A connective tissue neoplasm or connective tissue tumor is a neoplasm arising from the tissues of the connective tissue[1]. (Not all tumors in the connective tissue are of the connective tissue.)
References
^Zelger, Bernhard (2002). "Connective tissue tumors". Recent Results in Cancer Research. Fortschritte Der Krebsforschung. Progres Dans Les Recherches Sur Le Cancer. 160: 343–350. doi:10.1007/978-3-642-59410-6_39. ISSN 0080-0015. Retrieved 21 November 2019.
External links
Classification
D
MeSH: D009372
v
t
e
Connective/soft tissue tumors and sarcomas (ICD-O 8800–9059) (C45–C49/D17–D21, 171/214–215)
Robot-assisted radical nephrectomy for primary renal mesenchymal chondrosarcoma: case report and literature review.
Deng W, Zhou J, Liu X, Chen L, Guo G, Fu B.
Renal failure. 2019 Nov;41(1)98-103.
As an extremely rare malignant neoplasm, only 12 mesenchymal chondrosarcoma (MC) arising in kidney have been reported to date. Herein, we reported a case of primary renal MC resected with robot assistance, which has not been reported before. According to the cases reported in English literature, we
Polydopamine-based surface modification of paclitaxel nanoparticles for osteosarcoma targeted therapy.
Zhao L, Bi D, Qi X, Guo Y, Yue F, Wang X, Han M.
Nanotechnology. 2019 Jun;30(25)255101.
In order to achieve the purpose of targeting treatment of osteosarcoma, we developed novel paclitaxel (PTX) nanoparticles (Nps) coated with polydopamine (PDA) and grafted by alendronate (ALN) as ligand. Dopamine can be easily polymerized on various surfaces to form a thin PDA film in alkaline enviro
Alveolar soft-part sarcoma: can MRI help discriminating from other soft-tissue tumors? A study of the French sarcoma group.
Crombé A, Brisse HJ, Ledoux P, Haddag-Miliani L, Bouhamama A, Taieb S, Le Loarer F, Kind M.
European radiology. 2019 Jun;29(6)3170-3182.
To investigate the imaging features of alveolar soft-part sarcomas (ASPS) on pre-treatment MRI in order to identify relevant criteria to distinguish ASPS from other soft-tissue tumors. A series of 25 patients (mean age, 18.5 years old) with histologically proven ASPS from five French comprehensive