Papalia Giuseppe Francesco, Ariyaratne Sisith, Vaiyapuri Sumathi, Botchu Rajesh, Kurisunkal Vineet
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.
Int Cancer Conf J. 2024 May 7;13(3):313-318. doi: 10.1007/s13691-024-00684-4. eCollection 2024 Jul.
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.
软骨肉瘤(CS)是第二常见的原发性恶性骨肿瘤,其特征是产生非骨样软骨基质。高达30%以上的CS患者会出现远处转移,肺部是最常见的转移部位。因此,CS软组织转移和浅表皮肤病变极为罕见。我们报告了一例女性患者,她出现了罕见的多发性软组织CS转移。该患者因左股骨近端病理性骨折行髓内钉内固定,随后因1-2级软骨肉瘤行全股骨近端假体置换,约4年后因股骨颈复发性3级软骨肉瘤累及骨盆而接受左半侧骨盆截肢术。在接下来的几年里,她因多处2级肺转移性软骨肉瘤接受了转移灶切除术。截肢14年多后,她出现了多个异常的浅表皮肤病变,全身磁共振成像显示有多个软组织转移病灶。切除的多个软组织病变的组织学检查证实为转移性软骨肉瘤。然后,她接受了进一步多灶性软组织转移性高级别软骨肉瘤的边缘切除术。与文献报道的其他病例中这些转移灶出现后生存率低不同,我们的患者在首次切除多发性软组织转移性软骨肉瘤后2年仍然存活,在诊断软骨肉瘤后约20年。软组织CS转移是一种罕见的情况,文献中描述的病例很少。本研究旨在让读者了解这种鲜为人知的CS表现形式。