Literature DB >> 2147094

Histologic study of eustachian tube cartilage with and without congenital anomalies: a preliminary study.

N Yamaguchi1, I Sando, Y Hashida, H Takahashi, S Matsune.   

Abstract

We investigated histopathologically the development of the eustachian tube (ET) cartilage at a cellular level in individuals with and without congenital anomalies. Fourteen specimens were obtained from 14 individuals ranging in age from 24 weeks' gestation to 3 years who had cleft palate or trisomy 21 (Down) syndrome; the 49 specimens in the nonanomaly (control) group were from 49 individuals ranging from 26 weeks' gestation to 85 years of age. All temporal bone specimens included the ET and its accessory structures, and all were processed and stained with hematoxylin and eosin for histologic study in a routine manner. The number of cartilage cells in the midcartilaginous portion of the ET was determined by light microscopy. In all groups, cartilage cell density of the ET decreased with increasing age. However, cell density tended to be higher at all ages for individuals with cleft palate and microtia versus controls, and tended to be lower at all ages for individuals with Down syndrome.

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Year:  1990        PMID: 2147094     DOI: 10.1177/000348949009901210

Source DB:  PubMed          Journal:  Ann Otol Rhinol Laryngol        ISSN: 0003-4894            Impact factor:   1.547


  4 in total

1.  Long-term otologic status of older cleft palate patients.

Authors:  J A Koempel; A Kumar
Journal:  Indian J Pediatr       Date:  1997 Nov-Dec       Impact factor: 1.967

2.  A comparative evaluation of the Eustachian tube cartilage between healthy and diseased ears using a 3 Tesla MRI.

Authors:  Nevin Aydın; Suzan Saylısoy; Baki Adapınar; Didem Arslantas
Journal:  Pol J Radiol       Date:  2020-10-15

Review 3.  The role of the tensor veli palatini muscle in the development of cleft palate-associated middle ear problems.

Authors:  David S P Heidsieck; Bram J A Smarius; Karin P Q Oomen; Corstiaan C Breugem
Journal:  Clin Oral Investig       Date:  2016-05-07       Impact factor: 3.573

4.  A Novel 12q13.2-q13.3 Microdeletion Syndrome With Combined Features of Diamond Blackfan Anemia, Pierre Robin Sequence and Klippel Feil Deformity.

Authors:  Domenico Roberti; Renata Conforti; Teresa Giugliano; Barbara Brogna; Immacolata Tartaglione; Maddalena Casale; Giulio Piluso; Silverio Perrotta
Journal:  Front Genet       Date:  2018-11-19       Impact factor: 4.599

  4 in total

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