A Neonatal Case of Glial Choristoma of the Tongue Causing Airway Obstruction

Glial choristoma is considered to be a type of brain heterotopia consisting of ectopic central nervous tissue. We herein report a neonate with glial choristoma of the tongue who developed respiratory distress due to airway obstruction. A male neonate presented with respiratory distress due to a soft...

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Main Authors: Hajime Machi, Hiroki Karata, Yusuke Yamane, Junya Fukuoka, Yasutomo Funakoshi, Hiroyuki Moriuchi
Format: Article
Language:English
Published: Hindawi Limited 2017-01-01
Series:Case Reports in Otolaryngology
Online Access:http://dx.doi.org/10.1155/2017/2413035
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spelling doaj-762d81f15e8140328edddfe5ff33a8562020-11-25T00:08:12ZengHindawi LimitedCase Reports in Otolaryngology2090-67652090-67732017-01-01201710.1155/2017/24130352413035A Neonatal Case of Glial Choristoma of the Tongue Causing Airway ObstructionHajime Machi0Hiroki Karata1Yusuke Yamane2Junya Fukuoka3Yasutomo Funakoshi4Hiroyuki Moriuchi5Department of Pediatrics, Nagasaki University Hospital, 1-7-1 Sakamoto, Nagasaki, JapanDepartment of Pathology, Nagasaki University Hospital, 1-7-1 Sakamoto, Nagasaki, JapanDepartment of Pediatric Surgery, Nagasaki University Hospital, 1-7-1 Sakamoto, Nagasaki, JapanDepartment of Pathology, Nagasaki University Hospital, 1-7-1 Sakamoto, Nagasaki, JapanDepartment of Pediatrics, Nagasaki University Hospital, 1-7-1 Sakamoto, Nagasaki, JapanDepartment of Pediatrics, Nagasaki University Hospital, 1-7-1 Sakamoto, Nagasaki, JapanGlial choristoma is considered to be a type of brain heterotopia consisting of ectopic central nervous tissue. We herein report a neonate with glial choristoma of the tongue who developed respiratory distress due to airway obstruction. A male neonate presented with respiratory distress due to a soft mass on the midline region of the dorsal tongue base at birth. He was intubated using a flexible fiberoptic nasopharyngoscope. MRI showed a well-circumscribed mass measuring 25 × 23 × 27 mm in size in the same region. A histologic examination confirmed a pathological diagnosis of glial choristoma. He underwent tracheotomy at 22 days of age, and a subtotal resection of the tumor was performed at five months of age. The clinical behavior of oral glial choristoma varies depending on the age at onset as well as the location and size of the mass. The small size of the organ and the narrow operating field hamper the surgical approach in neonates. The optimal therapeutic strategy for neonatal cases of glial choristoma should thus be determined based on the condition of each individual patient.http://dx.doi.org/10.1155/2017/2413035
collection DOAJ
language English
format Article
sources DOAJ
author Hajime Machi
Hiroki Karata
Yusuke Yamane
Junya Fukuoka
Yasutomo Funakoshi
Hiroyuki Moriuchi
spellingShingle Hajime Machi
Hiroki Karata
Yusuke Yamane
Junya Fukuoka
Yasutomo Funakoshi
Hiroyuki Moriuchi
A Neonatal Case of Glial Choristoma of the Tongue Causing Airway Obstruction
Case Reports in Otolaryngology
author_facet Hajime Machi
Hiroki Karata
Yusuke Yamane
Junya Fukuoka
Yasutomo Funakoshi
Hiroyuki Moriuchi
author_sort Hajime Machi
title A Neonatal Case of Glial Choristoma of the Tongue Causing Airway Obstruction
title_short A Neonatal Case of Glial Choristoma of the Tongue Causing Airway Obstruction
title_full A Neonatal Case of Glial Choristoma of the Tongue Causing Airway Obstruction
title_fullStr A Neonatal Case of Glial Choristoma of the Tongue Causing Airway Obstruction
title_full_unstemmed A Neonatal Case of Glial Choristoma of the Tongue Causing Airway Obstruction
title_sort neonatal case of glial choristoma of the tongue causing airway obstruction
publisher Hindawi Limited
series Case Reports in Otolaryngology
issn 2090-6765
2090-6773
publishDate 2017-01-01
description Glial choristoma is considered to be a type of brain heterotopia consisting of ectopic central nervous tissue. We herein report a neonate with glial choristoma of the tongue who developed respiratory distress due to airway obstruction. A male neonate presented with respiratory distress due to a soft mass on the midline region of the dorsal tongue base at birth. He was intubated using a flexible fiberoptic nasopharyngoscope. MRI showed a well-circumscribed mass measuring 25 × 23 × 27 mm in size in the same region. A histologic examination confirmed a pathological diagnosis of glial choristoma. He underwent tracheotomy at 22 days of age, and a subtotal resection of the tumor was performed at five months of age. The clinical behavior of oral glial choristoma varies depending on the age at onset as well as the location and size of the mass. The small size of the organ and the narrow operating field hamper the surgical approach in neonates. The optimal therapeutic strategy for neonatal cases of glial choristoma should thus be determined based on the condition of each individual patient.
url http://dx.doi.org/10.1155/2017/2413035
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