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Enneking type III resection of pubic chondrosarcoma: A case report
A Zaizi1, R Badaoui1, A Rabah1
1Department of Orthopaedic Surgery & Traumatology II, Mohamed V Military Hospital, Faculty of Medicine and Pharmacy, Mohamed V University, Rabat, 10100, Morocco.
Annals of Medicine and Surgery (2012)
|February 11, 2022
Summary
This study presents a rare case of chondrosarcoma, a malignant cartilaginous tumor, in a 56-year-old male. Surgical resection was successful, with no recurrence after three years, highlighting effective treatment for this bone cancer.
Area of Science:
- Oncology
- Orthopedic Surgery
- Radiology
Background:
- Chondrosarcomas are rare malignant cartilaginous tumors typically affecting adults and the elderly.
- Common locations include pelvic and long bones, with diverse clinical presentations.
- Radiographic features often include bone expansion and heterogeneous calcifications.
Observation:
- A 56-year-old male presented with a fixed mass adhering to the right pubic bone.
- MRI revealed a lytic lesion in the right superior pubic rami.
- Surgical biopsy confirmed chondrosarcoma.
Findings:
- An en bloc resection of the chondrosarcoma was performed using a Pfannenstiel approach.
- The patient experienced no recurrence of the tumor three years post-surgery.
Implications:
- This case highlights the successful surgical management of pelvic chondrosarcoma.
- Early diagnosis and complete resection are crucial for favorable outcomes in chondrosarcoma patients.
- Further research into rare subtypes and treatment modalities for chondrosarcoma is warranted.
