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. 2014;5(12):968-71.
doi: 10.1016/j.ijscr.2014.10.008. Epub 2014 Oct 18.

Chest wall secondary chondrosarcoma arising from enchondroma in a young Asian female

Affiliations

Chest wall secondary chondrosarcoma arising from enchondroma in a young Asian female

Chih Chiang Nieh et al. Int J Surg Case Rep. 2014.

Abstract

Introduction: Enchondromas are benign tumours derived from cartilaginous tissue and they rarely undergo malignant transformation unless they occur in multiple sites such as in the case of Ollier disease.

Presentation of case: We report a rare case of a 36-year-old Chinese female, without any past medical history, who had a right chest wall tumour which was initially diagnosed to be benign, for which she was loss to follow up. The mass had been stable in size for the past 7 years until recently, when it gradually grew bigger. computed tomography (CT) scan of the thorax revealed that the mass had invaded the right chest wall suggestive of malignant change. She subsequently underwent an elective open right chest wall resection of the mass and chest wall reconstruction with mesh. A 3cm by 3cm tumour arising from the anterior aspect of the 4th rib was found intra-operatively. Post-operative course was uneventful. Histologically, the mass was confirmed to be chrondrosarcoma and resection margins were negative. The patient was discharged on 4th post-operative day and her latest CT thorax during follow up 2 years after operation did not show any tumour recurrence.

Discussion: The aim of chest wall reconstruction is to avoid instability and prevent thoracic organs from being exposed if the defect size is ≥10cm or at least three ribs are resected. Polypropylene mesh may be relatively weak in terms of mechanical support for the chest wall, however, in this case, the defect is not too large and the laterally reflected pectoral muscle can provide enough support together with the mesh.

Conclusion: Secondary chondrosarcoma in a young Asian female arising from a benign solitary enchondroma in the absence of multiple enchondromatosis, such as Ollier disease or Maffucci syndrome, is extremely rare. Regular follow up including physical assessment and radiological imaging can result in earlier detection of malignant transformation obviating the need for aggressive surgical treatment involving multiple rib resections.

Keywords: Asian; Case reports; Chondrosarcoma; Enchondroma; Female.

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Figures

Fig. 1
Fig. 1
Comparison of chest radiographs of patient in 2006 (left) and 2013 (right).
Fig. 2
Fig. 2
Comparison of computed tomography of thorax of patient in 2006 (left) and 2013 (right), coronal cuts (above), axial cuts (below).
Fig. 3
Fig. 3
Lung window axial cut of computed tomography of thorax 2013.
Fig. 4
Fig. 4
Gross image of resected chondrosarcoma (showing lesion posteriorly).
Fig. 5
Fig. 5
Histopathological findings of chondrosarcoma with soft tissue invasion.
Fig. 6
Fig. 6
Histopathological findings of chondrosarcoma medium with grade 1–2 cytological features.

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