Safety and efficacy of superior turbinate biopsies as a source of olfactory epithelium appropriate for morphological analysis.


Journal

European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery
ISSN: 1434-4726
Titre abrégé: Eur Arch Otorhinolaryngol
Pays: Germany
ID NLM: 9002937

Informations de publication

Date de publication:
Feb 2020
Historique:
received: 30 07 2019
accepted: 07 11 2019
pubmed: 18 11 2019
medline: 8 1 2021
entrez: 18 11 2019
Statut: ppublish

Résumé

There is no standardized approach for preserving olfactory function in the side of the nose where biopsy of the olfactory epithelium (OE) is performed. Moreover, a gold standard technique for obtaining human OE in vivo is still lacking. We determined the efficacy of obtaining good-quality OE specimens suitable for pathological analysis from the lower half of the superior turbinate and verified the safety of this procedure in maintaining bilateral and unilateral olfactory function. In 21 individuals without olfactory complaints and who had undergone septoplasty and inferior turbinectomy OE biopsy was made during septoplasty. Olfactory function, both unilateral and bilateral, was assessed using the University of Pennsylvania Smell Identification Test (UPSIT) before and 1 month after the procedure. Specimens were marked with the olfactory marker protein for confirmation of OE presence. Ninety percent of the samples contained OE, although clear histological characterization was possible from only 62%. There was no deterioration of UPSIT scores either bilaterally or unilaterally on the side of the biopsy. Patients also maintained the ability to identify individual odorants. Biopsies of the lower half of the superior turbinate do not affect olfactory function and show strong efficacy in yielding OE tissue and moderate efficacy for yielding tissue appropriate for morphological analysis. Future studies are needed to assess the safety of this procedure in other OE regions.

Identifiants

pubmed: 31734722
doi: 10.1007/s00405-019-05728-7
pii: 10.1007/s00405-019-05728-7
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

483-492

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Auteurs

Ellen Cristine Duarte Garcia (ECD)

Department of Clinical Surgery, Londrina State University (UEL), Londrina, PR, Brazil.

Ana Carolina Rossaneis (AC)

Laboratory of Pain, Inflammation, Neuropathy and Cancer, Department of Pathological Sciences, UEL, Londrina, PR, Brazil.

Alexandre Salvatore Pipino (AS)

Department of Clinical Surgery, Londrina State University (UEL), Londrina, PR, Brazil.

Gustavo Vasconcelos Gomes (GV)

Department of Clinical Surgery, Londrina State University (UEL), Londrina, PR, Brazil.

Fábio de Rezende Pinna (F)

Department of Otorhinolaryngology, University of São Paulo, São Paulo, SP, Brazil.

Richard Louis Voegels (RL)

Department of Otorhinolaryngology, University of São Paulo, São Paulo, SP, Brazil.

Richard L Doty (RL)

Smell and Taste Center, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Waldiceu Aparecido Verri (WA)

Laboratory of Pain, Inflammation, Neuropathy and Cancer, Department of Pathological Sciences, UEL, Londrina, PR, Brazil.

Marco Aurélio Fornazieri (MA)

Department of Clinical Surgery, Londrina State University (UEL), Londrina, PR, Brazil. marcofornazieri@gmail.com.
Department of Otorhinolaryngology, University of São Paulo, São Paulo, SP, Brazil. marcofornazieri@gmail.com.
Department of Medicine, Pontifical Catholic University of Paraná, Londrina, Brazil. marcofornazieri@gmail.com.

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