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Updated: Dec 5, 2025

Image Acquisition using Portable Sonography for Emergency Airway Management
Published on: September 28, 2022
Airway obstruction as the primary manifestation of infantile thyroid hemangioma
Yujian Liang1, Ronghui Pu1, Xueqiong Huang1
1Department of Pediatric, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, P. R. China.
Insights
This study reports the first case of infant capillary thyroid hemangioma, a rare condition presenting with airway obstruction. Combined surgical and propranolol treatment led to significant symptom improvement.
Area of Science:
- Pediatric Endocrinology
- Vascular Anomalies
- Thyroid Pathology
Background:
- Thyroid hemangiomas are rare, predominantly affecting adults, with only a few pediatric cases documented.
- Capillary hemangiomas of the thyroid are exceptionally rare, and no infant cases have been previously reported.
- This case highlights a unique presentation of a primary capillary hemangioma in an infant.
Observation:
- A 2-month-old infant presented with severe airway obstruction (laryngeal wheezing, dyspnea) due to thyroid hemangioma.
- Imaging revealed bilateral thyroid lesions, but definitive diagnosis required postoperative histopathology.
- The infant had normal thyroid function despite the presence of the thyroid mass.
Findings:
- Histopathological examination confirmed a diagnosis of capillary thyroid hemangioma.
- The infant's airway obstruction symptoms significantly improved following a combined treatment approach.
- Treatment involved surgical intervention and oral propranolol administration.
Implications:
- This case expands the known spectrum of thyroid hemangioma presentations in infants.
- Early consideration of thyroid hemangioma is crucial when imaging reveals well-defined, capsulated thyroid masses.
- A multimodal treatment strategy, including propranolol, can be effective for infant thyroid hemangioma.
Background:
Thyroid hemangioma mostly occurs in adults and is extremely rare in infants. So far, only four pediatric cases of thyroid hemangioma have been reported, one of which has only been clinically diagnosed. Most of the reported cases are of cavernous hemangiomas; capillary hemangioma cases are very rare. To date, there are no reports on capillary thyroid hemangioma in an infant. Therefore, here we present the case of an infant with a primary capillary hemangioma of the thyroid gland, and discuss its treatment and follow-up.
Case Presentation:
A2-month-old infant with normal thyroid function presented with airway obstruction as the primary manifestation of thyroid hemangioma. The main symptoms were laryngeal wheezing and dyspnea. Ultrasonography revealed hypoechoic lesions at the lower pole of the bilateral thyroid. Computed tomography revealed enlargement of the thyroid gland, inhomogeneous parenchyma enhancement, and multiple thyroid nodules. However, these imaging modalities were unable to provide an exact diagnosis and the nature of the mass remained unknown prior to an operation. Therefore, a postoperative histopathological examination was undertaken, which revealed capillary thyroid hemangioma. The symptoms significantly improved by a combined treatment involving surgery and oral propranolol.
Conclusion:
When a well-defined capsulate mass is detected on the medical image, the possibility of primary thyroid hemangioma must be considered.
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