A rare erosive orbital mass in a child: Case report of myofibroma

Purpose: To present the clinical, histological, and radiographic findings of a case of orbital myofibroma in an unusual location. The literature is reviewed and the clinical relevance discussed. Methods: A 5-year-old boy was examined with a 1.5-month history of progressive swelling in the left supra...

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Main Authors: Bahram Eshraghi, Shima Dehghani, Ghasem Saeedi-Anari
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2017-09-01
Series:Journal of Current Ophthalmology
Online Access:http://www.sciencedirect.com/science/article/pii/S2452232517300045
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spelling doaj-0ff9b5015fe6448ebabce6bffc7dfddf2021-03-02T05:27:47ZengWolters Kluwer Medknow PublicationsJournal of Current Ophthalmology2452-23252017-09-01293224227A rare erosive orbital mass in a child: Case report of myofibromaBahram Eshraghi0Shima Dehghani1Ghasem Saeedi-Anari2Eye Research Center, Farabi Eye Hospital, Tehran University of Medical Sciences, Tehran, IranCorresponding author.; Eye Research Center, Farabi Eye Hospital, Tehran University of Medical Sciences, Tehran, IranEye Research Center, Farabi Eye Hospital, Tehran University of Medical Sciences, Tehran, IranPurpose: To present the clinical, histological, and radiographic findings of a case of orbital myofibroma in an unusual location. The literature is reviewed and the clinical relevance discussed. Methods: A 5-year-old boy was examined with a 1.5-month history of progressive swelling in the left supraorbital region. Results: Examination revealed a firm, painless mass in the supralateral region of the left orbit with slight reddish discoloration of the overlying skin. Computerized tomography (CT) scan images showed a well demarcated, homogenous, solid mass with extension to the lacrimal gland region and adjacent to frontal bone erosion. The mass was surgically excised and was confirmed to be myofibroma in diagnostic histological studies. There has been no evidence of recurrence in the first year after surgery. Conclusions: Clinical appearance and imaging findings are unspecific for this tumor, and histological examination still remains the definite method of diagnosis. Therefore, it is important to be able to differentiate myofibromas from other malignant tumors with a similar presentation in pediatric patients to avoid mismanagement. Keywords: Orbital tumor, Lacrimal gland, Children, Histopathologyhttp://www.sciencedirect.com/science/article/pii/S2452232517300045
collection DOAJ
language English
format Article
sources DOAJ
author Bahram Eshraghi
Shima Dehghani
Ghasem Saeedi-Anari
spellingShingle Bahram Eshraghi
Shima Dehghani
Ghasem Saeedi-Anari
A rare erosive orbital mass in a child: Case report of myofibroma
Journal of Current Ophthalmology
author_facet Bahram Eshraghi
Shima Dehghani
Ghasem Saeedi-Anari
author_sort Bahram Eshraghi
title A rare erosive orbital mass in a child: Case report of myofibroma
title_short A rare erosive orbital mass in a child: Case report of myofibroma
title_full A rare erosive orbital mass in a child: Case report of myofibroma
title_fullStr A rare erosive orbital mass in a child: Case report of myofibroma
title_full_unstemmed A rare erosive orbital mass in a child: Case report of myofibroma
title_sort rare erosive orbital mass in a child: case report of myofibroma
publisher Wolters Kluwer Medknow Publications
series Journal of Current Ophthalmology
issn 2452-2325
publishDate 2017-09-01
description Purpose: To present the clinical, histological, and radiographic findings of a case of orbital myofibroma in an unusual location. The literature is reviewed and the clinical relevance discussed. Methods: A 5-year-old boy was examined with a 1.5-month history of progressive swelling in the left supraorbital region. Results: Examination revealed a firm, painless mass in the supralateral region of the left orbit with slight reddish discoloration of the overlying skin. Computerized tomography (CT) scan images showed a well demarcated, homogenous, solid mass with extension to the lacrimal gland region and adjacent to frontal bone erosion. The mass was surgically excised and was confirmed to be myofibroma in diagnostic histological studies. There has been no evidence of recurrence in the first year after surgery. Conclusions: Clinical appearance and imaging findings are unspecific for this tumor, and histological examination still remains the definite method of diagnosis. Therefore, it is important to be able to differentiate myofibromas from other malignant tumors with a similar presentation in pediatric patients to avoid mismanagement. Keywords: Orbital tumor, Lacrimal gland, Children, Histopathology
url http://www.sciencedirect.com/science/article/pii/S2452232517300045
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