نتایج جستجو برای: retroperitoneal tumors

تعداد نتایج: 185857  

Journal: :Bakirkoy Tip Dergisi / Medical Journal of Bakirkoy 2019

2008
Ralf-Bodo Tröbs Christian Geyer Wolfgang Hirsch Andrea Tannapfel

We report on two infants of 11 and 12 months of age, respectively, with large solid-cystic retroperitoneal tumors. Complete resection was achieved, and both children are doing well over a follow-up of more than 17 months. The presented paper focuses on surgical anatomy of this very rare type of tumor. Teratomas were located mainly within the upper abdominal cavity, and both tumors displaced the...

Journal: :Journal of surgery and medicine 2022

Follicular dendritic cell sarcomas (FDCS) are spindle lesions that large, slow-growing masses in either nodal or extranodal regions both and originate from B-cell follicles of the lymph nodes. Most tumors cervical nodes, but retroperitoneal mediastinal origins have also been reported. Extranodal areas include soft tissues, skin, tonsils, gastrointestinal tract, liver, spleen. The spleen is an u...

Journal: :medical journal of islamic republic of iran 0
b geramizadeh from the transplant research center, nemazee hospital. shiraz university a/medical sciences. shiraz. iran. a azizi pv kumar hr forootan a rasekhi

the aim of this study was to evaluate the role of fine needle aspiration cytology in the diagnosis of abdominal and retroperitoneal masses in children on this study. in 53 cases of childhood abdominal and retroperitoneal masses within a 4 year period (1998- 2001) preoperative fine needle aspiration was done under the guide of ct scan. 2 pathologists reviewed fine needle aspiration smears. in al...

Journal: :Urologia internationalis 1995
A Stein E Aghai O Cohen Z Shapira A Lurie

Large-cell retroperitoneal lymphoma was partially resected including a long segment of ureter. The proximal end of the ureter was clipped during surgery. A percutaneous nephrostomy was inserted after 48 h. Adjuvant chemotherapy was then delivered and the kidney was autotransplanted to the contralateral iliac fossa. Salvage of a hydronephrotic functioning kidney by nephrostomy and delayed contra...

2015
Susan J. Hall Simon T. Williams Trevor A. Jackson Agnes T.F. Lee Tom A. McCulloch

Retroperitoneal schwannomas are extremely rare, and unreported in Urology. Often thought to be malignant from imaging the diagnosis is often delayed until Histology. We report a case of retroperitoneal schwanoma thought to be a malignant renal mass. Seventy three year old lady presented with abdominal pain. Imaging showed a mass attached to the renal pelvis thus she underwent a radical nephrect...

Journal: :Sarcoma 2000
Michael Froehner Hans-Juergen Gaertner Andreas Manseck Sven Oehlschlaeger Manfred P. Wirth

Patient. A 65-year-old man was admitted with a large primary retroperitoneal tumor and an increased beta-human chorionic gonadotropin (beta-HCG) serum level. A germ cell tumor was suspected; however, a computed tomography-guided biopsy failed to enable tumor classification. After two courses of chemotherapy, the beta-HCG serum level had returned to the normal level and a diagnostic laparotomy w...

2015
Mayank Tripathi Sanjeev Parshad Rajender Kumar Karwasra Ashish Gupta Saket Srivastva Ankush Sarwal

Background. Retroperitoneal lymphangioma is a rare, benign mesodermal tumor arising from the retroperitoneal lymphatics which usually presents in infancy and it is worthy to report a case when it has presented in an adult. After a thorough literature search in English we concluded that less than 200 cases of adult retroperitoneal lymphangioma have been reported so far. Apart from being a rare e...

2016
Erica C. Prochaska Andrew P. Sciallis Barbra S. Miller

Establishing the etiology of a retroperitoneal tumor may be difficult due to close proximity of multiple organs. Evaluation of retroperitoneal tumors often leads to surgery, many times to obtain a definitive diagnosis and rule out malignancy. Calcifying fibrous tumors (CFT) are very rare soft tissue tumors occurring most often in young patients. They are most often found arising in the thoracic...

2014
Esat Korgali Gokce Dundar Gokhan Gokce Fatih Kilicli Sahande Elagoz Semih Ayan Emin Yener Gultekin

Pheochromocytoma is a rare and usually benign neuroendocrine neoplasm. Only 10% of all these tumors are malignant and there are no definitive histological or cytological criteria of malignancy. Single malignancy criteria are the presence of advanced locoregional disease or metastases. We report a case, with a giant retroperitoneal tumor having multiple metastases including palpable rib metastas...

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