What is Laryngocele?
A laryngocele is a rare congenital or acquired abnormal dilation (cystic expansion) of the saccule of the laryngeal ventricle, forming an air-filled or fluid-filled sac that communicates with the lumen of the larynx. The condition is classified by the ICD-10 code Q31.3 when congenital. Laryngoceles primarily affect the respiratory system, specifically the larynx (voice box). They are categorized into three types: internal laryngoceles, which remain within the laryngeal framework and may cause hoarseness and airway obstruction; external laryngoceles, which extend through the thyrohyoid membrane and present as a compressible neck mass; and combined (mixed) laryngoceles, which have both internal and external components. Key symptoms include hoarseness or voice changes, a sensation of a lump in the throat, dyspnea (difficulty breathing), stridor (noisy breathing), chronic cough, and a palpable neck mass that may enlarge with coughing or straining (Valsalva maneuver). If the laryngocele becomes filled with mucus rather than air, it is termed a laryngomucocele, and if it becomes infected, it is called a laryngopyocele, which can present with fever, pain, and rapid airway compromise requiring urgent intervention. Laryngoceles are more commonly observed in males and in adults, particularly those with occupations or activities that involve sustained increased intralaryngeal pressure, such as glass blowers and wind instrument players. Congenital forms are rare and may present in infancy or childhood. Diagnosis is typically made through imaging studies such as CT scan or MRI of the neck, along with laryngoscopy. Treatment depends on the size and symptoms. Small, asymptomatic laryngoceles may be monitored conservatively. Symptomatic or large laryngoceles are generally managed surgically, with options including endoscopic marsupialization (using CO2 laser) for internal types or an external surgical approach via lateral cervical incision for external or combined types. Prognosis after surgical treatment is generally excellent.
- Inheritance
- Sporadic
- Usually appears on its own, not inherited from a parent
- Age of Onset
- Variable
- Can begin at different ages, from infancy through adulthood
Treatments
Source: openFDA + DailyMed · NDA / BLA labels with structured indications · refreshed weekly
No FDA-approved treatments are currently listed for Laryngocele.
View clinical trials →Clinical Trials
View all trials with filters →Source: ClinicalTrials.gov · synced daily · phases, status, and PI names normalized at ingest
No actively recruiting trials found for Laryngocele at this time.
New trials open frequently. Follow this disease to get notified.
Specialists
View all specialists →Source: NPI Registry + PubMed · trial PI roles cross-referenced with ClinicalTrials.gov · ranked by match score (publications + PI activity + community signal)
No specialists are currently listed for Laryngocele.
Treatment Centers
8 centersSource: NORD Rare Disease Centers + NIH Undiagnosed Diseases Network (UDN) · centers verified active within last 12 months
Children's Hospital Colorado Rare Disease Program ↗
Children's Hospital Colorado
📍 Aurora, CO
👤 Boston Children's Hospital Rare Disease Program
🔬 UDNHarvard/MGH UDN Clinical Site ↗
Massachusetts General Hospital
📍 Boston, MA
🏥 NORDBoston Children's Hospital Rare Disease Program ↗
Boston Children's Hospital
📍 Boston, MA
👤 Boston Children's Hospital Rare Disease Program
🏥 NORDUCLA Rare Disease Day Program ↗
UCLA Health
📍 Los Angeles, CA
🏨 Children'sAnn & Robert H. Lurie Children's Hospital Genetics ↗
Lurie Children's Hospital
📍 Chicago, IL
👤 Boston Children's Hospital Rare Disease Program
🏥 NORDCincinnati Children's Hospital Medical Center ↗
Cincinnati Children's
📍 Cincinnati, OH
👤 Boston Children's Hospital Rare Disease Program
🏨 Children'sNationwide Children's Hospital Rare Disease Center ↗
Nationwide Children's Hospital
📍 Columbus, OH
👤 Boston Children's Hospital Rare Disease Program
🔬 UDNNIH Clinical Center Undiagnosed Diseases Program ↗
National Institutes of Health
📍 Bethesda, MD
Travel Grants
No travel grants are currently matched to Laryngocele.
Community
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Start the conversation →Latest news about Laryngocele
Source: PubMed + NIH RePORTER + openFDA + clinical-journal RSS · last 30 days · disease-tagged at ingest by AI extraction with human QC
No recent news articles for Laryngocele.
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Caregiver Resources
NORD Caregiver Resources
Support, advocacy, and financial assistance for caregivers of rare disease patients.
Mental Health Support
Rare disease caregiving can be isolating. Connect with counseling and peer support.
Family & Caregiver Grants
Financial assistance programs specifically for caregivers of rare disease patients.
Social Security Disability
Learn how rare disease patients may qualify for SSDI/SSI benefits.
Common questions about Laryngocele
What is Laryngocele?
A laryngocele is a rare congenital or acquired abnormal dilation (cystic expansion) of the saccule of the laryngeal ventricle, forming an air-filled or fluid-filled sac that communicates with the lumen of the larynx. The condition is classified by the ICD-10 code Q31.3 when congenital. Laryngoceles primarily affect the respiratory system, specifically the larynx (voice box). They are categorized into three types: internal laryngoceles, which remain within the laryngeal framework and may cause hoarseness and airway obstruction; external laryngoceles, which extend through the thyrohyoid membrane
How is Laryngocele inherited?
Laryngocele follows a sporadic inheritance pattern. Genetic counseling can help families understand recurrence risk and testing options.
Frequently asked questions about Laryngocele
Auto-generated from canonical disease facts (Orphanet, OMIM, ClinicalTrials.gov, openFDA, NPPES). Not a substitute for clinical guidance.
What is Laryngocele?
Laryngocele is a rare disease catalogued in international rare-disease ontologies (Orphanet ORPHA:2372). It is typically inherited as sporadic. Age of onset is generally variable. For verified primary sources, see the UniteRare Laryngocele page.
How is Laryngocele inherited?
Laryngocele follows sporadic inheritance. Genetic counseling is recommended for affected families to understand recurrence risk in offspring and the likelihood of unaffected siblings being carriers. Variants in the underlying gene(s) may be identified via clinical genetic testing.
Are there FDA-approved treatments for Laryngocele?
Approved treatments for Laryngocele are tracked from openFDA and DailyMed primary sources. Many rare diseases have no specific FDA-approved therapy; for those, supportive care and management of complications form the basis of clinical care. Orphan-drug-designation status is noted where applicable.
Are there clinical trials for Laryngocele?
Active clinical trials for Laryngocele are tracked daily from ClinicalTrials.gov. Trial availability changes frequently; check the UniteRare trial listings for the current count and recruitment status. Sponsors of rare-disease research often welcome inquiries even when a trial is not actively recruiting at a given moment.
How do I find a specialist for Laryngocele?
Verified Laryngocele specialists are identified through ClinicalTrials.gov principal-investigator records, peer-reviewed publication authorship (via PubMed), and the NPPES NPI registry. NORD-designated Centers of Excellence and NIH-affiliated rare-disease clinics are also tracked. UniteRare's specialist directory is updated continuously as new evidence becomes available.
See full Laryngocele page for complete clinical details, sources, and verified-specialist listings.
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