نتایج جستجو برای: retroperitoneal neoplasm

تعداد نتایج: 190474  

2017
Yajie Yu Chao Liang Meiling Bao Pengfei Shao Zengjun Wang

BACKGROUND Currently, the standard treatment for renal pelvis carcinoma is radical nephroureterectomy with bladder cuff excision. To describe the feasibility of retroperitoneal laparoscopic partial nephrectomy with segmental renal artery clamping for cancer of renal pelvis, we report this special case for the first time. CASE PRESENTATION A 67-year-old woman received this operation. Preoperat...

Journal: :World Journal of Surgical Oncology 2005
Suresh VS Attili C Rama Chandra Dadhich K Hemant Poonamalle P Bapsy Clementeena RamaRao G Anupama

BACKGROUND Inflammatory myofibroblastic tumor (IMT) is a neoplasm of unknown etiology occurring at various sites. By definition, it is composed of spindle cells (myofibroblasts) with variable inflammatory component, hence the name is IMT. CASE PRESENTATION The present case is of a 46 years old woman presented with a history of flank pain, abdominal mass and intermittent hematuria for last 6 m...

2014
Christopher A. Behr Anthony J. Hesketh Samuel Z. Soffer Morris C. Edelman Richard D. Glick

Primary retroperitoneal mucinous cystadenomas are uncommon tumors whose incidence in the pediatric population is very low. We present the case report of a 17-year-old female with a primary retroperitoneal mucinous cystadenoma, borderline type, and describe the successful laparoscopic resection of the mass. 2014 The Authors. Published by Elsevier Inc. Open access under CC BY-NC-SA license. Prima...

2011
Armin Kamyab Michael John Jacobs

Introduction: Meningiomas and retroperitoneal sarcomas are two distinct rare tumors, with an incidence of 2 and 0.4 cases per 100,000 respectively. Case Report: We report the case of a 39 year old woman with a history of intracranial meningioma who was found two months later to have a large retroperitoneal sarcoma on CT scan after presenting to the emergency department complaining of abdominal ...

2017
Soheila Zareifar Sezaneh Haghpanah Mohammad Reza Farahmandfar

Background: Abdominal tumors are still a diagnostic problem in children. This study was conducted to assess the presentation and types of childhood intra abdominal tumors in children in Shiraz. Materials and Methods: Participants of this historical cohort study consisted of 298 children aged between 1.5 months to 15 years old who were diagnosed with abdominal mass between March 2003 and March 2...

Journal: :MOJ Public Health 2022

Malignant rhabdoid tumour is a very rare neoplasm with high lethality rate. Its neoplastic cells present rhabdomyoblastic features, although those must be differentiated from epithelioid sarcoma, melanoma, and rhabdomyosarcoma. Therefore, this case report of 21-year-old man who presented Malignantrhabdoid in the head pancreas. Patient was submitted to partial pancreatomy gastrectomy block, sple...

Journal: :Acta medica Iranica 2014
Hayedeh Haeri Babak Vosooghi Fahimeh Asadi Amoli

Primary retroperitoneal mucinous tumor (PRMT) of low malignant potential (border line) is an uncommon neoplasm with fewer than 50 reported cases. Uncertain diagnostic imaging results make diagnosis of its origin difficult, preoperatively. Later treatment planning and prognosis would be affected by exact diagnosis of the tumor origin. This study presents a case of Persian woman with diagnostic, ...

2016
Takehiro Maki Syotaro Fujino Kenjiro Misu Hiroyuki Kaneko Hitoshi Inomata Makoto Omi Masatoshi Tateno Kazuyoshi Nihei

Solitary fibrous tumor (SFT) is a rare stromal neoplasm and usually occurs in the thoracic cavity. We here report a case of retroperitoneal SFT with prominent calcification. A 64-year-old man presented with an incidentally detected retroperitoneal mass in the right upper abdomen. Imaging tests indicated an integrally calcified mass. The lesion was observed for 2 years and laparoscopically resec...

2017
Frederico José Ribeiro Teixeira Sergio Dias do Couto Netto André Luis de Freitas Perina Fabio C. M. Torricelli Luciana Ragazzo Teixeira Antonio Eduardo Zerati Fabio de Oliveira Ferreira Eduardo Hiroshi Akaishi William Carlos Nahas Edivaldo Massazo Utiyama

Leiomyosarcoma (LMS) of inferior vena cava (IVC) is a rare neoplasm affecting approximately 1/100,000 people. The prognosis is poor and potential curative intent occurs through challenging operations, such as vena cava resection, occasionally multivisceral when required, and vascular reconstruction. There are few retrospective series regarding this retroperitoneal neoplasm, and the aim of the p...

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