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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...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Elsevier
2019
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| 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 |