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Published on: June 15, 2020
Postcricoid vascular abnormalities: hemangiomas, venous malformations, or anatomic variant
Thorsen W Haugen1, W Edward Wood, Cecilia Helwig
1Pediatric Otolaryngology Head and Neck Surgery, Geisinger Medical Center, Danville, PA 17822, USA. thorsen.haugen@gmail.com
Insights
Pressure-dependent postcricoid masses (PDPCM) in children are likely an anatomic variant, not hemangiomas. Most cases can be safely observed without intervention, simplifying diagnosis and management.
Area of Science:
- Pediatric Otolaryngology
- Pediatric Airway Disorders
- Vascular Lesions
Background:
- Previously, pressure-dependent postcricoid masses (PDPCM) in children were often misdiagnosed as hemangiomas or vascular malformations.
- This series represents the largest to date investigating these specific pediatric airway lesions.
Purpose of the Study:
- To present ten pediatric cases of PDPCM, proposing they represent an anatomic variant.
- To review the presentation, diagnosis, and management of PDPCMs in the largest reported series.
Main Methods:
- Ten patients aged five weeks to nine months were diagnosed and managed through observation or intervention.
- Interventions included gastrostomy tube, fundoplication, Propranolol therapy, and tracheotomy for a patient with CHARGE association.
Main Results:
- No significant interval changes in size or appearance were observed in the PDPCMs.
- Eight out of ten patients experienced positive outcomes with observation alone.
Conclusions:
- The majority of PDPCMs are likely an anatomic variant, distinct from hemangiomas or vascular malformations.
- Awake flexible fiberoptic laryngoscopy is the primary diagnostic tool; direct laryngoscopy and bronchoscopy are recommended for symptomatic cases due to high incidence of synchronous airway pathology.
- Observation is the recommended management for most PDPCMs, as active treatment is often unnecessary.
Objective:
Ten children with pressure-dependent postcricoid masses (PDPCM) previously referred to in the literature as hemangiomas or vascular malformations are presented. We propose these lesions represent an anatomic variant. We review previously reported cases, and report the presentation, diagnosis, and management of the patients in our series, the largest series to date.
Methods:
Ten patients, aged five weeks to nine months, were diagnosed, and treated or observed. Of the patients undergoing intervention, one was treated with a gastrostomy tube, fundoplication, and Propranolol therapy; and the other with CHARGE association underwent a tracheotomy.
Results:
No PDPCMs demonstrated significant interval change in size or appearance, and eight of ten patients did well with observation.
Conclusion:
Based on current information, the majority of PDPCMs likely represent an anatomic variant rather than a hemangioma or vascular malformation. Diagnosis is most readily made with awake flexible fiberoptic laryngoscopy. Because the incidence of synchronous airway pathology is high, direct laryngoscopy and bronchoscopy without routine biopsy is recommended for symptomatic patients. Imaging should be individualized and may be helpful for ambiguous cases. Although numerous treatment modalities have been advocated based on the presumptive diagnosis of a hemangioma, treatment of PDPCMs is not necessary in the majority of cases, as most patients may be safely observed.
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