نتایج جستجو برای: sarcoma

تعداد نتایج: 74250  

2012

Extraskeletal Ewing’s Sarcoma is a rare soft tissue tumor that is morphologically indistinguishable from the more common Ewing’s sarcoma of the bone. Primitive Ewing’s sarcoma of the breast is exceptionally reported. We present the case of a 26-year-old woman with Ewing sarcoma/PNET diagnosed by molecular biology showing the specific t ranscr ipt of Ewing/ per ipheral pr imi t ive neuroectoderm...

2016
Jisook Yoo Mingyul Jo Min-Soo Kim Kwang-Hyun Choi Hyang-Joon Park Mihn-Sook Jue

Kaposi's sarcoma is a multifocal proliferative vascular tumor involving the skin and other organ and psoriasis is a chronic cutaneous disease with papules and plaques with white scale. Development of Kaposi's sarcoma in psoriasis patients has been reported rarely. A 71-year-old man presented with multiple brownish to violaceous plaques on both feet and arms which were found 4 months ago. The bi...

Journal: :Sarcoma 1998
Martin H. Robinson Raphael E. Pollock

Dr Robinson is Senior Lecturer in Clinical Oncology, in the Section of Clinical Oncology, at Weston Park Hospital, Shef® eld, UK. He has been involved in the ® eld of sarcomas for 10 years and runs a sarcoma clinic at the above hospital. His other main area of interest is the treatment of head and neck cancer. He is chairman of the Local Treatment Group of the EORTC Soft Tissue and Bone Sarcoma...

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2008
Lesley A Anderson Carmela Lauria Nino Romano Elizabeth E Brown Denise Whitby Barry I Graubard Yan Li Angelo Messina Lorenzo Gafà Francesco Vitale James J Goedert

BACKGROUND Classical Kaposi sarcoma is a rare complication of Kaposi sarcoma-associated herpes virus (KSHV) infection. We conducted a population-based, frequency-matched case-control study in Sicily to further investigate the reported inverse relationship between smoking and classical Kaposi sarcoma and to identify other factors associated with altered risk. METHODS All incident, histological...

2014
Tomonori Nagai Yasushi Takai Taichi Akahori Hiroaki Ishida Tatsuya Hanaoka Takahiro Uotani Sho Sato Shigetaka Matsunaga Kazunori Baba Hiroyuki Seki

Preoperative diagnosis of uterine sarcoma is very difficult, and currently, its diagnostic accuracy is not satisfactory. It is therefore important to perform surgery and establish the pathological diagnosis if the clinical findings and various examination findings indicate possible uterine sarcoma. We investigated the accuracy of the combination of various types of predictors of uterine sarcoma...

Journal: :Annals of Surgical Oncology 2021

Pulmonary metastasectomy for sarcoma is surgery without proven benefit, and in the light of a randomized controlled trial examining pulmonary colorectal cancer, it should be questioned.

2011

Fibrosarcoma of lw.uflHistiocytosis X .~ -.lc..ltl Neurilemmoma of "'t<• d,i,[L Giant Cell Tumor .f .u.t..ht~ Osteogenic Sarcoma of Cw ~~!lFibrous Dysplasia o{ lVi b Giant Cell Tumor J. !MovPChondrosarcoma o( thv,.., Chondromyxoid Fibroma of h':>u\~ Osteoid Osteoma :fr \RN•uil Undifferentiat.ed Grade 4 Sarcoma of ;liv"' Etdng 1 s Sarcoma ~ ('~"~~ Desmoid :k I~ M;yositis Ossificans ~ l{....f Mal...

Journal: :Journal of gynecologic oncology 2010
Azamsadat Mousavi Setare Akhavan

Sarcoma botryoides (embryonal rhabdomyosarcoma) rarely arises in the uterine cervix. We report a case of a 14-year-old female with sarcoma botryoides who presented with prolonged vaginal bleeding and cervical polyp. The biopsy specimen confirmed sarcoma botryoides. The patient underwent radical surgery of the tumor and hysterectomy without adjuvant chemotherapy. The sister of the patient had di...

Journal: :Revista de la Facultad de Medicina 2021

Introduction: Alveolar soft part sarcoma is a very rare and aggressive type of sarcoma. Although its histology genetic characteristics have been identified, the benefits adjuvant radiotherapy for treatment are still being studied. Case presentation: In November 2007, 21-year-old woman presented with primary tumor in right thigh, histological immunohistochemical confirmation an alveolar sarcoma,...

2011
Beverly A. Teicher Rebecca G. Bagley Cecile Rouleau Ariel Kruger Yi Ren Leslie Kurtzberg

Ewing/PNET (peripheral neuroepithelioma) tumors are rare aggressive bone sarcomas occurring in young people. Rare-disease clinical trials can require global collaborations and many years. In vivo models that as accurately as possible reflect the clinical disease are helpful in selecting therapeutics with the most promise of positive clinical impact. Human Ewing/PNET sarcoma cell lines developed...

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