Imaging of the Hyrtl Fissure: A Rare Cause of Congenital CSF Otorrhea
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Updated: Jun 19, 2026

State of the Art Cranial Ultrasound Imaging in Neonates
Published on: February 2, 2015
Jamie E Clarke1, John Manov1, Josephine M Ndolo2
1From the Department of Radiology (J.E.C., J.M., G.S.), Jackson Memorial Hospital, Miami, Florida.
Abstract:
Hyrtl fissure is a rare cause of congenital CSF otorrhea in infants, with only a few cases previously described in the English literature. Given the predisposition to repeated ear and intracranial infections, identification of this bony anomaly is critical in the diagnosis and management of recurrent meningitis or otitis media in a child, especially in the presence of CSF otorrhea. We describe 3 cases of this entity with a specific focus on the embryologic basis of the etiology and conventional and advanced imaging features of this unique entity.
Insights
Hyrtl fissure, a rare congenital condition, can cause cerebrospinal fluid (CSF) leakage from the ear in infants. Early diagnosis is crucial to prevent recurrent ear and brain infections.
Area of Science:
- Otolaryngology
- Pediatric Neurology
- Medical Imaging
Background:
- Hyrtl fissure is a rare congenital anomaly.
- It can lead to cerebrospinal fluid (CSF) otorrhea in infants.
- This condition predisposes infants to recurrent ear and intracranial infections.
Purpose of the Study:
- To describe three cases of Hyrtl fissure.
- To focus on the embryologic basis of the condition.
- To highlight the conventional and advanced imaging features.
Main Methods:
- Case series presentation.
- Review of embryologic development.
- Analysis of imaging findings (conventional and advanced).
Main Results:
- Three cases of Hyrtl fissure with CSF otorrhea were identified.
- The embryologic origin of the anomaly was discussed.
- Characteristic imaging features were presented.
Conclusions:
- Hyrtl fissure is a critical diagnosis in infants with recurrent meningitis or otitis media.
- Identification is vital for appropriate management and prevention of infections.
- Imaging plays a key role in diagnosing this rare bony anomaly.
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