scholarly journals A vena cava inferiorból kiinduló primer leiomyosarcoma esete

2019 ◽  
Vol 160 (19) ◽  
pp. 756-761
Author(s):  
Csaba Weninger ◽  
Edit Várady ◽  
Giyab Omar ◽  
Imre Szabó ◽  
Tamás Tornóczky

Abstract: The venous invasion from intraabdominal and retroperitoeal tumors (e.g., liver and kidney) is relatively frequent. Primary vascular (venous) tumors are uncommon. The authors review the case of a 67-year-old woman, who was admitted to the hospital in a poor general condition with jaundice. Laboratory findings indicated hepatic and renal insufficiency. Abdominal ultrasound detected a large retroperitoneal mass which was suspected to be of uterine origin. Abdominal CT showed a retroperitoneal mass that invaded the inferior vena cava, but there was no sign of primary intraabdominal or pelvic tumor. Due to the poor general condition of the patient, surgery was not performed. The patient died in some days after admission. Autopsy revealed a primary leiomyosarcoma of the inferior vena cava. Based on the literature data, primary leiomyosarcoma of the inferior vena cava is extremely rare. Leiomyosarcoma of the inferior vena cava can cause various symptoms, depending on the involved segment of the vein. Surgical intervention can be performed in early stages of the disease. In uncertain retroperitoneal tumors involving the inferior vena cava, radiologists should think of the possibility of tumor with vascular origin. Orv Hetil. 2019; 160(19): 756–761.

Pathobiology ◽  
1961 ◽  
Vol 24 (1) ◽  
pp. 72-76 ◽  
Author(s):  
A. Laufer ◽  
J. Plaschkes

2008 ◽  
Vol 34 (6) ◽  
pp. 720-724 ◽  
Author(s):  
M. Fiore ◽  
P. Locati ◽  
C. Mussi ◽  
A. Guarino ◽  
L. Piva ◽  
...  

2014 ◽  
Vol 04 (04) ◽  
pp. 51-55
Author(s):  
Aram Baram ◽  
Zirak Anwar Tayeb ◽  
Delan Ahmed Bakir

2014 ◽  
Vol 4 (2) ◽  
pp. 121
Author(s):  
AjaykumarR Gajengi ◽  
AnandkumarG Sharma ◽  
SunilM Mhaske ◽  
SujataK Patwardhan

2013 ◽  
Vol 71 (3) ◽  
pp. 338-340
Author(s):  
Tu-bing Xu ◽  
Wen-Yuan Liu ◽  
Geng Chen ◽  
Huai-zhi Wang ◽  
Ping Bie

2009 ◽  
Vol 50 (4) ◽  
pp. 975
Author(s):  
M.N. Tameo ◽  
K.D. Calligaro ◽  
M.J. Dougherty ◽  
L. Antin

2015 ◽  
Vol 100 (7-8) ◽  
pp. 1190-1193 ◽  
Author(s):  
Mohsen Ayati ◽  
Jafar Shahbazi ◽  
Ali Tehranchi ◽  
Elnaz Ayati ◽  
Yousef Rezaei

Adrenocortical carcinoma (ACC) is a rare aggressive tumor. Renal vein and inferior vena cava (IVC) thrombi have been found as uncommon presentations of ACC; however, the implementation of comprehensive therapy has remained controversial in such cases. We report a case of a 46-year-old woman with a large ACC associated with the invasion of tumor to IVC confirmed by imaging and immunohistochemistry examinations. The patient was treated successfully using aggressive surgery, including adrenalectomy and thrombectomy adjunct to an adrenocorticolytic agent. However, she died of metastasis complications at 3-month follow-up period. ACC is a rare malignancy, mostly presenting in advanced stages with poor prognosis. Implementing aggressive surgical therapy might be effective for the management of such cases; however, the short survival duration in our case underscores the need for defining the precise therapy of metastatic ACC associated with venous invasion.


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