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..

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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
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article

Pitfalls of Distinguishing Skull Metastases from Paragangliomas: A Case Report of a “Pseudo-angioma” Bone Metastasis

Valérie Bousson, Annouk Bisdorff, Victoire Roblot, Anne Laure Bernat et al.
1 links
Seminars in Musculoskeletal Radiology
Adrenal and Paraganglionic Tumors
article

Pitfalls of Distinguishing Skull Metastases from Paragangliomas: A Case Report of a “Pseudo-angioma” Bone Metastasis

Valérie Bousson, Annouk Bisdorff, Victoire Roblot, Anne Laure Bernat, Elisa Deflorenne, Annelise Dunas
article en

Abstract

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..

Seminars in Musculoskeletal RadiologyVol. 29(04)
Université Paris Cité (FR), Assistance Publique – Hôpitaux de Paris (FR), Hôpital Européen Georges-Pompidou (FR), Hôpital Fernand-Widal (FR), Hôpital Lariboisière (FR)
Good health and well-being
Openalex Percentile: Top 70%
Adrenal and Paraganglionic Tumors
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