Literature DB >> 15167741

Involvement of the bony orbit in infantile myofibromatosis.

Antonio Augusto V Cruz1, Elizabeth M Maia, Tiana G Burmamm, Luiz C Perez, Andreia N Santos, Elvis T Valera, Luis G Tone.   

Abstract

Infantile myofibromatosis is a rare disorder of infancy that can provoke osteolytic lesions. A 15-day-old infant presented with three round, firm lesions located on the forehead, shoulder, and back. Excisional biopsy of the forehead lesion revealed that the tumor was composed of spindle cells resembling normal smooth muscle arranged in short fascicles. Immunohistochemical staining was positive for vimentin and actin. Five months later, the child presented with three new lesions, including one in the superolateral aspect of the left orbit. It is important to recognize the multicentric form of infantile myofibromatosis because, despite its aggressive clinical presentation, the disease is benign and usually does not require extensive surgery or chemotherapy.

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Year:  2004        PMID: 15167741     DOI: 10.1097/01.iop.0000123501.30336.2c

Source DB:  PubMed          Journal:  Ophthalmic Plast Reconstr Surg        ISSN: 0740-9303            Impact factor:   1.746


  4 in total

Review 1.  Orbital infantile myofibroma: a case report and clinicopathologic review of 24 cases from the literature.

Authors:  Corey J Mynatt; Kenneth A Feldman; Lester D R Thompson
Journal:  Head Neck Pathol       Date:  2011-04-22

2.  Solitary orbital myofibroma in a child: A rare case report with literature review.

Authors:  Bejjanki Kavya Madhuri; Devjyoti Tripathy; Ruchi Mittal
Journal:  Indian J Ophthalmol       Date:  2019-07       Impact factor: 1.848

3.  Primary Resection and Immediate Autologous Reconstruction of Fronto-orbital Infantile Myofibromatoses.

Authors:  Jennifer L Lavie; Camille L Rogers; Mark W Stalder; Hugo St Hilaire
Journal:  Plast Reconstr Surg Glob Open       Date:  2021-01-22

4.  Solitary adult orbital myofibroma: Report of a case and review of the literature.

Authors:  Nicole C Morrow; Munir R Tanas; Nasreen A Syed; Anand Rajan Kd
Journal:  Am J Ophthalmol Case Rep       Date:  2020-10-09
  4 in total

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