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Artykuły w czasopismach na temat „Internal laryngocele”

Autor: Grafiati

Data publikacji: 3 czerwca 2025

Data aktualizacji: 31 lipca 2025

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1

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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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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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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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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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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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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8

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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9

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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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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11

Bhat, Vinay S., Yanamadala Sobhan, and KS Ravi. "A Rare Case of Internal Laryngopyocele presenting with Stridor." International Journal of Phonosurgery & Laryngology 4, no. 1 (2014): 20–22. http://dx.doi.org/10.5005/jp-journals-10023-1073.

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ABSTRACT A laryngocele is an abnormal elongation and expansion of the saccule of the laryngeal ventricle. When the neck of the laryngocele is obstructed, it becomes filled with mucus of glandular secretion and is altered to a laryngomucocele. When this lesion becomes infected, laryngopyocele is formed. In view of the general rarity of laryngopyoceles and even more so, one causing acute airway obstruction, it was decided to report an instance of the latter type. The clinical features and management of this rare case has been described. How to cite this article Bhat VS, Sobhan Y, Ravi KS. A Rare

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12

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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Kim, Christine M., Michael A. Holliday, and Kenneth A. Newkirk. "Laryngeal Pilar Cyst Masquerading as an Internal/External Laryngocele." Clinical Medicine Insights: Ear, Nose and Throat 11 (January 2018): 117955061881591. http://dx.doi.org/10.1177/1179550618815917.

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Objectives: This study aimed to document and describe a case of a laryngeal pilar cyst and to review the literature. Methods: We describe the case of a 65-year-old woman with a laryngeal pilar cyst presenting with occasional ear pain and positional dyspnea, with imaging studies suggesting external/internal laryngocele. We also review the existing clinical literature. Results: Pilar cysts are adnexal skin lesions most commonly found in the scalp of elderly women. They generally have a benign course, but in rare instances single or multiple foci of proliferating cells can lead to the neoplastic

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Saindani, Shradha, Sachin Gandhi, and Renuka Mundalik. "Congenital internal laryngocele: Our experience of six patients." Journal of Laryngology and Voice 13, no. 1 (2023): 1. http://dx.doi.org/10.4103/jlv.jlv_13_23.

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Szwarc, Brian J., and Haskins K. Kashima. "Endoscopic Management of a Combined Laryngocele." Annals of Otology, Rhinology & Laryngology 106, no. 7 (1997): 556–59. http://dx.doi.org/10.1177/000348949710600704.

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A 70-year-old woman presented with hoarseness, foul sputum, and a soft neck mass. Clinical and radiographic examination disclosed findings consistent with a combined internal and external laryngopyocele. Antibiotics, throat irrigations, and warm packs applied to the neck resulted in full resolution of the neck mass and subtotal regression of the supraglottic swelling. Endoscopic vestibulectomy was performed with a carbon dioxide laser; neither residual neck mass nor a tract leading to the extralaryngeal neck swelling was detected. The immediate and long-term clinical course has been uneventful

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Mensiz, Ercan, Mustafa Tüz, Orhan Oyar, Harun Doğru, and Hasan Yasan. "A case of orbital emphysema associated with internal laryngocele." Auris Nasus Larynx 30, no. 2 (2003): 197–200. http://dx.doi.org/10.1016/s0385-8146(03)00046-4.

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Collins, William O., and George H. Zalzal. "Internal Jugular Vein Phlebectasia Masquerading as an External Laryngocele." Archives of Otolaryngology–Head & Neck Surgery 131, no. 2 (2005): 163. http://dx.doi.org/10.1001/archotol.131.2.163.

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Hirvonen, Timo Petteri. "Endoscopic CO₂ Laser Surgery for Large Internal Laryngocele." ORL 63, no. 1 (2001): 58–60. http://dx.doi.org/10.1159/000055708.

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Zagkou, Eirini, Thomas Aldridge, Peyman Alam, and Peter A. Brennan. "Spontaneous rupture of an internal laryngocele after neck dissection: a rare complication." British Journal of Oral and Maxillofacial Surgery 54, no. 10 (2016): 1128–30. http://dx.doi.org/10.1016/j.bjoms.2016.03.015.

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Andreou, Zenon, Premjit S. Randhawa, Paul O'Flynn, and Francis M. Vaz. "Endoscopic Management of an Internal Laryngopyocele Presenting with Acute Airway Obstruction." Case Reports in Surgery 2011 (2011): 1–3. http://dx.doi.org/10.1155/2011/873613.

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Statement of Problem. Laryngocele is a rare laryngeal disease, where there is an abnormal dilatation of the saccule of the laryngeal ventricle. It can either be internal or external, and a laryngopyocele is a rare complication of this anomaly. Internal laryngopyoceles can prove difficult to manage, as they often present with airway compromise.Method of Study. Case Report.Results. We present a case of a laryngopyocele that was successfully managed with suspension laryngoscopy and endoscopic marsupialisation and resection. To our knowledge, this is the first such case described in the literature

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Anand, Aishwarya, Anand Veluswamy, and Asheesh Dora Ghanpur. "Endoscopic management of internal laryngopyocele presenting with acute airway obstruction." Perspectives in Medical Research 11, no. 2 (2023): 71–73. http://dx.doi.org/10.47799/pimr.1102.14.

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Abstract Introduction: A laryngocele is an abnormal dilatation of the laryngeal saccule. It is asymptomatic most of the time so its true incidence is unknown. Depending on the site, symptoms may vary from a lump sensation in the throat to breathing difficulty. Radiologic confirmation of the diagnosis is a must. Report: A 50-year-old diabetic gentleman presenting with acute airway obstruction was evaluated and found to have an internal laryngopyocele which was managed with IV antibiotics and an endoscopic approach (draining and marsupialization) after securing the airway by tracheostomy. A revi

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Rao, Karthik N., Shrinivas S. Chavan, Vitthal D. Kale, Amol Hekare, Archana Sylendran, and Abishek Khond. "IJV Phlebectasia: an approach algorithm." International Surgery Journal 4, no. 10 (2017): 3570. http://dx.doi.org/10.18203/2349-2902.isj20174543.

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Internal jugular venous (IJV) Phlebectasia are rare disorders. It is generally diagnosed at an early age, usually unidentified or misdiagnosed or ignored because of the scarcity of the knowledge on the disorder. We encountered a case of 7-year-old child with a right sided intermittent neck swelling which mimicked as an external laryngocele. But, the diagnosis of IJV Phlebectasia was made on “dynamic” ultrasound (USG) doppler study. Cervical adenopathy, mediastinal masses, tuberculosis and certain syndromes of connective tissue disorders were ruled out. The child was managed conservatively with

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Raos, M., J. Marković, and S. Schmidt. "Value of Valsalva’s manoeuvre in diagnosis of neck mass in children." Paediatria Croatica 54, no. 2 (2010): 111–15. http://dx.doi.org/10.13112/pc.841.

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During Valsalva’s manoeuvre the following neck masses could be seen: laryngocele, external laryngeal diverticle, pharyngocele, jugular vein phlebectasia, apical lung herniation, superior mediastinal cyst or tumour. In the present paper three children with neck mass visible during Valsalva’s manoeuvre are presented. In a child with neck mass appearing on the right lateral neck, an internal jugular vein phlebectasis was found. In two children the neck mass appeared in jugulum, above the sternum. In one child, the clinical finding pointed to an apical lung herniation (crepitation in the neck mass

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Aidonis, Ioannis, Nikolaos Lazaridis, Maria Piagkou, Nikolaos Anastasopoulos, and Konstantinos Natsis. "A Large Laryngeal Mucocele Causing Progressive upper Airway Obstruction and Cervical Swelling." Acta Medica (Hradec Kralove, Czech Republic) 60, no. 4 (2017): 157–59. http://dx.doi.org/10.14712/18059694.2018.12.

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Laryngocele (LC) is an uncommon clinical entity, occasionally associated with fatal complications. If its neck becomes obstructed, mucous accumulates and then a laryngeal mucocele (LMC) is formed. Reports of LMCs are rare in the literature. A fluid-filled combined LMC in a 48 year-old Greek construction worker with presenting symptoms of cervical swelling and dysphonia is described. The male patient was surgically treated via an external approach. A LC rarely becomes symptomatic and infection unusually occurs. Magnetic resonance imaging depicts in detail the size, extension and structure of th

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Vedasalam, S., F. Sipaul, and G. Porter. "Internal laryngocoele and referred otalgia." Case Reports 2010, no. 24 1 (2010): bcr0420102912. http://dx.doi.org/10.1136/bcr.04.2010.2912.

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Sakci, Zakir, Yener Aydin, and Hayri Ogul. "Reformatted thoracic computed tomography imaging findings of an internal laryngocoele." British Journal of Hospital Medicine 82, no. 6 (2021): 1–2. http://dx.doi.org/10.12968/hmed.2021.0043.

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Stocker, Derek J., William F. Kelly, Thomas M. Fitzpatrick, Victor J. Bernet, and Henry B. Burch. "Bilateral External Laryngoceles Following Radioiodine Ablation for Graves Disease." Archives of Internal Medicine 162, no. 17 (2002): 2007. http://dx.doi.org/10.1001/archinte.162.17.2007.

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Wong, B. Y. W., D. R. Strachan, and E. L. Loney. "Duplication of internal jugular veins: case report." Journal of Laryngology & Otology 124, no. 3 (2009): 341–44. http://dx.doi.org/10.1017/s0022215109990855.

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AbstractObjectives:We report a rare case of internal jugular vein duplications, in order to raise the level of awareness of this anomaly amongst ENT surgeons, radiologists and intensive care practitioners. We briefly review and discuss the related literature.Case report:Duplicated internal jugular veins are a rare anatomical finding. They may be subclinical, or may present with neck swellings that may be mistaken for laryngocoeles or branchial cysts. We present a case of bilateral internal jugular vein duplication in a young adult. The referral was made on the basis of intermittent neck swelli

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Moor, James W., and M. Iqbal J. Khan. "Growth hormone abuse and bodybuilding as aetiological factors in the development of bilateral internal laryngocoeles. A case report." European Archives of Oto-Rhino-Laryngology 262, no. 7 (2005): 570–72. http://dx.doi.org/10.1007/s00405-004-0861-6.

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James, Danielle L., Stephen Garry, Mel Corbett, and John Lang. "Mixed infected laryngocoele presenting as airway obstruction: a case report." Journal of Surgical Case Reports 2021, no. 2 (2021). http://dx.doi.org/10.1093/jscr/rjaa615.

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Abstract Laryngocoele is a rare entity, defined as an abnormal cystic dilatation of saccule of the laryngeal ventricle. Three types of laryngocele have been described, based on their relation to the thyrohyoid membrane: internal, external or mixed type. Symptoms are variable, including neck swelling, shortness of breath, dysphonia and fever, if the laryngocoele becomes infected. Patients may also present in extremis with airway obstruction. We present the case of a healthy 34-year-old gentleman with acute airway obstruction due to a mixed infected laryngocoele. Flexible nasoendoscopy showed a

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Balasubramanian, Thiagarajan. "Laryngocele A Review." Otoloaryngology Online, June 19, 2017. https://doi.org/10.5281/zenodo.812884.

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Laryngocele is a rare condition characterized by benign dilatation of laryngeal saccule. It may be asymptomatic in a majority of patients, but could present with neck swelling, hoarseness, cough and stridor. Clinically three types of Laryngocele have been documented i.e. Internal, External and Combined. Old published literature suggests that this condition is common in glass blowers. This article attempts to re-view published literature in the scenario of author's experience with 3 cases. This record was migrated from the OpenDepot repository service in June, 2017 before shutting down.

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PS, Suhaima. "Bilateral combined laryngocoele: A case report." Journal of Clinical Images and Medical Case Reports 5, no. 3 (2024). http://dx.doi.org/10.52768/2766-7820/2916.

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Laryngocele, an uncommon condition, involves an abnormal cystic enlargement of the saccule within the larynx, often containing air and communicating with the laryngeal space. It can manifest as internal, external, or mixed types. Here, we present a case of laryngocele that posed a diagnostic challenge initially but was eventually confirmed through radiological examination. Subsequently, the patient underwent surgical intervention via combined approach. Our article underscores the necessity of employing a combined open and Endo laryngeal approach for the comprehensive removal of a mixed laryngo

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Booke, Hendrik, Carsten Dalchow, and Michael Booke. "Almost complete airway occlusion due to an internal laryngocele." Oxford Medical Case Reports 2021, no. 8 (2021). http://dx.doi.org/10.1093/omcr/omab067.

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de Campos, Marcos Álvares, Elisa Carvalho de Siqueira, Fabricio Tinôco Alvim de Souza, et al. "Mixed laryngocele mimicking thyroid nodule." Journal of Ultrasound, January 18, 2022. http://dx.doi.org/10.1007/s40477-021-00614-7.

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Johnny Mao, Michael A. Carron. "Internal Laryngocele and Zenker�s Diverticulum Masquerading as a Laryngeal Fracture and Esophageal Perforation and Rupture." Journal of Otology & Rhinology 01, no. 02 (2012). http://dx.doi.org/10.4172/2324-8785.1000104.

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