Sinus pericranii
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Synopsis

SP typically presents at birth or in childhood as a mass on the midline frontal scalp that is nonpulsatile and that may increase in size with Valsalva maneuvers, Trendelenburg positioning, and crying. Most patients are asymptomatic, but nausea, vertigo, and headache may be associated. The headache may have sudden onset and typically waxes and wanes.
SP may be an isolated phenomenon, or it may occur in concert with other developmental abnormalities, including craniosynostosis or dural sinus hypoplasia, or syndromes, such as Noonan syndrome and Coffin-Siris syndrome.
Rare complications of SP include hemorrhage, infection, and retrograde sinus thrombosis.
Codes
ICD10CM:Q01.9 – Encephalocele, unspecified
SNOMEDCT:
50751005 – Sinus pericranii
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Diagnostic Pearls
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Differential Diagnosis & Pitfalls
- Deep infantile hemangioma
- Scalp arteriovenous malformation
- Meningocele
- Leptomeningeal cyst
- Atretic cephalocele
- Abscess
- Cephalohematoma
- Morphea (en coup de sabre)
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Last Reviewed:05/18/2022
Last Updated:05/19/2022
Last Updated:05/19/2022