Chondrosarcoma

Chondrosarcoma is a malignant bone tumor arising from cartilaginous tissue, most frequently occuring at the ends of the femur and tibia, the proximal end of the humerus and the pelvis; and presenting with a palpable mass and progressive pain. Chondrosarcoma is usually slow growing at low histological grades and can be well managed by intralesional curettage or en-block wide resection.

Sarcoma

A connective tissue neoplasm formed by proliferation of mesodermal cells. Bone and soft tissue sarcomas are the main types of sarcoma. Sarcoma is usually highly malignant.

Total: 129

(per page)

PMID (PMCID)
31020273	OTHER
	A rare case of TLE1-positive sclerosing epithelioid fibrosarcoma expanding the differential diagnosis of TLE1-positive tumors: a case report.
	Perez D, Fullmer JM, Naous R. AME Case Rep. 2019;3:6.
	Occasional weak staining for TLE1 has also been described in clear cell sarcoma, high-grade chondrosarcoma, Ewing sarcoma, rhabdomyosarcoma, GIST, myxofibrosarcoma, and leiomyosarcoma.
31007495	OTHER
	Anaplastic sarcoma of the kidney: Case report and literature review.
	Chen CC, Liao KS. Ci Ji Yi Xue Za Zhi. 2019;31(2):129-132.
	The differential diagnoses included anaplastic sarcoma of the kidney (ASK), anaplastic Wilms tumor, mesenchymal chondrosarcoma, sarcomatoid renal cell carcinoma, clear cell sarcoma of the kidney, rhabdoid tumor of the kidney, congenital mesoblastic nephroma, and synovial sarcoma.
31007495	OTHER
	Anaplastic sarcoma of the kidney: Case report and literature review.
	Chen CC, Liao KS. Ci Ji Yi Xue Za Zhi. 2019;31(2):129-132.
	The differential diagnoses included anaplastic sarcoma of the kidney (ASK), anaplastic Wilms tumor, mesenchymal chondrosarcoma, sarcomatoid renal cell carcinoma, clear cell sarcoma of the kidney, rhabdoid tumor of the kidney, congenital mesoblastic nephroma, and synovial sarcoma.
31001441	OTHER
	Low-Grade Chondrosarcoma of the Proximal Phalanx: A Rare Presentation.
	Knapp P, Aviles A, Najarian C. Case Rep Orthop. 2019;2019:6402979.
	Chondrosarcomas are the second most common primary malignant sarcoma of the bone, though it is overall a rare tumor.
30819134	FEMALE	Child
	Primary paediatric epidural sarcomas: molecular exploration of three cases.
	Low SYY, Kuick CH, Seow WY, Bte Syed Sulaiman N, Chen H, Lian DWQ, Chang KTE, Tan EEK, Soh SY, Tan GIL, Ng LP, Seow WT, Low DCY. BMC Cancer. 2019;19(1):182.
	We report the molecular exploration of 3 primary paediatric epidural sarcomas-one in the cranium (mesenchymal chondrosarcoma) and 2 in the spine (mesenchymal chondrosarcoma and Ewing sarcoma respectively).
30819134	FEMALE	Child
	Primary paediatric epidural sarcomas: molecular exploration of three cases.
	Low SYY, Kuick CH, Seow WY, Bte Syed Sulaiman N, Chen H, Lian DWQ, Chang KTE, Tan EEK, Soh SY, Tan GIL, Ng LP, Seow WT, Low DCY. BMC Cancer. 2019;19(1):182.
	We report the molecular exploration of 3 primary paediatric epidural sarcomas-one in the cranium (mesenchymal chondrosarcoma) and 2 in the spine (mesenchymal chondrosarcoma and Ewing sarcoma respectively).
30274851	OTHER
	Self limiting sternal tumors of childhood: two case reports.
	Adri D, Kreindel T. Radiologia. 2019;61(2):167-170.
	The differential diagnoses include a wide spectrum of benign (from bone cyst to osteoblastoma, osteochondroma and fibrous displasia) and malignant tumours (Ewing's sarcoma, chondrosarcoma rhabdomyosarcoma), inflammatory lesions and infectious processes.
29491605 (5824517)	OTHER
	Aggressive high-grade Ewing's sarcoma of maxilla: A rare case report.
	Yogesh TL, Shetty A, Keswani H, Rishi D. J Oral Maxillofac Pathol. 2018;22(Suppl 1):S48-S53.
	Ewing's sarcoma (ES) is an uncommon malignancy of childhood and adults that constitutes 6%-8% of all primary malignant tumors and the third-most common tumor after osteosarcoma and chondrosarcoma, frequently involves the mandible among jaw bones.
30181407	MALE
	Clear cell chondrosarcoma of the larynx.
	Hendriks T, Cardemil F, Sader C. BMJ Case Rep. 2018;2018:.
	Chondrosarcomas are the most common type of sarcoma in the larynx but the CCC variant is rare.
30450218 (6236490)	OTHER
	Invasive nasal histiocytic sarcoma as a cause of temporal lobe epilepsy in a cat.
	Santifort KM, Jurgens B, Grinwis GC, Gielen I, Meij BP, Mandigers PJ. JFMS Open Rep. 2018;4(2):2055116918811179.
	Other differential diagnoses are primary nasal neoplasia (eg, adenocarcinoma, squamous cell carcinoma, chondrosarcoma and other types of sarcomas), lymphoma and olfactory neuroblastoma.
28852958 (5574947)	MIXED_SAMPLE	Adult
	Clinical benefit of antiangiogenic therapy in advanced and metastatic chondrosarcoma.
	Jones RL, Katz D, Loggers ET, Davidson D, Rodler ET, Pollack SM. Med Oncol. 2017;34(10):167.
	A retrospective search of patients treated at three sarcoma referral centers was performed to identify patients with advanced chondrosarcoma treated with antiangiogenic agents.
28648942	MALE	Middle Aged
	Dedifferentiated chondrosarcoma of bone with prominent rhabdoid component.
	Stemm M, Beck C, Mannem R, Neilson J, Klein MJ. Ann Diagn Pathol. 2017;28:7-11.
	Dedifferentiated chondrosarcomas (DDCS) are rare lesions, defined as tumors having a low-grade chondrosarcomatous component with an abrupt transition to a high-grade sarcoma.
29232802	MALE
	[Sarcomatoid Urothelial Carcinoma of the Bladder Including an Osteosarcoma Element].
	Tanuma K, Kawai K, Tsuchiya H, Matsumoto Y, Kandori S, Kojima T, Kimura T, Joraku A, Miyazaki J, Nishiyama H, Sakata A. Hinyokika Kiyo. 2017;63(11):487-492.
	Histologically, the non-papillary part was composed of sarcomatous elements including osteosarcoma, chondrosarcoma, and spindle cell sarcoma.
27102568	MIXED_SAMPLE	Child
	Critical reappraisal of primary osseous composite sarcoma (malignant mesenchymoma) - analysis of four cases and literature review.
	Chow LT. APMIS. 2016;124(6):487-99.
	In accordance with recent terminology, it is proposed that malignant mesenchymoma should be renamed 'composite sarcoma' and defined as 'a sarcoma composed of two or more cellular types each of which is sufficiently differentiated to permit clear recognition of its histogenetic type microscopically, immunohistochemically or ultrastructurally; excluding fibrosarcomatous and high-grade pleomorphic undifferentiated sarcomatous component, dedifferentiated sarcoma and the combination of osteosarcoma and chondrosarcoma which is regarded as a single histogenetic type'.
27102568	MIXED_SAMPLE	Child
	Critical reappraisal of primary osseous composite sarcoma (malignant mesenchymoma) - analysis of four cases and literature review.
	Chow LT. APMIS. 2016;124(6):487-99.
	In accordance with recent terminology, it is proposed that malignant mesenchymoma should be renamed 'composite sarcoma' and defined as 'a sarcoma composed of two or more cellular types each of which is sufficiently differentiated to permit clear recognition of its histogenetic type microscopically, immunohistochemically or ultrastructurally; excluding fibrosarcomatous and high-grade pleomorphic undifferentiated sarcomatous component, dedifferentiated sarcoma and the combination of osteosarcoma and chondrosarcoma which is regarded as a single histogenetic type'.
27102568	MIXED_SAMPLE	Child
	Critical reappraisal of primary osseous composite sarcoma (malignant mesenchymoma) - analysis of four cases and literature review.
	Chow LT. APMIS. 2016;124(6):487-99.
	In accordance with recent terminology, it is proposed that malignant mesenchymoma should be renamed 'composite sarcoma' and defined as 'a sarcoma composed of two or more cellular types each of which is sufficiently differentiated to permit clear recognition of its histogenetic type microscopically, immunohistochemically or ultrastructurally; excluding fibrosarcomatous and high-grade pleomorphic undifferentiated sarcomatous component, dedifferentiated sarcoma and the combination of osteosarcoma and chondrosarcoma which is regarded as a single histogenetic type'.
27644571	MIXED_SAMPLE	Adult
	Delayed Diagnosis of Primary Bone and Soft Tissue Tumors Initially Treated as Degenerative Spinal Disorders.
	Nishisho T, Sakai T, Tezuka F, Higashino K, Takao S, Takata Y, Miyagi R, Toki S, Abe M, Yamashita K, Nagamachi A, Sairyo K. J Med Invest. 2016;63(3-4):274-7.
	Three patients had a malignant tumor (osteosarcoma, chondrosarcoma, or small round cell sarcoma) at the progressive stage, and 1 died of lung metastasis.
27163097 (4849246)	OTHER
	Paraneoplastic vasculitis associated to pelvic chondrosarcoma: a case report.
	Arvinius C, Gonzalez-Perez A, Garcia-Coiradas J, Garcia-Maroto R, Cebrian-Parra JL. SICOT J. 2016;2:8.
	We report a case of a 45-year-old female patient with pelvic chondrosarcoma who underwent surgical treatment and started to present visual loss, systemic inflammatory response syndrome (SRIS), cardiac insufficiency, hepatosplenomegaly, cholestasis as well as pulmonary bleeding suggesting a sarcoma-associated vasculitis.
26537339 (4632365)	FEMALE	Adult
	Implantation of customized 3-D printed titanium prosthesis in limb salvage surgery: a case series and review of the literature.
	Fan H, Fu J, Li X, Pei Y, Li X, Pei G, Guo Z. World J Surg Oncol. 2015;13:308.
	Three patients with clavicle Ewing's sarcoma (ES), scapular ES, and pelvic chondrosarcoma (CS) were scanned by computer tomography (CT).
25663866 (4315059)	OTHER
	Rare chondrosarcoma of the breast treated with quadrantectomy instead of mastectomy: A case report.
	Pasta V, Sottile D, Urciuoli P, Del Vecchio L, Custureri F, D'Orazi V. Oncol Lett. 2015;9(3):1116-1120.
	Breast chondrosarcoma is a rare sarcoma that mainly occurs in females >50 years old.