ISSN: 2960-1959
Publisher
Case Reports

Infraorbital Myofibroma of Infra-orbital Region: A Rare Case Report

Smart Health Tower, Madam Mittrand, Sulaimani, Kurdistan, Iraq
Smart Health Tower, Madam Mittrand, Sulaimani, Kurdistan, Iraq
Smart Health Tower, Madam Mittrand, Sulaimani, Kurdistan, Iraq
Smart Health Tower, Madam Mittrand, Sulaimani, Kurdistan, Iraq
Smart Health Tower, Madam Mittrand, Sulaimani, Kurdistan, Iraq
Smart Health Tower, Madam Mittrand, Sulaimani, Kurdistan, Iraq
University of Suliamni
College of Medicine, University of Sulaimani, Sulaimani, Kurdistan, Iraq
Research Center, University of Halabja, Halabja, Kurdistan, Iraq
Smart Health Tower, Madam Mittrand, Sulaimani, Kurdistan, Iraq

Abstract

Introduction

Infantile myofibroma is a rare tumor of myofibroblastic origin that can affect soft tissue, bones, or internal organs. The aim of the current study is to report a rare case of a solitary infra-orbital infantile myofibroma.

Case presentation

An 11-month-girl presented with progressive swelling of the left infra-ocular region for two weeks. On examination, there was a well-defined swelling with a localized border that was firm, non-mobile, tender, fixed to the underlying bone, and non-adherent to the superficial skin. Under general anesthesia, the right infraorbital mass was excised. The wound was closed by layers, and the histopathological examination revealed a 3 cm myofibroblastic mass that invaded the margins at multiple spots.

Conclusion

Infraorbital myofibroma is an extremely rare type of myofibroma. Excision with primary closure is the definitive management therapy.

References

  1. Venkatesh V, Kumar BP, Kumar KA, Mohan AP. Myofibroma-a rare entity with unique clinical presentation. J Maxillofac Oral Surg. 2015;14(Suppl 1):64-8. doi:10.1007/s12663-011-0299-5
  2. Amoli FA, 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 Medica Iranica. 2010:412-6. doi:N/A
  3. Mynatt CJ, Feldman KA, Thompson LD. Orbital infantile myofibroma: a case report and clinicopathologic review of 24 cases from the literature. Head Neck Pathol. 2011;5(3):205-15. doi:10.1007/s12105-011-0260-4
  4. Aso S. Muhialdeen, Jaafar Omer Ahmed, Hiwa O. Baba, Ismael Y. Abdullah, Hemn Ali Hassan, Kayhan A. Najar, et al. Kscien’s List; A New Strategy to Discourage Predatory Journals and Publishers (Second Version). Barw Medical Journal. 2023;1(1). doi: 10.58742/bmj.v1i1.14.
  5. Wolfe III JT, Cooper PH. Solitary cutaneous “infantile” myofibroma in a 49-year-old woman. Human pathology. 1990;21(5):562-4. doi:10.1016/0046-8177(90)90015-w
  6. Eze N, Pitkin L, Crowley S, Wilson P, Daya H. Solitary infantile myofibroma compromising the airway. International journal of pediatric otorhinolaryngology.2004;68(12):1533-7. doi:10.1016/j.ijporl.2004.04.035
  7. Ivanov A, Valyi-Nagy T, Nikas D. Extracalvarial Composite Infantile Myofibromatosis: Case Report and Literature Review. European Journal of Pediatric Surgery Reports. 2016;4(01):022-5. doi:10.1055/s-0036-1580704
  8. Nirvikalpa N, Narayanan V. Intraosseous infantile myofibroma of the mandible. Annals of Maxillofacial Surgery. 2011;1(1):87. doi:10.4103/2231-0746.83151
  9. Thennavan A, Narayanaswamy V, Niazi TM, Rao L, Radhakrishnan R. Infantile myofibroma eroding into the frontal bone: a case report and review of its histopathologic differential diagnosis. Case Reports in Pediatrics. 2012;2012. doi:10.1155/2012/630804

Send mail to Author


Send Cancel
Themes by Openjournaltheme.com