SHERP

Tracheal atresia: A Case Report

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Authors
Chi, Je G.; Shong, Young K.; Kim, Chul Woo
Issue Date
1983-03
Publisher
서울대학교 의과대학
Citation
Seoul J Med 1983;24(1):152-155
Abstract
A rare congenital anomaly, tracheal atresia
associated with multisystemic malformation is
reported. The larynx was developed normally
and just below the vocal cord the tracheal lumen
was completely occluded. The larynx was connected
to the distal trachea by a thin fibrocartilagenous
cord that was considered to be a tracheal
remnant.
The two main bronchi were fused at the
canna. No tracheoesophageal fistula was present.
The embryonic basis of this anomaly is briefly
reviewed. In view of the associated multisystemic
malformation, the pathogenesis is presumed
to be an insult in a critical embryonic stage,
Language
English
URI
http://hdl.handle.net/10371/6702
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College of Medicine/School of Medicine (의과대학/대학원)Dept. of Medicine (의학과)The Seoul Journal of MedicineThe Seoul Journal of Medicine Vol. 24 No.1 (1983)
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