Evidence map›Paper›PMID 41409854›Full record

ArticleSurgical neurology international2025

Multiple myeloma presenting as a giant osteolytic skull mass: Surgical challenges and pitfalls - A case report.

Shahd H I Abbastanira, Modar Mouhsen Monther, Muhammad Mukhtar Khan, Esraa Mohamed Abdullah Elameen

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In one paragraph

Article in Surgical neurology international, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Shahd H I AbbastaniraDepartment of Emergency Medicine, Dubai health, Dubai, United Arab Emirates.
Modar Mouhsen MontherDepartments of Neurosurgery, Rashid Hospital, Dubai health, Dubai, United Arab Emirates.
Muhammad Mukhtar KhanDepartments of Neurosurgery, Rashid Hospital, Dubai health, Dubai, United Arab Emirates.
Esraa Mohamed Abdullah ElameenDepartment of Internal Medicine, Zayed Military Hospital, Department of Health, Abu Dhabi, United Arab Emirates.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Osteolytic skull lesions can result from a broad spectrum of benign and malignant conditions, with multiple myeloma (MM) being a significant malignant cause in adults. Although skull involvement is relatively common in MM, giant exophytic lesions with extensive calvarial destruction and intracranial extension are exceedingly rare and pose diagnostic and therapeutic challenges. Case Description: A 48-year-old male presented with progressive right-sided weakness and a visibly enlarging skull mass. Computed tomography (CT) brain scan revealed a large, well-defined, enhancing mass measuring 9.02 × 7.29 × 6.5 cm, located extra-axially, causing significant compression of the left cerebral hemisphere and ventricle. Magnetic resonance imaging confirmed a large, destructive left frontoparietal lesion with marked bone erosion, and mass effect on the underlying cerebrum. The patient underwent preoperative embolization, followed by surgical resection of the tumor with wide margins and decompression, including removal of the involved skull. Histopathological and immunohistochemical analyses confirmed a high-grade malignant plasma cell neoplasm consistent with MM. Subsequent positron emission tomography-CT and bone marrow biopsy demonstrated systemic disease. The hematology team took over care of the patient for definitive systemic therapy. Conclusion: Giant exophytic skull lesions due to MM are rare and often mimic other neoplastic conditions. This case underscores the importance of early recognition, thorough diagnostic workup, and a multidisciplinary treatment approach. Radical neurosurgical resection combined with systemic oncological therapy is essential to optimize patient outcomes in such uncommon but aggressive presentations.

Indexed as

Case reportMultiple myelomaNeurosurgeryOsteolytic bone diseasePlasma cell neoplasmSkull lesion

Identifiers

PMID41409854
PMCPMC12707699

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