Unusual soft tissue metastases in a patient with chondrosarcoma: a case report.

Chondrosarcoma Magnetic resonance imaging Malignancy Metastasis Soft tissue

Journal

International cancer conference journal
ISSN: 2192-3183
Titre abrégé: Int Cancer Conf J
Pays: Singapore
ID NLM: 101734231

Informations de publication

Date de publication:
Jul 2024
Historique:
received: 23 03 2024
accepted: 23 04 2024
pmc-release: 07 05 2025
medline: 4 7 2024
pubmed: 4 7 2024
entrez: 4 7 2024
Statut: epublish

Résumé

Chondrosarcoma (CS) is the second most frequent primary malignant bone tumour, characterized by production of non-osteoid cartilage matrix. Up to more than 30% of patients with CS present distant metastases, and the lungs represent the preferred site. Hence, CS soft tissue metastases and superficial cutaneous lesions are extremely rare. We report the case of a female who developed unusual multiple soft tissue CS metastases. This patient underwent left hindquarter amputation for recurrent grade 3 chondrosarcoma of the femoral neck with extension to the pelvis approximately 4 years after internal fixation with an intramedullary nail for pathological fracture of left proximal femur and subsequent total proximal femoral endoprosthetic replacement for grade 1-2 chondrosarcoma. In the following years, she underwent metastasectomy for several grade 2 pulmonary metastatic chondrosarcomas. More than 14 years after the amputation, she presented with multiple unusual superficial cutaneous lesions, and a whole-body magnetic resonance imaging demonstrated multiple soft tissue foci of metastatic disease. The histology of multiple soft tissue lesions excised confirmed metastatic chondrosarcoma. Then, she underwent marginal excision of further multifocal soft tissue metastatic high-grade chondrosarcoma. Unlike the poor survival from the onset of these metastases in the other cases reported in the literature, our patient is still alive 2 years after the first multiple soft tissue excision of metastatic chondrosarcoma, and approximately 20 years after the diagnosis of chondrosarcoma. Soft tissue CS metastases are a rare entity with few cases described in literature. This study aims to make the reader aware of this lesser-known CS manifestation.

Identifiants

pubmed: 38962050
doi: 10.1007/s13691-024-00684-4
pii: 684
pmc: PMC11217250
doi:

Types de publication

Journal Article

Langues

eng

Pagination

313-318

Informations de copyright

© The Author(s) under exclusive licence to The Japan Society of Clinical Oncology 2024. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

Déclaration de conflit d'intérêts

Conflict of interestThe authors declare that they have no conflict of interest.

Auteurs

Giuseppe Francesco Papalia (GF)

Department of Orthopedic Oncology, Royal Orthopedic Hospital, Birmingham, UK.
Research Unit of Orthopaedic and Trauma Surgery, Fondazione Policlinico Universitario Campus Bio-Medico, Via Alvaro del Portillo, 00128 Rome, Italy.

Sisith Ariyaratne (S)

Department of Musculoskeletal Radiology, Royal Orthopedic Hospital, Birmingham, UK.

Sumathi Vaiyapuri (S)

Department of Pathology, Royal Orthopedic Hospital, Birmingham, UK.

Rajesh Botchu (R)

Department of Musculoskeletal Radiology, Royal Orthopedic Hospital, Birmingham, UK.

Vineet Kurisunkal (V)

Department of Orthopedic Oncology, Royal Orthopedic Hospital, Birmingham, UK.

Classifications MeSH