Evidence map›Paper›PMID 40851963›Full record

ArticleAnnals of medicine and surgery (2012)2025

Synchronous multifocal osteosarcoma with atypical adrenal metastasis: a case report and literature review.

Habeeb H Awwad, Anas K Assi, Zaina A Khaled, Haneen Owienah, Mohand Abulilhya, Khaled S Azzam, Bahaa Bashir, Thaer Sweileh, Feras Eleyan

Abstract readCase Reports
In one paragraph

Article in Annals of medicine and surgery (2012), 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

9 authors.

Habeeb H AwwadFaculty of Medicine, Al-Quds University, Jerusalem, Palestine.
Anas K AssiFaculty of Medicine, Al-Quds University, Jerusalem, Palestine.
Zaina A KhaledFaculty of Medicine, Al-Quds University, Jerusalem, Palestine.
Haneen OwienahRadiology Department, Istishari Arab Hospital, Ramallah, West Bank, Palestine.
Mohand AbulilhyaPathology department, Istishari Arab Hospital, Ramallah, West Bank, Palestine.
Khaled S AzzamRadiology Department, Istishari Arab Hospital, Ramallah, West Bank, Palestine.
Bahaa BashirOncology department, Istishari Arab Hospital, Ramallah, West Bank, Palestine.
Thaer SweilehRadiology Department, Istishari Arab Hospital, Ramallah, West Bank, Palestine.
Feras EleyanOncology department, Istishari Arab Hospital, Ramallah, West Bank, Palestine.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction and importance: The most prevalent malignant bone tumor that typically impacts young adults is osteosarcoma. Synchronous multifocal osteosarcoma (SMOS) with metastasis is extremely rare, defined by the occurrence of various bone lesions being presented at the time of diagnosis. This report describes a rare case of SMOS with adrenal involvement and a simultaneous abdominal aortic aneurysm (AAA). Case presentation: We report a case of a 34-year-old Palestinian male with a history of hypertension and gout who presented with lower back and right leg pain. Imaging studies showed multiple lytic lesions in the lumbar spine, pelvis, and femur, confirming the presence of a metastatic disease. A whole-body CT scan revealed an adrenal mass and an AAA. A core needle biopsy confirmed the diagnosis of high-grade SMOS with metastasis. Clinical discussion: Osteosarcoma is the primary cancerous bone tumor that frequently impacts teenagers and young adults. Although multifocal osteosarcoma is rare, it is characterized by its aggressive nature and its possibility to metastasize. SMOS, which is a less common type, makes up only 0.6% of cases. Metastatic SMOS commonly impacts bones, including the pelvis, spine, and femur. While it is typical for cancer to spread to places like the lungs, the rare occurrence of metastasis to organs like the adrenal glands makes diagnosis and treatment more challenging. Conclusion: This case highlights the challenges in diagnosing and managing SMOS with unusual metastatic patterns and significant comorbidities. It emphasizes the importance of using interdisciplinary, comprehensive methods to optimize patient outcomes in such clinical scenarios.

Indexed as

abdominal aortic aneurysm (AAA)adrenal metastasislytic lesionsosteosarcomasynchronous multifocal osteosarcoma (SMOS)

Identifiers

PMID40851963
PMCPMC12369787

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