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Journal articles on the topic 'Laryngocele'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

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1

Mobashir, Mohammad Kamal, Waleed M. Basha, Abd ElRaof Said Mohamed, Mostafa Hassaan, and Ahmed M. Anany. "Laryngoceles: Concepts of Diagnosis and Management." Ear, Nose & Throat Journal 96, no. 3 (2017): 133–38. http://dx.doi.org/10.1177/014556131709600313.

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A laryngocele is an abnormal dilatation of the laryngeal saccule. It is a rare benign lesion of the larynx. Various modalities of treatment have been advocated for its management. We present our treatment results and outcomes of a series of cases of laryngoceles and discuss the concepts of their management. This study included patients with different laryngocele types. Patients with an internal laryngocele underwent endoscopic CO2 laser resection, while those with a combined laryngocele underwent resection via a V-shaped lateral thyrotomy approach. Seven patients had an internal laryngocele, a

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Verro, Barbara, and Carmelo Saraniti. "CO2 Laser Marsupialization for Internal and Combined Laryngocele." International Archives of Otorhinolaryngology 27, no. 03 (2023): e428-e434. http://dx.doi.org/10.1055/s-0042-1748926.

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Abstract Introduction Laryngocele is an air-filled dilatation of the laryngeal saccule that can be classified according to its extent (internal, external, or combined) and contents (laryngocele or laryngopyocele). To date, there is no consensus on the best treatment for laryngocele. Objective The present study aims to demonstrate for the first time the effectiveness of CO2 laser marsupialization for internal and combined laryngoceles. Methods A retrospective study was accomplished in our ENT Clinic of the University Hospital, from 2010 to today, recruiting patients according to strict criteria

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3

Abdelilah, Arioua, Afellah Mohamed, Bouhlala Anouar, et al. "Laryngomucocele: A Case Report and Literature Review." SAS Journal of Surgery 10, no. 04 (2024): 413–18. http://dx.doi.org/10.36347/sasjs.2024.v10i04.003.

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Laryngocele is a rare benign affection characterized by the abnormal dilatation of the laryngeal saccule or Morganii ventricle. Laryngocele can be classified as internal, external and mixed (both). Many laryngoceles are asymptomatic; Sometimes it is presented as cervical swelling causing airway obstruction in need of emergency intervention. Computed tomography scan is the most effective imaging method for diagnosis. Surgery is the treatment of choice. We are reporting a case of laryngocele in 50-year-old male, who presented a recent dysphonia and solid dysphagia, along with an anterior cervica

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Zelenik, Karol, Lucia Stanikova, Katarina Smatanova, Michal Cerny, and Pavel Kominek. "Treatment of Laryngoceles: What Is the Progress over the Last Two Decades?" BioMed Research International 2014 (2014): 1–6. http://dx.doi.org/10.1155/2014/819453.

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Objectives. To review surgical techniques used in the treatment of laryngoceles over the last two decades and point out developments and trends.Materials and Methods. PubMed, the Cochrane Library, and the JBI Library of Systematic Reviews were searched using the term “laryngocele.” Demographic data, type of laryngocele, presence of a laryngopyocele, type of treatment and need for a tracheotomy were assessed.Results. Overall, data on 86 patients were analyzed, culled from 50 articles, of which 41 were case reports and 9 were case series. No single systematic review or meta-analysis or randomize

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Murray, Sean P., Lawrence P. A. Burgess, Deborah Mitchell Burton, Carlos Gonzalez, Gordon S. Wood, and Joan T. Zajtchuk. "Laryngocele Associated with Squamous Carcinoma in a 20-Year-Old Nonsmoker." Ear, Nose & Throat Journal 73, no. 4 (1994): 258–61. http://dx.doi.org/10.1177/014556139407300413.

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A laryngocele associated with squamo us cell carcinoma of the larynx is reported in a 20-yea r-old man without a history of smoking. This is the youngest reported case of carcinoma associated with laryngocele in the literature. This association is supported by the patient's young age and his nonsmoking status. However, this case does not appear to support the conclusion that laryngoceles predispose to the development of squamous cell carcinoma. The clinical history supports the tumor obstruction theory, whereby a laryngocele developed from an obstructing carcinoma of the ventricle.

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Singh, Ravjit, William Karantanis, Matthew Fadhil, Shivani Angelique Kumar, Julia Crawford, and Ian Jacobson. "Systematic review of laryngocele and pyolaryngocele management in the age of robotic surgery." Journal of International Medical Research 48, no. 10 (2020): 030006052094044. http://dx.doi.org/10.1177/0300060520940441.

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Objective A laryngocele is a space that develops as a result of pathological dilatation of the laryngeal saccule. However, the reported management of laryngoceles varies. We conducted a systematic review of the literature regarding the surgical management of laryngoceles and pyolaryngoceles, to understand the evolving nature of treatment for this rare condition. Methods We searched for publications in the PubMed, Cochrane Library, JBI Library of Systematic Reviews, and Ovid databases using the terms “laryngocele”, “pyolaryngocele”, and “laryngopyocele”, and reviewed the identified articles. Re

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7

Close, Lanny Garth, Marie Merkel, Dennis K. Burns, C. William Deaton, and Steven D. Schaefer. "Asymptomatic Laryngocele: Incidence and Association with Laryngeal Cancer." Annals of Otology, Rhinology & Laryngology 96, no. 4 (1987): 393–99. http://dx.doi.org/10.1177/000348948709600409.

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Since laryngoceles are usually asymptomatic, their incidence is probably higher than the literature suggests. With the advent of computed tomography, the incidence and significance of the asymptomatic laryngocele in a general head and neck practice can be addressed. To this end, 304 consecutive patients with a variety of otolaryngic diagnoses were studied prospectively by computed tomography of the neck from January 1983 to February 1985. Thirty-eight (12.5%) of the patients had asymptomatic laryngoceles, defined as air-containing structures in the supraglottic region extending more than 5 mm

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8

Myssiorek, David, and Mark Persky. "Laser Endoscopic Treatment of Laryngoceles and Laryngeal Cysts." Otolaryngology–Head and Neck Surgery 100, no. 6 (1989): 538–41. http://dx.doi.org/10.1177/019459988910000602.

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The laryngocele and saccular cyst are uncommon anomalies of the larynx. Two patients, one with an Intemal laryngocele and one with a saccular cyst, were successfully treated by endoscopic laser marsupialization of their lesions. Since neither patient was found to be a suitable candidate for prolonged general anesthesia, the patients did not require a tracheotomy and were discharged the day after surgery. Both patients are doing well, with remarkable Improvement in their voices persisting in their three year follow-up. The signs, symptoms, diagnosis, treatment, and Indications for endoscopic la

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Adekanye, Abiola Grace, Theophilus Ipeh Ugbem, Gbenga Kajogbola, and Aniefon Ntuen Udo Umana. "Laryngopyocele: 10 Years’ Experience in a Tertiary Institution, South-South, Nigeria." Calabar Journal of Health Sciences 4 (February 12, 2021): 84–88. http://dx.doi.org/10.25259/cjhs_32_2020.

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Laryngopyocele is an infected laryngocele: Rarer than laryngocele. An estimated 8% of laryngoceles get infected and become laryngopyocele with features of acute airway obstruction and sepsis with resultant fatality. Laryngocele is more common in Caucasian males population after the 5th decades of life. Mostly acquired though could be congenital. Most are unilateral with no predominance for the left or the right. Recently, laryngocele is categorized into internal or mixed (combined). Laryngopyocele accounted for 0.15% of 1376 ENT surgical procedures done in our operative theatre in a period of

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Al-Ogaili, Zeyad, Gavin Chapeikin, and David Palmer. "Primary Aspergillosis of Bilateral Laryngoceles." Case Reports in Medicine 2014 (2014): 1–3. http://dx.doi.org/10.1155/2014/384271.

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Laryngocele is an abnormal dilatation of the saccule of laryngeal ventricle, which is usually unilateral and filled with air or fluid. We present a case of bilateral laryngoceles colonized byAspergillusspecies.

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Ingrams, Duncan, Dominic Hein, and Nicholas Marks. "Laryngocele: an anatomical variant." Journal of Laryngology & Otology 113, no. 7 (1999): 675–77. http://dx.doi.org/10.1017/s0022215100144822.

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AbstractIt is commonly believed that external laryngoceles always penetrate the thyrohyoid membrane at the site of penetration of the neurovascular bundle. We present a case where the site of penetration was posterosuperior to this. Careful dissection of the neck of a laryngocele sac is important to prevent damage to the neurovascular bundle.

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Trivedi, Saurabh, Sunaina Tejpal Karna, Kaushal Singh Baghel, and Pooja Thaware. "Undiagnosed laryngocele: an airway emergency." BMJ Case Reports 15, no. 3 (2022): e248126. http://dx.doi.org/10.1136/bcr-2021-248126.

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Laryngoceles are rare dilated laryngeal saccules that can present as acute airway obstruction and lead to airway emergencies. A man, presented to the emergency room, with difficulty in breathing and change in voice. An unevaluated pulsatile swelling was present on the left side of neck. Since, the patient was in stridor, an awake fiberoptic bronchoscopy (FOB)-guided intubation was planned with readiness for emergency tracheostomy, if needed. On FOB, an edematous supraglottic area with a narrowed glottic opening was observed. The procedure was abandoned and a surgical tracheostomy was performed

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K. U., Raghavendra Prasad, and Sana Aboobaker. "Laryngocele: a case report and review of 50 cases from literature." International Journal of Otorhinolaryngology and Head and Neck Surgery 8, no. 7 (2022): 617. http://dx.doi.org/10.18203/issn.2454-5929.ijohns20221656.

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<p>Laryngocele is a benign dilatation of the laryngeal saccule with incidence of 1 in 2.5 million people per year. Known as a disease of trumpet blowers, laryngocoele mainly affects the older male population with occupational predisposition. We aimed to review a case of laryngocele in a 55-year-old merchant in terms of clinical presentation, radiographical features, other investigations and surgical management. The detailed description of the case of mixed laryngocele which was evaluated in the department of ENT, HIMS, Hassan will be given. Literature was reviewed for similar cases of th

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Spinosi, Maria C., Chiara Mezzedimi, Giovanni Monciatti, and Desiderio Passali. "Internal Laryngocele: Unusual onset in a 91-year-old female patient." Sultan Qaboos University Medical Journal [SQUMJ] 18, no. 1 (2018): 104. http://dx.doi.org/10.18295/squmj.2018.18.01.018.

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While internal laryngoceles rarely cause major clinical complaints, they may lead to airway obstruction and require emergency intervention on rare occasions. We report a 91-year-old patient who was referred to the Ear, Nose & Throat Clinic of the Policlinico Santa Maria alle Scotte, Siena, Italy, in 2017 due to recurrent episodes of severe dyspnoea. A flexible nasopharyngolaryngoscopic examination revealed an internal laryngocele of approximately 1.5 cm in diameter that moved up and down the glottic plane, occasionally invading the subglottic space during inspiration and impeding airflow.

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Olusoga-Peters, Oluwapelumi, Moses Ayodele Akinola, Collins Chijioke Adumah, Babatunde Akinola Bamigboye, and Oluwaseyi Joy Alao. "Congenital laryngocele: An uncommon cause of neonatal respiratory distress." Journal of Case Reports and Images in Otolaryngology 3, no. 2 (2025): 7–11. https://doi.org/10.5348/100007z18op2022cr.

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Introduction: Congenital laryngocele is a rare phenomenon as only a few cases have been reported in literature. It is a pathologic occurrence originating in the saccule of the laryngeal ventricle. In many cases, patients with congenital laryngoceles present with respiratory distress due to the narrow airway of the neonate necessitating urgent surgical management. Case Report: We present a 29-day-old male neonate referred by the pediatrics team of our facility on account of respiratory distress, regurgitation of feeds, and a left-sided neck mass since birth. Evaluation of the patient included n

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Maryam Mohamed Ali, Abdalla Mohamed Etbiga, Maryam Mohamed Ali, Abdalla Mohamed Etbiga. "Mixed Laryngocele: القيلة الحنجرية المختلطة". Journal of medical and pharmaceutical sciences 5, № 2 (2021): 56–50. http://dx.doi.org/10.26389/ajsrp.k100421.

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Laryngocele alludes to dilatation of the saccule of the laryngeal ventricle. It is a rare disease. There are different types, external, internal and mixed. Laryngoceles are more frequently obtained instead of inherent. They are lined by pseudostratified, columnar, ciliated epithelium. Intermittent locales of stratified squamous epithelium (submucosal serous and mucous organs) may be shown. This report describes a 29-year-old Libyan male who had been suffering from left neck swelling for more than 5 years. Over the last months, he had been suffering from the increased size of the swelling but n

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Ettema, Sandra L., Daniel G. Carothers, and Henry T. Hoffman. "Laryngocele Resection by Combined External and Endoscopic Laser Approach." Annals of Otology, Rhinology & Laryngology 112, no. 4 (2003): 361–64. http://dx.doi.org/10.1177/000348940311200411.

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Options in the management of laryngoceles include observation, endoscopic resection, and resection via an external approach. We introduce a combined endoscopic and external approach that we have employed on several occasions to ensure complete removal of the laryngocele and the saccule from which it originated. A case is presented to help define the technique.

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18

Carrat, Xavier, Jean-Marc François, François Devars, Dominique Carles, and Louis Traissac. "Laryngomucocele as an Unusual Late Complication of Subtotal Laryngectomy." Annals of Otology, Rhinology & Laryngology 107, no. 8 (1998): 703–7. http://dx.doi.org/10.1177/000348949810700813.

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We report an unusual case of laryngomucocele occurring after subtotal laryngectomy. Laryngoceles generally have a congenital origin in a long-preexisting saccule, and their association with laryngeal carcinoma is well known. Laryngocele is usually favored by the increase of intraglottic pressure caused by the laryngeal carcinoma. However, an iatrogenic secondary laryngomucocele occurring after a surgical procedure is uncommon. We report in detail the physiopathologic conditions leading to the creation of this lesion.

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19

Zelman, Warren H., and Luke I. Burke. "External Laryngocele: An Unusual Cause of Respiratory Distress in a Newborn." Ear, Nose & Throat Journal 73, no. 1 (1994): 19–22. http://dx.doi.org/10.1177/014556139407300106.

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Congenital larygoceles are rare causes of respiratory distress in the newborn. We report a case of airway compromise in a two day old newborn boy secondary to a solitary giant external laryngocele. No internal component or other laryngeal pathology was found. The patient had a progressively enlarging neck mass and increasing stridor culminating in respiratory arrest. Tracheotomy was avoided and the lesion was excised in its entirety. Airway management, the role of CT scanning, and surgical excision of laryngoceles are discussed.

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Takahara, Miki, Yoshifumi Kobayashi, Yutaka Hayashi, Satoshi Nonaka, Shinichi Kawabori, and Tokuji Unno. "Laryngocele." Koutou (THE LARYNX JAPAN) 8, no. 2 (1996): 155–59. http://dx.doi.org/10.5426/larynx1989.8.2_155.

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Singh, Chirom A., and Pirabu Sakthivel. "Laryngocele." New England Journal of Medicine 379, no. 23 (2018): e40. http://dx.doi.org/10.1056/nejmicm1807310.

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Bonaventurová, Markéta, Jan Plzák, and Michal Zábrodský. "Léčba kombinované laryngokély endoskopickým přístupem – kazuistické sdělení." Otorinolaryngologie a foniatrie 72, no. 4 (2023): 215–20. http://dx.doi.org/10.48095/ccorl2023215.

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Summary Laryngocele is a rare benign disease of the larynx that originates from dilating the laryngeal ventricles. The laryngocele communicates with the laryngeal lumen and so is filled with air. In case of closure, there can be an accumulation of pathological secret presented – mucus (laryngomucocele) and, in case of infection, the pus (laryngopyocele). We distinguish internal or combined laryngocele with the borderline of the thyrohyoid membrane. Clinical features dominate hoarseness, cough, dysphagia, foreign body sensation, and possibly dyspnea or neck mass. It can also be an incidental fi

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Kalsotra, Parmod, Rohan Gupta, Arshad Bhat, KP Singh, and Saurabh Gupta. "Bilateral Mixed Laryngocele." International Journal of Phonosurgery & Laryngology 3, no. 2 (2013): 69–72. http://dx.doi.org/10.5005/jp-journals-10023-1067.

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ABSTRACT Laryngocele is a rare, benign dilatation of the laryngeal saccule that may extend internally into the airway or externally through the thyrohyoid membrane. The incidence of laryngocele is 1 per 2.5 million people per year. It may be asymptomatic or sometimes may present with cough, hoarseness, stridor, sore throat and as a swelling on one or both sides of the neck. We are reporting a case of bilateral mixed laryngocele in a 41 years old male, its clinical presentation and investigations along with a review of literature. How to cite this article Gupta R, Gupta S, Bhat A, Kalsotra P, S

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Gupta, S. C., Arun Goel, and P. A. Singh. "External laryngocele." Indian Journal of Otolaryngology and Head and Neck Surgery 50, no. 3 (1998): 298–301. http://dx.doi.org/10.1007/bf03007015.

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Kohli, G. S., U. Wig, J. K. Sahni, and S. P. S. Yadav. "Traumatic laryngocele." Indian Journal of Otolaryngology 37, no. 3 (1985): 122–23. http://dx.doi.org/10.1007/bf03047656.

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Verret, D. J., Robert J. DeFatta, and Robert Sinard. "Combined Laryngocele." Annals of Otology, Rhinology & Laryngology 113, no. 7 (2004): 594–96. http://dx.doi.org/10.1177/000348940411300715.

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Aydin, Ömer, Emre Üstündaǧ, Mete İşeri, Haluk Özkarakaş, and Ali Oǧuz. "Laryngeal amyloidosis with laryngocele." Journal of Laryngology & Otology 113, no. 4 (1999): 361–63. http://dx.doi.org/10.1017/s0022215100143981.

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AbstractBoth laryngocele and laryngeal amyloidosis are uncommon, and simultaneous occurrences of these entities are extremely rare. A case of laryngeal amyloidosis with laryngocele in which the computed tomography (CT) and magnetic resonance (MR) imaging of the larynx, clearly demonstrating both disease processes, is discussed. Diagnosis is confirmed by histopathologic specimens. Only two cases have been reported in the world literature, and this is the third case of laryngeal amyloidosis associated with laryngocele.

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Ozturk, Kayhan, Cagdas Elsurer, Serap Bulut, Mutlu Duran, and Serdar Ugras. "Cervical Thymic Cyst Mimicking Laryngocele." Case Reports in Otolaryngology 2013 (2013): 1–4. http://dx.doi.org/10.1155/2013/839406.

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Cervical thymic cysts are nearly 0.3% of all congenital cervical cysts. Thymic cysts are asymptomatic, but they rarely complain of dysphagia or tracheal obstruction symptoms. A soft, mobile, and painless mass increasing with valsalva maneuver directs the diagnosis of laryngocele. There has not been any study in the literature in which thymic cyst presenting like laryngocele. We hereby present a case of thymic cyst mimicking laryngocele that has not been reported so far.

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Jovanović, Anđelina, Svetlana Valjarević, and Milan Jovanović. "An unusual case of combined laryngocele presenting as cervical swelling." Medicinska istrazivanja 55, no. 3 (2022): 67–70. http://dx.doi.org/10.5937/medi55-40512.

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Laryngocele is a sac-like, pathological enlargement of the Morgagni's ventricle, which occurs between the true and false vocal cords. This change is filled with air and is continuous with the lumen of the larynx. It is usually asymptomatic and is accidentally detected during radiological diagnostics. We present the case of a 54-year-old patient who came for examination due to a painless swelling in her neck on the left side, which lasted for 8 months and increased upon Valsalva's maneuver. Occasionally the patient was hoarse. By clinical otorhinolaryngological examination and computed tomograp

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Park, Kyung Tae, Youngjin Ahn, Kwang Hyun Kim, and Tack-Kyun Kwon. "Schwannoma Mimicking Laryngocele." Clinical and Experimental Otorhinolaryngology 3, no. 3 (2010): 166. http://dx.doi.org/10.3342/ceo.2010.3.3.166.

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Suqati, Abrar, Ameen Alherabi, Osama Marglani, and Tariq Alaidarous. "Bilateral combined laryngocele." Saudi Medical Journal 37, no. 8 (2016): 902–4. http://dx.doi.org/10.15537/smj.2016.8.15104.

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Palacios, Enrique, and Galdino E. Valvassori. "Mixed (external) Laryngocele." Ear, Nose & Throat Journal 80, no. 9 (2001): 625. http://dx.doi.org/10.1177/014556130108000905.

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Cavo, John W., and Jeffrey C. Lee. "Laryngocele after Childbirthc." Otolaryngology–Head and Neck Surgery 109, no. 4 (1993): 766–68. http://dx.doi.org/10.1177/019459989310900423.

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Ashish, Gaurav. "Venous Ectasia: A Potential Mimicker for Laryngocele Radiology Covers the Road." An International Journal of Otorhinolaryngology Clinics 7, no. 2 (2015): 64–67. http://dx.doi.org/10.5005/jp-journals-10003-1190.

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ABSTRACT Introduction Venous ectasia is rare causes of neck mass. Among neck veins, ectasia of the internal jugular vein (IJV) are extremely uncommon. However, this is to be kept in mind when considering differentials for laryngocele. Objectives To recognize the similarities between laryngocele and ectasias of the IJV and the differences in their presentation and management. Study design Observational. Setting Tertiary care hospital, India. Conclusion Presenting a 7-year-old boy with a left-sided soft, non-tender neck mass that fluctuated in size with coughing and straining for the past 1 year

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Mozumder, Somesh, Shirish Dubey, Aniruddha Dam, and Anup Kumar Bhowmick. "External Laryngocoele or Anterior Jugular Vein Aneurysm (A Rare Clinical Entity): A Paradox Solved by A Few Simple Non-Invasive Radiological Tests." Bengal Journal of Otolaryngology and Head Neck Surgery 26, no. 1 (2018): 73–75. http://dx.doi.org/10.47210/bjohns.2018.v26i1.162.

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Introduction   The differential diagnosis of a cystic upper neck mass that becomes prominent on coughing, straining, breath holding, or Valsalva manoeuvre includes mediastinal tumours and cysts, external laryngeal diverticula, and jugular venous aneurysms. Jugular venous aneurysms, while extremely rare, must be considered. We report the fifth case of anterior jugular aneurysm in an adult patient.  Case Report  A 55 year old female patient presented with a swelling in the upper part of right side of neck near the greater cornu of hyoid bone. The swellin

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SIMIONIUC, Anca, Alina Georgiana ANGHEL, Mihai DUMITRU, Oana Adriana ANGHEL, and Ion ANGHEL. "Left hemilaryngeal carcinoma complicated with an external laryngocele." Romanian Journal of Medical Practice 11, no. 1 (2016): 85–88. http://dx.doi.org/10.37897/rjmp.2016.1.17.

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Laryngocele represents an abnormal invagination of the mucous membrane from the Morgagni laryngeal ventricle, being filled with air and communicating with the laryngeal inlet. The symptoms are intermittent, with recurrent episodes of dysphonia and airway insufficiency. Exceptionally, the wall of the cyst could become malignant. This case was reported given the association between laryngeal carcinoma and external laryngocele.

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Kiricsi, Ágnes, Piroska Fazekas, Attila Nagy, et al. "Laryngokeleeseteink műtéti megoldásai." Orvosi Hetilap 160, no. 31 (2019): 1235–40. http://dx.doi.org/10.1556/650.2019.31447.

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Abstract: Laryngocele is a unilateral or bilateral dilation of the saccule or appendix of the laryngeal ventricle. It is a benign lesion, often without any specific symptom, diagnosed unintentionally, but it can cause life-threatening airway obstruction, needing emergency tracheotomy. The authors present three cases of laryngocele and the related surgical methods. Orv Hetil. 2019; 160(31): 1235–1240.

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Saravanam, Prasanna Kumar, Vinoth Manimaran, Mohamed Ramadhan, and Gowthame Kanagasabai Prakash. "Laryngopyocele in a case of bilateral mixed laryngocele: an impending airway emergency." BMJ Case Reports 12, no. 8 (2019): e229450. http://dx.doi.org/10.1136/bcr-2019-229450.

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Laryngopyocele is a rare complication involving the laryngocele which can present with acute airway compromise. A 31-year-old man presented with acute onset respiratory distress and dysphagia. He had swelling on either side of upper aspect of the neck with tenderness on left side. Videolaryngoscopy using 70° rigid Hopkins rod telescope showed a swelling in the left pyriform sinus pushing the ipsilateral vocal cord. However, glottic space was adequate. Contract-enhanced CT scan of the neck confirmed left-sided mixed laryngopyocele with contralateral mixed laryngocele. Patient underwent excision

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Khan, NA, G. Watson, E. Sivayoham, and DJ Willatt. "Pyolaryngocoele: Management of an Unusual Cause of Odynophagia and Neck Swelling." Clinical medicine. Ear, nose and throat 1 (January 2008): CMENT.S746. http://dx.doi.org/10.4137/cment.s746.

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We present a case of 82 years old female with two-week history of neck swelling, odynophagia, hoarseness and cough. There was a tender, fluctuant swelling below the mandible on right side. An urgent C.T scan showed it to be a pyolaryngocele. High dose intra venous antibiotic, analgesia and nasogastric feeding resolved the acute infective episode. The residual laryngocele was treated by an excision via an external approach. A pyolaryngocele is a rare complication of laryngocele that becomes secondarily infected. It can cause feeding and respiratory compromise because of its compression symptoms

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Berteșteanu, Gabriel V., Alexandru Nicolaescu, Radu C. Popescu, et al. "The laryngocele; case presentation." Journal of Clinical and Investigative Surgery 1, no. 1 (2016): 28–32. http://dx.doi.org/10.25083/2559.5555.11.2832.

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41

B, Umakanth Goud, Hanumantha Rao A V S, Satyanarayana D, Manish Kumar Gupta, and Juveria Majeed. "LARYNGOCELE: A CASE REPORT." Journal of Evolution of Medical and Dental Sciences 4, no. 32 (2015): 5586–91. http://dx.doi.org/10.14260/jemds/2015/817.

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Oukessou, Y., R. L. Abada, M. Roubal, and M. Mahtar. "Laryngocele: An unusual presentation." European Annals of Otorhinolaryngology, Head and Neck Diseases 132, no. 3 (2015): 177–78. http://dx.doi.org/10.1016/j.anorl.2015.03.002.

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Olszewski, J., J. Miłoński, P. Pietkiewicz, and H. Zielińska-Bliźniewska. "RARE CASES OF MIXED LARYNGOCELE." Journal of the Grodno State Medical University 16, no. 3 (2018): 362–65. http://dx.doi.org/10.25298/2221-8785-2018-16-3-362-365.

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Maharaj, D., C. M. C. Fernandes, and A. P. Pinto. "Laryngopyocele (A report of two cases)." Journal of Laryngology & Otology 101, no. 8 (1987): 838–42. http://dx.doi.org/10.1017/s002221510010283x.

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Abstract:

A laryngocele is an air-filled dilatation of the saccule of the larynx. An in fected laryngocele is called a laryngopyocele. Our experience with two cases of laryngopyoceles are presented. Only 29 cases of laryngopyoceles have so far been reported in the literature (Illum and Nehen, 1980).Case one had a right-sided combined laryngopyocele and case two had a right-sided combined laryngopyocele and a left-sided combined laryngocele.Both our cases had their lesions excised via an external approach, as described by Yarington and Frazer (1966), with case two having a bilateral excision.

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Chijiwa, Keiichi, Ryu Kusaba, Kazunori Mori, and Tadashi Nakashima. "Surgical Resection of Mixed Laryngocele." Nihon Kikan Shokudoka Gakkai Kaiho 50, no. 3 (1999): 420–24. http://dx.doi.org/10.2468/jbes.50.420.

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Endo, Yoshihiko. "A Case of Combined Laryngocele." Practica Oto-Rhino-Laryngologica 103, no. 6 (2010): 563–67. http://dx.doi.org/10.5631/jibirin.103.563.

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Poduval, JayitaDas, and J. Jishana. "External laryngocele: Points to remember." Journal of Laryngology and Voice 3, no. 2 (2013): 67. http://dx.doi.org/10.4103/2230-9748.132061.

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Pradhan, Bibhu, R. CM Amatya, C. L. Bhusal, D. Singh, and B. Sharma. "LARYNGOCELE - REPORT OF A CASE." Journal of Nepal Medical Association 41, no. 144 (2003): 499–501. http://dx.doi.org/10.31729/jnma.707.

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Morshed, Kamal, Wiesław Gołąbek, Elżbieta Czekajska-Chehab, Anna Szymańska, and Marcin Szymański. "Imaging and management of laryngocele." Annales UMCS, Pharmacia 21, no. 2 (2008): 111–14. http://dx.doi.org/10.2478/v10080-008-0096-8.

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Vyskotová, Jana, Evald Záthurecký, Petra Gaul Aláčová, Petr Konečný, and Eva Mrázková. "Laryngocele and possibilities of treatment." Rehabilitace a fyzikální lékařství 29, no. 4 (2022): 164–68. http://dx.doi.org/10.48095/ccrhfl2022164.

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