Bulletin of Stomatology and Maxillofacial Surgery
ISSN 1829-006X
2025; 234–238
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CONGENITAL NASAL GROWTH IN A NEWBORN:A CASE REPORT ON DIAGNOSIS AND SURGICAL MANAGEMENT

Narek Mkrtchyan*, Grigor Khachatryan, Ani Asatryan

Department of Surgical Stomatology and Maxillofacial Surgery, Yerevan State Medical University after Mkhitar Heratsi Clinic of Pediatric Maxillofacial Surgery and ENT, Muratsan University Hospital Complex,Yerevan, Armenia · Clinic of Pediatric Maxillofacial Surgery and ENT, Muratsan University Hospital Complex, Yerevan, Armenia

Received: 2026-04-08 · Published: 2025-05-25

© 2025 The Author(s) and the original publisher.

CC BY-NC 4.0 This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
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Original title
CONGENITAL NASAL GROWTH IN A NEWBORN:A CASE REPORT ON DIAGNOSIS AND SURGICAL MANAGEMENT
Authors
Narek Mkrtchyan, Grigor Khachatryan, Ani Asatryan
Source journal
Bulletin of Stomatology and Maxillofacial Surgery
Published
2025-05-25
Licence
Creative Commons Attribution-NonCommercial 4.0 International
Original
https://doi.org/10.58240/1829006X-2025.21.4-234

Abstract

Background: Congenital nasal masses, although rare, pose significant clinical challenges, particularly in neonates. These masses may be benign or malignant, and careful monitoring and early intervention are essential to avoid complications. This case report describes a male neonate with a congenital growth at the tip of his nose. Material and Methods: We report the case of a 1,5-year-old child who were treated for nasal growth in our unit, inclusive, were reviewed retrospectively. Information recorded included medical history, clinical characteristics, diagnostic procedures, treatment methods, and the outcome. Results: At six months mass was removed under general anesthesia without complication. This case highlights the importance of early diagnosis and timely surgical treatment for congenital nasal masses, ensuring both functional and cosmetic benefits. Conclusion: Congenital nasal masses, though rare, require careful monitoring and timely intervention to prevent complications.
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