Periorbital Myofibroma in a Child: A Case Report and Review of the Literature.


Journal

Ophthalmic plastic and reconstructive surgery
ISSN: 1537-2677
Titre abrégé: Ophthalmic Plast Reconstr Surg
Pays: United States
ID NLM: 8508431

Informations de publication

Date de publication:
Historique:
pubmed: 7 4 2020
medline: 19 3 2021
entrez: 7 4 2020
Statut: ppublish

Résumé

Infantile myofibroma is a rare benign tumor usually diagnosed before the age of 2 and found in the head and neck but much more rarely in the orbital region. There have only been 7 cases of periorbital myofibromas reported in children in the literature to date. The current case is of an 8-year-old boy with a left upper eyelid myofibroma confirmed on histopathological and immunochemical analysis. A literature review of periorbital myofibromas has been performed to bring the reader up-to-date with the current understanding and management of the disease.

Identifiants

pubmed: 32251175
doi: 10.1097/IOP.0000000000001632
pii: 00002341-202009000-00037
doi:

Types de publication

Case Reports Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

e127-e128

Références

Stout AP. Juvenile fibromatoses. Cancer 1954;7:953–978.
Hicks J, Mierau G. The spectrum of pediatric fibroblastic and myofibroblastictumors. Ultrastruct Pathol 2004;28:265–281.
Eyden B. Electron microscopy in the study of myofibroblastic lesions. Semin Diagn Pathol 2003;20:13–24.
Linder JS, Harris GJ, Segura AD. Periorbital infantile myofibromatosis. Arch Ophthalmol 1996;114:219–222.
Bayramlar H, Hepsen IF, Saraç K, et al. Periorbital solitary-type infantile myofibromatosis. J Pediatr Ophthalmol Strabismus 1997;34:63–65.
Westfall AC, Mansoor A, Sullivan SA, et al. Orbital and periorbital myofibromas in childhood: two case reports. Ophthalmology 2003;110:2000–2005.
Friis J, Daugaard S, Heegaard S, et al. Solitary myofibroma of the eyelid. Acta Ophthalmol Scand 2004;82:109–111.
AsadiAmoli F, Sina AH, Kasai A, Ayan Z. A well-known lesion in an unusual location: infantile myofibroma of the eyelid: a case report and review of literature. Acta Med Iran 2010;48:412–416.
Gatibelza ME, Vazquez BR, Bereni N, et al. Isolated infantile myofibromatosis of the upper eyelid: uncommon localization and long-term results after surgical management. J Pediatr Surg 2012;47:1457–1479.
MacIntosh PW, Grob SR, Stagner AM, et al. Multicentric myofibromatosis presenting as a large congenital eyelid myofibroma. J AAPOS 2016;20:70–73.
Chung EB, Enzinger FM. Infantile myofibromatosis. Cancer 1981;48:1807–1818.
Beck JC, Devaney KO, Weatherly RA, et al. Pediatric myofibromatosis of the head and neck. Arch Otolaryngol Head Neck Surg 1999;125:39–44.

Auteurs

Benjamin Sim (B)

Sydney Eye Hospital.

Andrew Gal (A)

Laverty Pathology.

Krishna Tumuluri (K)

Westmead Hospital.
The Children's Hospital at Westmead, Sydney, Australia.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH