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Pathology of the Orbit: Neoplasms

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Albert and Jakobiec's Principles and Practice of Ophthalmology

Abstract

Orbital tumors constitute a heterogeneous group of neoplasms. A systemic approach allows for better understanding of their classification and clinical implications. Based on their origin, tumors occurring in the orbit are classified as primary neoplasms, which originate in the orbital structures/tissues themselves; secondary neoplasms, which extend by contiguity to the orbit from adjacent structures such as intracranial tumors and tumors of the paranasal sinuses; and metastatic neoplasms.

The primary orbital neoplasms are divided histologically into tumors of the lacrimal gland, tumors with mesenchymal differentiation, neoplasms arising in the orbital bones, lymphoproliferative and hematopoietic neoplasms, tumors originating in the optic nerve sheath, and tumors of uncertain etiology. In this chapter, classifications were based on the most current World Health Organization classification of tumors. For each neoplasm, we provide diagnostic criteria, based on gross and microscopic features, recommendations for usage of immunohistochemistry, and ancillary molecular testing to assist with the diagnosis and differentiation with other similar neoplasms. A summary of the clinical presentation, prevalence, and clinical behavior is also provided.

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Logunova, V., Roden, A.C., Salomão, D.R. (2021). Pathology of the Orbit: Neoplasms. In: Albert, D., Miller, J., Azar, D., Young, L.H. (eds) Albert and Jakobiec's Principles and Practice of Ophthalmology. Springer, Cham. https://doi.org/10.1007/978-3-319-90495-5_135-1

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