Evidence map›Paper›PMID 40242825›Full record

ArticleJournal of spine surgery (Hong Kong)2025

A 3D navigation-guided surgical resection of a rare case of sacral spine mesenchymal chondrosarcoma: a case report.

Abdulaziz Saber, Mohammed Khashab, Abdulhadi Turkistani, Moyassar Karami, Saleh Almaymoni, Mohamed Elkhalifa, Abdulhadi Algahtani, Abdullah Alhazmi

Abstract readCase Reports
In one paragraph

Article in Journal of spine surgery (Hong Kong), 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Abdulaziz SaberDepartment of Surgery, Orthopaedic Division, Ministry of National Guard-Health Affairs, Jeddah, Saudi Arabia.
Mohammed KhashabDepartment of Surgery, Orthopaedic Division, Ministry of National Guard-Health Affairs, Jeddah, Saudi Arabia.
Abdulhadi TurkistaniDepartment of Surgery, Orthopaedic Division, Ministry of National Guard-Health Affairs, Jeddah, Saudi Arabia.
Moyassar KaramiDepartment of Surgery, Orthopaedic Division, Ministry of National Guard-Health Affairs, Jeddah, Saudi Arabia.
Saleh AlmaymoniDepartment of Surgery, Orthopaedic Division, Ministry of National Guard-Health Affairs, Jeddah, Saudi Arabia.
Mohamed ElkhalifaDepartment of Surgery, Orthopaedic Division, Ministry of National Guard-Health Affairs, Jeddah, Saudi Arabia.
Abdulhadi AlgahtaniKing Abdullah International Medical Research Center, Jeddah, Saudi Arabia.
Abdullah AlhazmiDepartment of Surgery, Orthopaedic Division, Ministry of National Guard-Health Affairs, Jeddah, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Chondrosarcomas are a group of heterogeneous malignant cartilaginous neoplasms that arise from preexisting benign precursors. They can be divided into conventional (primary) chondrosarcomas, which account for 90% of cases, and nonconventional chondrosarcomas, which account for the remaining 10%. Mesenchymal chondrosarcoma (MCS) is a rare high-grade soft tissue tumor variant of nonconventional chondrosarcoma that is histologically characterized by a biphasic pattern of atypical cartilage with small round cells. Case Description: A 23-year-old female known case of ovarian cyst presented with a two-year history of low back pain and constitutional symptoms. Pelvic magnetic resonance imaging (MRI) with contrast showed a well-defined lesion with intermediate to high signals located at the right wing of the upper sacrum, at the level of S1-S2. The patient underwent a combined ultrasound and computed tomography-guided biopsy under local anesthesia and the immunochemical profile was positive for CD99 and S100 biomarkers. The patient underwent a two-stage procedure for a wide marginal tumor resection. Stage 1 was performed with an anterior approach; identification of the tumor margins was done followed by designing the cuts of the sacrum to achieve wide margins around the tumor. Stage 2 was performed with a posterior approach exposing L3 vertebrae down to the sacrum. Utilizing O-Arm Navigation for posterior margin allocation in addition to instrumentation. After 12 months post-operation, follow up revealed no evidence of recurrence. Conclusions: Limitation in accessibility to the axial skeleton and the neurovascular component, poses a challenge to treatment. Therefore, using neuro-navigation system and optimal adjuvant therapy should be studied further to improve the prognosis.

Indexed as

3D neuro-navigationcase reportMesenchymal chondrosarcoma (MCS)spinesurgical resection

Identifiers

PMID40242825
PMCPMC11998042

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.