Nakashima, Y., Unni, K.K., Shives, T.C., et al. (1986) Mesenchymal Chondrosarcoma of Bone and Soft Tissue: A Review of 111 Cases. Cancer, 57, 2444-2453.
http://dx.doi.org/10.1002/1097-0142(19860615)57:12<2444::AID-CNCR2820571233>3.0.CO;2-K

has been cited by the following article:

• TITLE: Mesenchymal Chondrosarcoma of the Infratemporal Fossa—A Rare Case Report

  AUTHORS: Shalender Sharma, J. K. Dayashankara Rao, Harsh Jain, Kaberi Majumder, Neelima Gehlot

  KEYWORDS: Chondrosarcoma; Mesenchymal Chondrosarcoma; Bone Neoplasm

  JOURNAL NAME: International Journal of Clinical Medicine, Vol.5 No.6, March 28, 2014

  ABSTRACT: Chondrosarcoma is a malignant neoplasm that results in abnormal bone and cartilage growth. Although Chondrosarcoma is rare, it is the second most common primary bone malignancy. Mesenchymal Chondrosarcoma (MCS) is a rare histological variant of Chondrosarcoma (CS) that accounts for only 1% of all CS and has high predilection for the head and neck region with a peak incidence in 2nd and 3rd decade of life. There is comparable male to female ratio with two thirds of the cases arising from bone and one third from soft tissue. The tumor is unique because of its aggressive growth with a high tendency for late recurrence and delayed metastasis. We present a case of this highly malignant lesion arising from the infratemporal fossa and rapidly involving maxillary tuberosity and mandibular ramus.