Pitfalls of Distinguishing Skull Metastases from Paragangliomas: A Case Report of a “Pseudo-angioma” Bone Metastasis
A 22-year-old woman with persistent headaches was diagnosed with a right parietal bone lytic lesion with a sunburst pattern, suspected to be either an intraosseous hemangioma or a Langerhans cell histiocytosis. Five years later, progressively increased skull bone destruction, identification of retroperitoneal and lumbar vertebra lesions, and a biopsy of the skull led to the diagnosis of a retroperitoneal paraganglioma with bone metastases. Genetic testing identified an <i>SDHB</i>mutation. This case underscores the diagnostic challenge of metastases of paraganglioma mimicking hemangiomas and thus delaying appropriate management. · - Skull metastases from paragangliomas can present with a pseudoangiomatous appearance that mimics a hemangioma.. · - The presence of an SDHB mutation is associated with more aggressive forms of paraganglioma with higher rates of metastasis and disease-specific morbidity.. · - Lifelong monitoring for paraganglioma is essential due to the risk of late metastasis, especially bone metastasis..
Authors
- Valérie Bousson (ORCID: https://orcid.org/0000-0002-0544-3228)
- Annouk Bisdorff
- Victoire Roblot (ORCID: https://orcid.org/0000-0002-7227-4751)
- Anne Laure Bernat (ORCID: https://orcid.org/0000-0002-3659-6518)
- Elisa Deflorenne
- Annelise Dunas
Institutions
- Université Paris Cité (FR)
- Assistance Publique – Hôpitaux de Paris (FR)
- Hôpital Européen Georges-Pompidou (FR)
- Hôpital Fernand-Widal (FR)
- Hôpital Lariboisière (FR)
Publication Details
- Journal
- Seminars in Musculoskeletal Radiology
- Published
- 2025-07-16
- DOI
- https://doi.org/10.1055/s-0045-1809073
- Primary Topic
- Adrenal and Paraganglionic Tumors
- Type
- article
- Field-Weighted Citation Impact
- 0.00