Title of article
PERIBULBAR COMPLEX CHORISTOMA IN ASSOCIATION WITH IPSILATERAL NASAL HYPOPLASIA and NASOLACRIMAL DUCT OBSTRUCTION
Author/Authors
Tabatabaie, S. Z Eye Research Center - Farabi Eye Hospital - Medical Sciences University of Tehran , Rajabi, M. T Eye Research Center - Farabi Eye Hospital - Medical Sciences University of Tehran , Asadi-Amoli, F Eye Research Center - Farabi Eye Hospital - Medical Sciences University of Tehran , Sadeghi-Tari, A Eye Research Center - Farabi Eye Hospital - Medical Sciences University of Tehran , Kasai, A Eye Research Center - Farabi Eye Hospital - Medical Sciences University of Tehran
Pages
4
From page
79
To page
82
Abstract
Developmental midline perinasal masses in children are rare lesions, specifically in
association with choristomas. We encountered a 3-year-old boy with epiphora, a striking mass on the
nasal bridge and ipsilateral nasal hypoplasia. CT scan imaging showed multiple calcified areas within
the tumor in addition to linear defect in frontal bone, hypoplastic left ethmoidal sinus and left nasal
cavity, and absence of left nasal concha. The patient had no history of seizure, no neurologic deficit,
and ocular developmental examinations were normal. After performing excisional biopsy of the tumor,
histopathologic analysis revealed complex choristoma composed of cartilage and bone. The most
appropriate name for this malformation, which to our knowledge has not been described in the
literature, seems to be, nasal hypoplasia with complex choristoma and nasolacrimal duct obstruction.
Keywords
Complex choristoma , nasal hypoplasia , nasolacrimal duct obstruction
Journal title
Astroparticle Physics
Serial Year
2007
Record number
2445129
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