Document Detail


Inflammatory myofibroblastic tumour of the orbit in a 7-year-old child.
MedLine Citation:
PMID:  17362459     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Inflammatory myofibroblastic tumour (IMT) is a rare low-grade lesion in the spectrum of myofibroblastic tumours. Systemic IMT is a well-described entity, but orbital IMT is extremely uncommon. These tumours are detected incidentally or through site-specific complaints. Their presentation may clinically and radiologically mimic that of a malignant neoplasm, thus necessitating a biopsy. Even with reports of persistence, local recurrence and malignant transformation the overall prognosis remains favourable.
Authors:
Syed M Ahmad; Angelo Tsirbas; Michael Kazim
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Clinical & experimental ophthalmology     Volume:  35     ISSN:  1442-6404     ISO Abbreviation:  Clin. Experiment. Ophthalmol.     Publication Date:  2007 Mar 
Date Detail:
Created Date:  2007-03-16     Completed Date:  2007-05-15     Revised Date:  2008-11-21    
Medline Journal Info:
Nlm Unique ID:  100896531     Medline TA:  Clin Experiment Ophthalmol     Country:  Australia    
Other Details:
Languages:  eng     Pagination:  160-2     Citation Subset:  IM    
Affiliation:
Department of Ophthalmology, St Luke's Roosevelt Hospital Center, New York, NY 10025, USA. sma44@columbia.edu
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MeSH Terms
Descriptor/Qualifier:
Biological Markers / analysis
Child
Fibroblasts / chemistry,  pathology*
Humans
Magnetic Resonance Imaging
Male
Muscle, Smooth / chemistry,  pathology*
Orbital Diseases / pathology*
Orbital Pseudotumor / pathology*
Chemical
Reg. No./Substance:
0/Biological Markers

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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