نتایج جستجو برای: retroperitoneal neoplasm

تعداد نتایج: 190474  

2015
V. Venkatarami Reddy S. Sarala Varughese Mathai Sreedhar Babu

Synovial sarcoma is a well-recognized malignant mesenchymal neoplasm. Primary retroperitoneal synovial sarcoma is extremely rare and has poor prognosis. There are sparse reports in the literature on the secretory synovial sarcomas. In this report, we present the case of a patient with retroperitoneal synovial sarcoma who presented with recurrent attacks of hypoglycaemia.

2016
Aydah Alawadhi Laszlo Leb

Multiple myeloma, a plasma cell neoplasm, presents most commonly with anemia, hypercalcemia, renal failure, and bone pain. Only few cases of clinical aggressive presentation associated with bleeding were reported in the medical literature. The reported cases included gastrointestinal bleeding and cardiac tamponade. Spontaneous retroperitoneal haemorrhage as initial presentation has not been so ...

Journal: :acta medica iranica 0
hayedeh haeri department of pathology, cancer institute, imam khomeini medical complex, tehran, iran. babak vosooghi department of pathology, cancer institute, imam khomeini medical complex, tehran, iran. fahimeh asadi amoli department of pathology, farabi hospital, tehran, iran.

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, ...

Journal: :Urology 1975
M Kalish R Dorr P Hoskins

A case of a large retroperitoneal tumor in a previously asymptomatic twenty-two-year-old white female is presented. A review of the literature confirms the rarity of this tumor. Its histologic and embryologic derivation as well as its subtle and bizarre method of presentation are discussed. The cause of such lesions is debatable, but primary cure can be accomplished by meticulous excision of th...

2015
Jun Yang Qin-qing Li Ying-ying Ding Liao Cheng-de

Thymoma is an epithelial neoplasm of the thymus, which commonly lies in the anterior mediastinum and recurrences of thymoma generally are locally, and retroperitoneal recurrence is considered to be rare. A 46-year old Asian woman with invasive thymoma had undergone thymectomy 10 years ago. Computed tomography demonstrated a well-circumscribed mass in the left retroperitoneal space. The patient ...

Journal: :The archives of bone and joint surgery 2014
Asieh Sadat Fattahi Godratollah Maddah Mohammad Motamedolshariati Taghi Ghiasi-Moghadam

Abdominal cystic lymphangioma is a rare benign neoplasm. Less than 1% of lymphangiomas is in the retroperitoneum. Lymphangioma is mostly asymptomatic. Chronic symptoms were reported in retroperitoneal type more than others. Acute symptoms due to complications like infection, cyst rupture or hemorrhage may occur. We report an 18-years-old girl with low back pain from 6 months ago with huge pelvi...

Journal: :The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology 2015
Türker Acar Duran Efe Ahmet Okuş İrfan Öcal Mustafa Harman

Retroperitoneal E-GIST is a very rare tumor and a total of 58 cases have been reported in the literature (2). The distinction of E-GIST from gastrointestinal stromal tumors (GIST) is made by proving the origin outside the alimentary system and ruling out a concurrent neoplasm in the gastrointestinal tract. In this letter, we aimed to report a very rare form of E-GIST arising from the retroperit...

2012
Saurabh Jain Souvik Chatterjee Jyoti Ranjan Swain Pritha Rakshit Partha Chakraborty Santanu Sinha

Castleman's disease is a rare nonclonal proliferative disorder of the lymph nodes with an unknown etiology. Common locations of Castleman's disease are mediastinum, neck, axilla, and abdomen. Castleman's disease of a peripancreatic location masquerading as pancreatic neoplasm is an even rarer entity. On search of published data, we came across about 17 cases published on peripancreatic Castlema...

Journal: :Tumori 2007
Tommaso Cioppa Daniele Marrelli Alessandro Neri Valeria Malagnino Stefano Caruso Enrico Pinto Franco Roviello

Primary osteosarcoma of the kidney is a very rare neoplasm with a very poor prognosis and unclear histogenesis. Only 20 cases have been reported in the literature. It has a strong tendency to recur locally and spread to distant sites. We present the clinical case of a 79-year-old man affected by a primary osteosarcoma of the kidney presenting with substantial retroperitoneal tumor hemorrhage. L...

2012
C Corbellini A Vingiani F Maffini A Chiappa E Bertani B Andreoni

The neurofibroma is a tumour of neural origin. This kind of neoplasm, though, is generally skin located. Rare cases in deep organs or in the peritoneal cavity are also reported in the literature. There are two types of neurofibromas, localized and diffuse; the latter is associated with von Recklinghausen disease and always occurs together with skin neurofibromas. Here we report the case of a 47...

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