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Author
Masui, Masanori Department of Oral and Maxillofacial Surgery, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Sakamoto, Yumi Department of Oral and Maxillofacial Surgery, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Kunisada, Yuki Department of Oral and Maxillofacial Surgery, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University ORCID Kaken ID researchmap
Ibaragi, Soichiro Department of Oral and Maxillofacial Surgery, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University ORCID Kaken ID publons researchmap
Abstract
Black hairy tongue is a benign condition caused by elongation and defective desquamation of the filiform papillae, and it is uncommon in neonates and infants. We report a case in a 54-day-old girl who presented with a black lesion on the tongue dorsum. The lesion had first been noted at the 1-month medical checkup and persisted despite observation. At presentation, a localized blackish-brown lesion with accentuated filiform papillae was observed on the tongue dorsum and could not be wiped off with gauze. Oral candidiasis was considered in the differential diagnosis, but microbiological examination detected no Candida species. A clinical diagnosis of black hairy tongue was made, and the parents were instructed to gently clean the tongue dorsum with gauze and a sponge brush. The lesion resolved within 2 weeks without recurrence. Recognition of this benign entity may help avoid unnecessary treatment in infants.
Keywords
black hairy tongue
case report
infant
oral hygiene
Published Date
2026-08
Publication Title
Clinical Case Reports
Volume
volume14
Issue
issue8
Publisher
Wiley
Start Page
e73170
ISSN
2050-0904
Content Type
Journal Article
language
English
OAI-PMH Set
岡山大学
File Version
publisher
PubMed ID
DOI
License
http://creativecommons.org/licenses/by/4.0/
Citation
M. Masui, Y. Sakamoto, Y. Kunisada, and S. Ibaragi, “ Black Hairy Tongue in a 54-Day-Old Infant: A Case Report,” Clinical Case Reports 14, no. 8 (2026): e73170, https://doi.org/10.1002/ccr3.73170.