ArticleThe American journal of case reports2022
A Rare Case of an Intracranial Dermoid Cyst with Atypical Appearance on Computed Tomography and Magnetic Resonance Imaging.
Article in The American journal of case reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Who cites it
6 citing papers in PubMed, 6 citations in OpenAlex.
- Ruptured intracranial dermoid cyst as an incidental finding: Case report.Radiology case reports · 2026Article
- Progressive hemorrhagic intracranial dermoid cyst: A case report with imaging and diagnostic considerations.Radiology case reports · 2025Article
- An infected intradural dermoid cyst associated with a complete dermal sinus of the posterior cranial fossa: A case report and literature review.SAGE open medical case reports · 2024Article
- Fat droplets in the cerebrospinal fluid (CSF) spaces of the brain.AIMS neuroscience · 2024Article
- An Atypical Case of Intracranial Dermoid Cyst in an Adult Female: A Case Report and Literature Review.Cureus · 2023Article
- Dermoid Cyst in the Posterior Fossa Associated With Dermal Sinus and Abscess Formation: A Case Report.Cureus · 2023Article
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Authors and funding
3 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
BACKGROUND Dermoid cysts are rare benign intracranial tumors that usually present classic computed tomography (CT) and magnetic resonance imaging (MRI) characteristics, allowing for relatively simple diagnostic confirmation. Atypical imaging features can occur due to their diverse ectodermal-derived content, which can result in a diagnostic dilemma. Making an accurate diagnosis is essential for adequate management. CASE REPORT We present a case of a 39-year-old woman with past medical history of increased blood pressure, presenting with worsening headaches non-refractory to medication. Imaging revealed an extra-axial lesion within the midline posterior fossa with an occipital transdiploic linear channel. The lesion was T2 profoundly hypointense on brain MRI, and prominently hyperdense on non-contrast CT scan. Catheter angiography excluded vascular etiology. After complete lesion resection, results of the histopathologic examination were consistent with a dermoid cyst. Dermoid cysts that are hyperdense on CT and hypointense on T2-WI are extremely rare. CONCLUSIONS Complete surgical resection is the treatment of choice for most dermoid cysts. Atypical radiologic features, in an already rare intracranial tumor, can delay correct diagnosis and management. Recognition of these findings is therefore important for adequate imaging analysis of these lesions.
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