WordNet

a usually malignant tumor arising from connective tissue (bone or muscle etc.); one of the four major types of cancer
not differentiated (同)uniform

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1. 小児および思春期の横紋筋肉腫および未分化型肉腫：治療 rhabdomyosarcoma and undifferentiated sarcoma in childhood and adolescence treatment
2. 小児および思春期の横紋筋肉腫および未分化型肉腫：臨床症状、診断的評価、および
病期分類 rhabdomyosarcoma and undifferentiated sarcoma in childhood and adolescence clinical presentation diagnostic evaluation and staging
3. 小児および思春期の横紋筋肉腫および未分化型肉腫：疫学、病理、および分子学的病因 rhabdomyosarcoma and undifferentiated sarcoma in childhood and adolescence epidemiology pathology and molecular pathogenesis
4. 軟部組織肉腫の臨床所見、病理組織学的検査、診断的評価、および病期分類 clinical presentation histopathology diagnostic evaluation and staging of soft tissue sarcoma
5. 後腹膜軟部組織肉腫の臨床的特徴、評価、および治療 clinical features evaluation and treatment of retroperitoneal soft tissue sarcoma

A Rare Type of Secondary Cancer in a Child With Acute Lymphoblastic Leukemia: Malignant Fibrous Histiocytoma.

Incesoy Özdemir S, Balkaya E, Oren AC, Bozkurt C, Sahin G, Unlü RE, Ertem AU.Source*Department of Pediatric Oncology, Dr Sami Ulus Obstetrics and Pediatrics Training and Research Hospital †Department of Plastic Surgery, Ankara Numune Training and Research Hospital, Ankara, Turkey.
Journal of pediatric hematology/oncology.J Pediatr Hematol Oncol.2013 Oct 3. [Epub ahead of print]
Secondary cancers which are related with treatment of childhood acute lymphoblastic leukemia (ALL) is a significant problem with longer term. For development of secondary cancer after treatment, the latency period varies between 5 and 10 years. In this case, a 13 year-old-boy diagnosed as high-risk
PMID 24096378

McMillan RR, Sima CS, Moraco NH, Rusch VW, Huang J.SourceThoracic Service, Department of Surgery, Memorial Sloan-Kettering Cancer Center, New York, New York.
The Annals of thoracic surgery.Ann Thorac Surg.2013 Oct;96(4):1223-1228. doi: 10.1016/j.athoracsur.2013.05.015. Epub 2013 Jul 25.
BACKGROUND: Soft tissue sarcoma (STS) of the chest wall is uncommon, and our knowledge is limited to small, single institutional case series. Although some series have examined prognostic factors for survival with this rare set of neoplasms, our knowledge of the patterns of relapse is limited.METHOD
PMID 23891404

Uterine sarcoma-current management and experience from a regional cancer centre in North India.

Biswas A, Patel F, Kumar P, Srinivasan R, Bera A, Sharma SC, Rajwanshi A.SourceDepartment of Radiotherapy and Oncology, Postgraduate Institute of Medical Education and Research, Chandigarh, India, dr_ahitagni@yahoo.co.in.
Archives of gynecology and obstetrics.Arch Gynecol Obstet.2013 Oct;288(4):873-82. doi: 10.1007/s00404-013-2843-7. Epub 2013 Apr 12.
PURPOSE: We intended to assess the clinicopathological features and treatment outcome in patients of uterine sarcoma.METHOD: A retrospective review of medical records of patients of uterine sarcoma (2002-2007) was conducted. Overall survival (OS) was analyzed by Kaplan-Meier method.RESULTS: Forty-tw
PMID 23580012

High-grade undifferentiated pleomorphic sarcoma of pelvis treated with curettage and bone graft after complete remission following caffeine-potentiated chemotherapy

Tsuchiya Hiroyuki,Takeuchi Akihiko,Yamamoto Norio,Shirai Toshiharu,Hayashi Katsuhiro,Nishida Hideji,Tomita Katsuro
Journal of Orthopaedic Science 16(4), 476-481, 2011-07
NAID 120003497600

High-grade undifferentiated pleomorphic sarcoma of pelvis treated with curettage and bone graft after complete remission following caffeine-potentiated chemotherapy

Tsuchiya Hiroyuki,Takeuchi Akihiko,Yamamoto Norio,Shirai Toshiharu,Hayashi Katsuhiro,Nishida Hideji,Tomita Katsuro
Journal of Orthopaedic Science 16(4), 476-481, 2011-07
NAID 120003002569