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Published on: October 11, 2022
[A giant thoracoabdominal tumor--hereditary multiple exostoses]
C Nistor1, A Ciuche, M Davidescu
1Clinica de Chirurgie Toracică, Spitalul Clinic de Urgenţă Militar Central Bucureşti, România.
Insights
Hereditary multiple exostoses (HME) can cause large tumors. This case details the successful surgical removal of a 2.6 kg osteochondroma from a teenager, restoring function and aesthetics.
Area of Science:
- Orthopedics
- Genetics
- Surgical Oncology
Background:
- Hereditary multiple exostoses (HME), or osteochondromatosis, is an autosomal dominant disorder characterized by skeletal osteochondromas.
- Patients often require multiple orthopedic interventions for limb deformities.
Observation:
- A 17-year-old male with a history of HME presented with a giant osteochondroma (2.6 kg) at the thoraco-abdominal border.
- The tumor involved the ribs, thoracic wall, abdominal wall, and retroperitoneal space.
Findings:
- The patient underwent successful total tumor resection, including thoracic and abdominal parietectomy.
- Reconstruction involved a dual-mesh soft tissue patch and diaphragm reinsertion, preserving function and aesthetics.
Implications:
- This case highlights the feasibility of radical surgical management for massive HME-associated tumors.
- Successful surgical outcomes can be achieved with meticulous surgical planning and reconstruction, improving patient quality of life.
Abstract:
Hereditary multiple exostoses (HME), also known as osteochondromatosis, is an inherited, autosomal dominant disorder in which multiple osteochondromas develop throughout the skeleton. We present the case of a 17 years old boy diagnosticated with HME with multiple prior orthopedic interventions for upper and lower limbs deformant osteochondromas. He was admitted in our service for a giant osteochondroma localized at the left thoraco-abdominal border arising from C11, C12 ribs, involving the thoracic postero-bazal wall, the abdominal posterior wall and practically the entire left retroperitoneal space. We performed the total resection of this giant tumor (2.6 kg) with postero-inferior thoracic parietectomy (10 to 12 ribs) and abdominal postero-lateral parietectomy followed by the thoraco-abdominal parietal reconstruction with a dual-mesh soft tissue patch, after the high reinsertion of the left diaphragm. The postoperative results were very good from both points of view: esthetical and functional, with preservation of the diaphragm activity and the anatomical reposition of the abdominal viscera. The paper refers to the etiopathogenesis, clinical symptoms, diagnostic, and therapeutic considerations of HME.
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