Mesenchymal chondrosarcoma (MC) is a subtype of chondrosarcoma which is rarely encountered in the clinical practice. It carries a worse prognosis compared to other forms of chondrosarcoma as it has a high tendency to metastasize to other sites.1 It can arise from skeletal bone as well as soft tissue, the usual sites being the ribs and jaw.2 Histologically, it is characterized by a mix of cartilage and undifferentiated stromal tissue, which will be highly positive for S100. A survey done concluded that it commonly affects patients in their second or third decade of life.3 We will discuss a rare case of MC which presented to our center where the initial biopsy was reported as hemangiopericytoma (HPC) of nose. The tumour was excised using endoscopic assisted craniofacial resection (EACFR). A multidisciplinary team comprising of various specialties was involved in diagnosing and managing the patient.
Published in | International Journal of Otorhinolaryngology (Volume 1, Issue 1) |
DOI | 10.11648/j.ijo.20150101.13 |
Page(s) | 9-12 |
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This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
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Copyright © The Author(s), 2015. Published by Science Publishing Group |
Mesenchymal Chondrosarcoma, Sphenoid Sinus Tumour
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APA Style
Ahmad Kusyairi Bin Khalid, Haizlene Abd Halim, Balwant Singh Gendeh. (2015). A Rare Case of Sphenoid Sinus Mesenchymal Chondrosarcoma: A Diagnostic Challenge. International Journal of Otorhinolaryngology, 1(1), 9-12. https://doi.org/10.11648/j.ijo.20150101.13
ACS Style
Ahmad Kusyairi Bin Khalid; Haizlene Abd Halim; Balwant Singh Gendeh. A Rare Case of Sphenoid Sinus Mesenchymal Chondrosarcoma: A Diagnostic Challenge. Int. J. Otorhinolaryngol. 2015, 1(1), 9-12. doi: 10.11648/j.ijo.20150101.13
@article{10.11648/j.ijo.20150101.13, author = {Ahmad Kusyairi Bin Khalid and Haizlene Abd Halim and Balwant Singh Gendeh}, title = {A Rare Case of Sphenoid Sinus Mesenchymal Chondrosarcoma: A Diagnostic Challenge}, journal = {International Journal of Otorhinolaryngology}, volume = {1}, number = {1}, pages = {9-12}, doi = {10.11648/j.ijo.20150101.13}, url = {https://doi.org/10.11648/j.ijo.20150101.13}, eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ijo.20150101.13}, abstract = {Mesenchymal chondrosarcoma (MC) is a subtype of chondrosarcoma which is rarely encountered in the clinical practice. It carries a worse prognosis compared to other forms of chondrosarcoma as it has a high tendency to metastasize to other sites.1 It can arise from skeletal bone as well as soft tissue, the usual sites being the ribs and jaw.2 Histologically, it is characterized by a mix of cartilage and undifferentiated stromal tissue, which will be highly positive for S100. A survey done concluded that it commonly affects patients in their second or third decade of life.3 We will discuss a rare case of MC which presented to our center where the initial biopsy was reported as hemangiopericytoma (HPC) of nose. The tumour was excised using endoscopic assisted craniofacial resection (EACFR). A multidisciplinary team comprising of various specialties was involved in diagnosing and managing the patient.}, year = {2015} }
TY - JOUR T1 - A Rare Case of Sphenoid Sinus Mesenchymal Chondrosarcoma: A Diagnostic Challenge AU - Ahmad Kusyairi Bin Khalid AU - Haizlene Abd Halim AU - Balwant Singh Gendeh Y1 - 2015/09/14 PY - 2015 N1 - https://doi.org/10.11648/j.ijo.20150101.13 DO - 10.11648/j.ijo.20150101.13 T2 - International Journal of Otorhinolaryngology JF - International Journal of Otorhinolaryngology JO - International Journal of Otorhinolaryngology SP - 9 EP - 12 PB - Science Publishing Group SN - 2472-2413 UR - https://doi.org/10.11648/j.ijo.20150101.13 AB - Mesenchymal chondrosarcoma (MC) is a subtype of chondrosarcoma which is rarely encountered in the clinical practice. It carries a worse prognosis compared to other forms of chondrosarcoma as it has a high tendency to metastasize to other sites.1 It can arise from skeletal bone as well as soft tissue, the usual sites being the ribs and jaw.2 Histologically, it is characterized by a mix of cartilage and undifferentiated stromal tissue, which will be highly positive for S100. A survey done concluded that it commonly affects patients in their second or third decade of life.3 We will discuss a rare case of MC which presented to our center where the initial biopsy was reported as hemangiopericytoma (HPC) of nose. The tumour was excised using endoscopic assisted craniofacial resection (EACFR). A multidisciplinary team comprising of various specialties was involved in diagnosing and managing the patient. VL - 1 IS - 1 ER -