Stromal tumors

dc.contributor.author	Vemuganti, Geeta K.
dc.contributor.author	Honavar, Santosh G.
dc.date.accessioned	2022-03-27T04:11:38Z
dc.date.available	2022-03-27T04:11:38Z
dc.date.issued	2014-01-01
dc.description.abstract	Eyelid stromal tumors could be considered under several distinct categories based on the tissue of origin: fibrous tissue tumors, fibrohistiocytic tumors, lipomatous tumors, smooth muscle tumors, skeletal muscle tumors, vascular tumors, perivascular tumors, neural tumors, lymphoid, plasmacytic, and leukemic tumors, cartilage and bone tumors, secondary tumors, metastatic tumors, and hamartomas, choristomas, and other miscellaneous lesions. Some of the inflammatory and infective conditions such as chalazion, pyogenic granuloma, verruca vulgaris, and molluscum contagiosum may manifest with features clinically simulating tumors. This chapter describes the salient features and management of common eyelid stromal tumors.
dc.identifier.citation	Clinical Ophthalmic Oncology: Eyelid and Conjunctival Tumors
dc.identifier.uri	10.1007/978-3-642-38336-6_9
dc.identifier.uri	http://link.springer.com/10.1007/978-3-642-38336-6_9
dc.identifier.uri	https://dspace.uohyd.ac.in/handle/1/6786
dc.title	Stromal tumors
dc.type	Book. Book Chapter
dspace.entity.type

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