SM Journal of Sarcoma Research is an open access peer reviewed journal publishing articles committed to provide significant information on Sarcoma Immunotherapy, Improved drug delivery, new drugs, Targeted therapy, Targeted oncogene treatments, Tumor genetics, Palliative care/supportive care, etc. Our experienced team of experts provides editorial excellence, rapid publication, and high visi...Readmore |
Nocardiosis is a potentially lethal complication of organ transplantation. Each year, approximately 500 to 1000 cases of nocardiosis are diagnosed in the United States. Nocardiosis commonly occu... Download PDF
Christian Green*, Nicholas Palagonia, Brandon Watkins, Kollin Kahler, Mehuliben Upadhyaya, Jose Encarnacion, and Mohamed Aziz
Gastrointestinal stromal tumors (GISTs) are rare, making up less than 1% of all gastrointestinal tumors. Each year, approximately 4,000 to 6,000 adults in the United States will be diagnosed wit... Download PDF
Christian Green*, Nicholas Palagonia, Petr Stastka, Andrea Cevallos, Elizabeth O’Grady, Zachary Elder, and Mohamed Aziz
Giant cell tumors of the bone (GCTB), while often benign, are regarded as locally aggressive and highly unpredictable with the capability to recur, metastasize, and even undergo sarcomatous tran... Download PDF
Georgette Nader*, Hana Soueidan, Richard Danieli, Samuel Malek, Savanna Craib, Karina Leyva, Daniel Quinn and Mohamed Aziz
Mesenchymal chondrosarcomas (MC) are a rare and aggressive neoplasm characterized by primitive mesenchymal cells mixed with well differentiated islands of cartilage. MCs account for 2%-9% of all... Download PDF
Jason Comeau*, Andrew Kung, Andrew Treihaft, Jordan Gonia. Bailey Corona, Allison Parrill , Daniel Quinn, and Mohamed Aziz
Extraskeletal small cell osteosarcoma (ESCOS) is a rare tumor which may present a challenging primary diagnosis on cytologic assessment. The cytomorphology of this tumor is similar to other smal... Download PDF
Kollin Kahler*Alexander Garcia, Jenna Jarrell, Rona Bakri, Savanna Craib, Karina Leyva, Christian Green, and Mohamed Aziz
Extraskeletal Myxoid Chondrosarcomas (EMC) are rare low-grade malignant mesenchymal neoplasms of uncertain differentiation characterized by abundant myxoid matrix. EMCs account for almost 3% of ... Download PDF
Garrett Jackson*, Yassin Nayel, Joseph Varney, Yeonjoo Cho, Ngowari Pokima, Hong Yu Wang, and Mohamed Aziz
Immune checkpoint inhibitors revive pre-existing immune responses that are suppressed in cancer. To restore innate tumour surveillance that is lost in cancer patients, a tumoricidal agent may ha... Download PDF
Sant P Chawla, K Kumar Sankhala, Joshua R Ravicz, Grace E Kang, Seiya Liu, Nupur Assudani, Shiva Sreenath Andrali, Nathan Stumpf, Bryan C Leong, Seth Kim, Suzan Arasheben,William Tseng, Don A Brigham and Erlinda M Gordon*
Soft tissue sarcomas (Sts) are rare tumors that make up about 1% of malignant neoplasms. In addition to their histological diversity, Stscan occur anywhere on the body but present predominance i... Download PDF
Giselle Almeida* (ICAVC), Lucas Jacometo Coelho de Castilho (ICAVC), Gisele Aparecida da Costa Gonçalves Pires1 (ICAVC), Priscila Souza Schinzari (UNISA) and Isabela Moraes Bernal (UNISA)
Vincristine, ifosfamide, doxorubicin and etoposide (VIDE) is an intensive multiagent induction chemotherapy regimen used in the treatment of Ewing and other sarcoma, most often in children and y... Download PDF
Brandon Lau, Peter Grimison and Vivek BhadriZ*
Background: Myxoid Leiomyosarcoma (LMS) is a rare and aggressive subtype of soft tissue sarcoma. Currently the true incidence and prognosis of myxoid leiomyosarcoma is unknown. This study examin... Download PDF
Jonathan Gootee, Elida Voth, Christina Curtin, Peter Silberstein and Leah Grant*
Director, Interventional Implant Program
MedStar Heart & Vascular Institute,
Washington, DC, USA
This work is licensed under a Creative Commons Attribution 4.0 International License.
