Impact
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article

Congenital Immature Orbital Teratoma with Sarcomatous Transformation Presenting as Exophthalmos: A case report

Júlia Costa Linhares, Samya Hamad Mehanna, Gregório Andreassa Soares
Journal of Neonatal Surgery
Teratomas and Epidermoid Cysts
article

Congenital Immature Orbital Teratoma with Sarcomatous Transformation Presenting as Exophthalmos: A case report

Júlia Costa Linhares, Samya Hamad Mehanna, Gregório Andreassa Soares
article en

Abstract

Background Congenital immature orbital teratomas are rare neoplasms, with intraorbital cases presenting unique diagnostic and therapeutic challenges. Case presentation This report presents a patient that exhibited rapid-growing right exophthalmos since birth. Imaging studies revealed a progressively expanding lesion in the right orbital cavity and optic nerve. Following partial resection and subsequent orbital exenteration, histopathological and immunohistochemical analyses confirmed the diagnosis of immature teratoma with sarcomatous transformation. The patient underwent chemotherapy and remains under surveillance with no signs of disease recurrence. Conclusion This case highlights the complexities associated with diagnosis and treatment of rare orbital teratomas, contributing valuably to the existing literature.

Journal of Neonatal SurgeryVol. 14(1S)
Openalex Percentile: Top 94%
Teratomas and Epidermoid Cysts
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