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      An unusual cause of infant’s stridor – congenital laryngocele

      case-report

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          Abstract

          Congenital laryngocele is an uncommon cause of neonatal stridor. There are only a few cases reported in the literature. The authors present a successfully treated case of an infant, whose life could only be saved by urgent tracheostomy. On the 5th postoperative day endoscopic excision and marsupialization provided patent airway. The patient could be decannulated. During follow-up no recurrence was observed.

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          Neonatal laryngoceles. A cause for airway obstruction.

          L. Chu, G S Gussack, J Orr … (1994)
          The neonatal laryngocele is a congenital pathologic entity originating in the saccule of the laryngeal ventricle. This entity may present as an uncommon cause of neonatal airway obstruction. We present two cases of this condition and the management undertaken. Both patients demonstrated significant airway distress. Evaluation of each patient included either plain x-ray films of the neck, ultrasound, or computed tomography of the neck. A cystic mass, containing air and fluid, was identified causing external compression of the airway in each case. Surgical intervention required airway endoscopy and an external approach to excise the mass. Tracheotomy was avoided in both cases; however, one infant required further surgery for laryngomalacia. Both children have done well in follow-up.
          Article 0 comments Cited 3 times – based on 0 reviews     Review now
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            Laryngeal cysts in infants and children—A pathologist's perspective (with review of literature)

            Debarshi Saha, Ruchi Sinha, Radha R Pai … (2013)
            To expose the rarity of the phenomena of congenital laryngeal cysts. Additionally, a discussion is presented in support of the basic similarities between laryngeal duplication cyst and bronchogenic cyst and a proposal to use the term 'bronchogenic cyst' (appended by the location) is put forth.
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              Rotation Technique of Reduction Malar Plasty

              Ji-Woong Choung (2015)
              Abstract The 2 most common complications of reduction malarplasty are nonunion or malunion and cheek drooping. Because masseter muscle is attached from zygomatic process of the maxilla to inferior two thirds of the zygomatic arch, rigid fixation and intimate bone contact without creating a gap are crucial for reduction malarplasty. Mesial-clockwise rotation of the zygomaticomaxillary complex can produce intimate bone contact and facilitates reduction malarplasty.
              Article 0 comments Cited 2 times – based on 0 reviews     Review now
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                Author and article information

                Contributors
                Ambrus Andrea: ambrus.andrea@med.u-szeged.hu
                Journal
                Journal ID (nlm-ta): J Otolaryngol Head Neck Surg
                Journal ID (iso-abbrev): J Otolaryngol Head Neck Surg
                Title: Journal of Otolaryngology - Head & Neck Surgery
                Publisher: BioMed Central (London )
                ISSN (Print): 1916-0208
                ISSN (Electronic): 1916-0216
                Publication date (Electronic): 1 June 2020
                Publication date PMC-release: 1 June 2020
                Publication date Collection: 2020
                Volume: 49
                Electronic Location Identifier: 34
                Affiliations
                [1 ]GRID grid.9008.1, ISNI 0000 0001 1016 9625, Department of Otorhinolaryngology, Head and Neck Surgery, , University of Szeged, ; Szeged, Hungary
                [2 ]GRID grid.11804.3c, ISNI 0000 0001 0942 9821, 1st Department of Paediatrics, , Semmelweis University, ; Budapest, Hungary
                [3 ]Department of Pathology, Budapest, Hungary
                [4 ]Szent Imre University Teaching Hospital, Budapest, Hungary
                Article
                Publisher ID: 430
                DOI: 10.1186/s40463-020-00430-9
                PMC ID: 7268503
                PubMed ID: 32487170
                SO-VID: 941ed1c2-8a14-4d52-a54a-80471fed4b83
                Copyright © © The Author(s) 2020
                License:

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                Date received : 12 December 2018
                Date accepted : 24 May 2020
                Categories
                Subject: Case Report
                Custom metadata
                issue-copyright-statement © The Author(s) 2020

                Keywords: congenital stridor,laryngocele,airway obstruction
                Data availability:
                Keywords: congenital stridor, laryngocele, airway obstruction

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