Epibulbar osseous choristomaa clinicopathological case series and review of the literature

Détails

Ressource 1Télécharger: BIB_B9950925F74B.P001.pdf (13733.82 [Ko])
Etat: Public
Version: Après imprimatur
ID Serval
serval:BIB_B9950925F74B
Type
Mémoire
Sous-type
(Mémoire de) maîtrise (master)
Collection
Publications
Institution
Titre
Epibulbar osseous choristomaa clinicopathological case series and review of the literature
Auteur(s)
Vachette M.
Directeur(s)
Schalenbourg A.
Codirecteur(s)
Zografos L.
Détails de l'institution
Université de Lausanne, Faculté de biologie et médecine
Statut éditorial
Acceptée
Date de publication
2011
Langue
anglais
Nombre de pages
14
Résumé
Background:¦Choristomas are benign, congenital tumours composed of normal tissue in an¦abnormal location. Osseous choristomas represent the rarest form of epibulbar choristomas,¦with now 65 cases reported in the literature. We did a retrospective clinicopathological study¦of all patients with epibulbar osseous choristoma observed at our institution since 1982 and¦updated the last review of the literature.¦History and Signs:¦Three Caucasian male patients, aged between 3 months and 11 years,¦were identified. All osseous choristomas were located under the superotemporal bulbar¦conjunctiva of the right eye.¦Therapy and Outcome:¦All lesions were managed with surgical excision. Histopathology¦revealed the presence of lamellar bone in all cases, one of which was associated with a¦dermolipoma.¦Conclusions:¦We report a small rare case series of 3 epibulbar osseous choristomas and did a¦review of the literature. In one patient, the osteoma was associated with a dermolipoma,¦corresponding to the fourth reported complex choristoma of this type, in an otherwise normal¦eye, in the literature.
Mots-clé
Osteoma, choristoma, dermolipoma, epibulbar, bone and bones
Création de la notice
21/05/2012 12:52
Dernière modification de la notice
20/08/2019 15:27
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