Solitary orbital myofibroma in a child: A rare case report with literature review
نویسندگان
چکیده
منابع مشابه
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 supraorbital region. RESULTS Examination revealed a firm, painless mass in the supralateral region o...
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Purpose: To present a patient with interaconal orbital angioleiomyoma. Case Report: A 22-year-old woman presented with painless slowly progressive proptosis. CT and MRI demonstrated a well-defined Interaconal globe size mass (inferomedially). It was isointense in T1 and T2 weighted and homogenously enhanced by Gadolinium. During the surgery, the tumor was excised via a lateral orbitotomy approa...
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Medulloblastoma is quite uncommon in the adult population and even rarer in extra-axial site in cerebello- pontine (CP) angle. In this report, a 23-year-old male patient with a two month history of deafness, nausea, vomiting and ataxia is presented. Clinical and radiological findings demonstrated a heterogeneously enhanced extra-axial lesion in the right CP angle. Total excision was perform...
متن کاملOrbital infantile myofibroma: a case report and clinicopathologic review of 24 cases from the literature.
Isolated orbital infantile myofibroma are rare tumors in the head and neck. The mass-like clinical presentation and variable histologic features result in frequent misdiagnosis and potentially inappropriate clinical management. There are only a few reported cases in the English literature. Twenty-four patients with orbital infantile myofibroma or myofibromatosis were compiled from the English l...
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Myofibroma is a rare benign spindle cell neoplasm in children that usually affects both soft tissue and bone in the head and neck region. Approximately one third of these cases are seen within jaw bones as solitary lesions. Solitary intra-osseous myofibroma of the jaw bone shares its clinical, radiographic and histological features with other spindle cell tumors. The rarity of this lesion can m...
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ژورنال
عنوان ژورنال: Indian Journal of Ophthalmology
سال: 2019
ISSN: 0301-4738
DOI: 10.4103/ijo.ijo_1553_18