Corneoscleral locally aggressive fibrous histiocytoma in Xeroderma Pigmentosum patient: A case report

Xeroderma pigmentosum (XP) is a rare autosomal recessive disorder that has been found in all continents and racial groups in relation to faulty repair of DNA with sun exposure. Several cutaneous and ocular tumors have been described in relation to XP including fibrous histiocytoma (FH). The diagnosi...

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Detalles Bibliográficos
Autores principales: Alkatan, Hind M., Maktabi, Azza M.Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6819724/
https://www.ncbi.nlm.nih.gov/pubmed/31686974
http://dx.doi.org/10.1016/j.sjopt.2017.08.001

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6819724/
https://www.ncbi.nlm.nih.gov/pubmed/31686974
http://dx.doi.org/10.1016/j.sjopt.2017.08.001

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