Characteristic findings in the human fetus vestibule: A human temporal bone study.

Collapse Endolymph-perilymph border Human fetuses Membranous labyrinth Perilymphatic space Vestibule

Journal

Auris, nasus, larynx
ISSN: 1879-1476
Titre abrégé: Auris Nasus Larynx
Pays: Netherlands
ID NLM: 7708170

Informations de publication

Date de publication:
Feb 2024
Historique:
received: 04 02 2023
revised: 16 05 2023
accepted: 22 05 2023
pubmed: 13 6 2023
medline: 13 6 2023
entrez: 12 6 2023
Statut: ppublish

Résumé

The "collapse," a highly flexed, dented, or caved membrane between the endo- and peri-lymph of the saccule and utricle in adults, is considered as a morphological aspect of Ménière's syndrome. Likewise, when mesh-like tissues in the perilymphatic space are damaged or lost, the endothelium loses mechanical support and causes nerve irritation. However, these morphologies were not examined in fetuses. By using histological sections from 25 human fetuses (crown-rump length[CRL] 82-372 mm; approximately 12-40 weeks), morphologies of the perilymphatic-endolymphatic border membrane and the mesh-like tissue around the endothelium were examined. The highly flexed or caved membrane between the endo- and peri-lymphatic spaces was usually seen in the growing saccule and utricle of fetuses, especially at junctions between the utricle and ampulla at midterm. Likewise, the perilymphatic space around the saccule, utricle and semicircular ducts often lost the mesh-like tissues. The residual mesh-like tissue supported the veins, especially in the semicircular canal. Within a cartilaginous or bony room showing a limited growth in size but containing increased perilymph, the growing endothelium appeared to become wavy. Owing to a difference in growth rates between the utricle and semicircular duct, the dentation tended to be more frequently seen at junctions than at free margins of the utricle. The difference in site and gestational age suggested that the deformity was not "pathological" but occurred due to unbalanced growth of the border membrane. Nevertheless, the possibility that the deformed membrane in fetuses was an artifact caused by delayed fixation is not deniable.

Identifiants

pubmed: 37308374
pii: S0385-8146(23)00100-1
doi: 10.1016/j.anl.2023.05.004
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

147-153

Informations de copyright

Copyright © 2023. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare no conflict of interest.

Auteurs

Yohei Honkura (Y)

Department of Otolaryngology-Head and Neck Surgery, Tohoku University Graduate School of Medicine, 1-1 Seiryo-machi, Aoba, Sendai 980-8574, Japan. Electronic address: y-honkura@orl.med.tohoku.ac.jp.

Yukio Katori (Y)

Department of Otolaryngology-Head and Neck Surgery, Tohoku University Graduate School of Medicine, 1-1 Seiryo-machi, Aoba, Sendai 980-8574, Japan.

Ai Hirano-Kawamoto (A)

Department of Otolaryngology-Head and Neck Surgery, Tohoku University Graduate School of Medicine, 1-1 Seiryo-machi, Aoba, Sendai 980-8574, Japan.

Tetsuaki Kawase (T)

Department of Otolaryngology-Head and Neck Surgery, Tohoku University Graduate School of Medicine, 1-1 Seiryo-machi, Aoba, Sendai 980-8574, Japan.

Jose Francisco Rodríguez-Vázquez (JF)

Department of Anatomy and Human Embryology, Institute of Embryology, Complutense University, Madrid, Spain.

Gen Murakami (G)

Division of Internal Medicine, Cupid Clinic, Iwamizawa, Japan.

Hiroshi Abe (H)

Emeritus professor of Akita University School of Medicine, Akita, Japan.

Classifications MeSH