metricas
covid
Buscar en
Cirugía Española (English Edition)
Toda la web
Inicio Cirugía Española (English Edition) Treatment of Caval Vein Thrombosis Associated With Renal Tumors
Información de la revista
Vol. 95. Núm. 3.
Páginas 152-159 (marzo 2017)
Visitas
7055
Vol. 95. Núm. 3.
Páginas 152-159 (marzo 2017)
Original article
Acceso a texto completo
Treatment of Caval Vein Thrombosis Associated With Renal Tumors
Tratamiento de la trombosis de vena cava inferior asociada a los tumores renales
Visitas
7055
Carlos Jiménez-Romeroa,
Autor para correspondencia
carlos.jimenez@inforboe.es

Corresponding author.
, María Condeb, Federico de la Rosac, Alejandro Manriquea, Jorge Calvoa, Óscar Casoa, Carlos Muñoza, Alberto Marcacuzcoa, Iago Justoa
a Unidad de Cirugía Hepato-Bilio-Pancreática y Trasplante de Órganos Abdominales, Hospital Universitario Doce de Octubre, Universidad Complutense de Madrid, Madrid, Spain
b Servicio de Cirugía General, Hospital Universitario Lucus Augusti, Lugo, Spain
c Servicio de Urología, Hospital Doce de Octubre, Madrid, Spain
Este artículo ha recibido
Información del artículo
Resumen
Texto completo
Bibliografía
Descargar PDF
Estadísticas
Figuras (4)
Mostrar másMostrar menos
Tablas (2)
Table 1. Classification of IVC Thrombosis Levels.
Table 2. Renal Tumors With Vena Cava Thrombosis.
Mostrar másMostrar menos
Abstract
Introduction

Renal carcinoma represents 3% of all solid tumors and is associated with renal or inferior caval vein (IVC) thrombosis between 2% and 10% of patients, extending to right atrial in 1% of cases.

Methods

This is a retrospective study that comprises 5 patients who underwent nephrectomy and thrombectomy by laparotomy because of renal tumor with IVC thrombosis level III.

Results

Four patients were males and one was female, and the mean age was 57.2 years (range: 32–72). Most important clinical findings were hematuria, weight loss, weakness, anorexia, and pulmonary embolism. Diagnostic confirmation was performed by CT scanner. Metastatic disease was diagnosed before surgery in 3 patients. Suprahepatic caval vein and hepatic hilium (Pringle's maneouver) were clamped in 4 patients, and ligation of infrarrenal caval vein was carry out in one patient.

Five patients developed mild complications (Clavien I/II). No patient died and the mean hospital stay was 8.6 days. All patients were treated with chemotherapy, and 3 died because distant metastasis, but 2 are alive, without recurrence, at 5 and 60 months, respectively.

Conclusions

Nephrectomy and thrombectomy in renal tumors with caval thrombosis can be curative in absence of metastasis or, at less, can increase survival or quality of live. Then these patients must be treated in liver transplant units because major surgical and anesthesiologic expertise. Adjuvant treatment with tyrosin kinase inhibitors must be validate in the future with wider experiences.

Keywords:
Renal tumor
Caval thrombosis
Caval vein
Tumoral thrombus
Resumen
Introducción

El carcinoma renal representa el 3% de los tumores sólidos y se asocia a trombosis de la vena renal o vena cava inferior (VCI) en el 2-10% de los pacientes; se extiende hasta la aurícula derecha en el 1% de los casos.

Métodos

Estudio retrospectivo de una serie de 5 enfermos intervenidos por tumor renal con trombosis tumoral de VCI de nivel iii, tratados con nefrectomía y trombectomía por laparotomía.

Resultados

Cuatro de los pacientes eran hombres y uno era mujer, con una edad media de 57,2 años (rango: 32-72). Como clínica predominó la hematuria, síndrome constitucional y tromboembolia pulmonar. La confirmación diagnóstica fue por TAC. En 3 pacientes se detectaron metástasis antes de la cirugía. Se realizó Pringle y pinzamiento de vena cava suprahepática en 4 pacientes y ligadura de VCI infrarrenal en uno.

Complicaciones leves (Clavien I/II) se presentaron en 5 pacientes. La mortalidad fue nula y la estancia hospitalaria media fue de 8,6 días. Todos los pacientes se trataron con quimioterapia; fallecieron 3 por metástasis a distancia, permanecen 2 vivos, sin recidiva, a los 5 y 60 meses. Supervivencia media: 26,6 meses.

Conclusiones

La nefrectomía y la trombectomía en tumores renales con trombosis de cava pueden ser curativas en ausencia de metástasis o, al menos, pueden aumentar la supervivencia y mejorar la calidad de vida. Para ello estos pacientes deberían tratarse en unidades de trasplante hepático por su mayor experiencia quirúrgica y anestésica. El tratamiento adyuvante con inhibidores de la tirosina cinasa debe validarse en el futuro con experiencias más amplias.

Palabras clave:
Tumor renal
Trombosis de cava
Vena cava
Trombo tumoral
Texto completo
Introduction

Renal cell carcinomas represent 3% of solid tumors.1 They cause a thrombus in the renal vein or inferior vena cava (IVC) in 2–10% of patients,2,3 and the thrombus extends to the right atrium in 1% of cases.2 The treatment indicated in these patients involves nephrectomy and thrombectomy of the cava, although this surgery also presents morbidity and mortality. In order to reduce these complications, it is necessary to identify and adequately expose the vena cava, liver and retroperitoneum in conjunction with the Urology Department in order to conduct the nephrectomy. Before surgery, is it essential to define the exact location of the thrombus in the cava to plan the best possible surgical approach. Depending on the location of the thrombus in the IVC, different techniques have been used, such as laparotomy,4–6 assisted laparoscopy,7 venovenous bypass8 or cardiopulmonary bypass with mild hypothermia.9 In this study, we present our experience in the treatment of three tumors by laparotomy.

Methods

We present a retrospective study of patients with renal tumor and thrombosis of the inferior vena cava that had been treated surgically between 2011 and 2016 by our HBP Surgery and Abdominal Organ Transplantation Units in collaboration with the Urology Department. The objective of this case series is to explain the symptoms, diagnosis and surgical techniques performed to locate the thrombus, as well as to analyze perioperative morbidity and mortality.

This series includes 5 patients, for whom demographic, preoperative, intraoperative and postoperative variables (Clavien et al. classification10), histological characteristics and survival were collected and analyzed. The classification adopted was the Ciancio et al. classification,11 which is based on the extension or invasion of the thrombus in the IVC (Table 1, Fig. 1). Out of the 5 cases, one corresponded with level IIIa, 3 IIIb and one IIIc. The radiological diagnosis was reached with ultrasound and CT in all cases, which demonstrated the level of invasion of the thrombus in the IVC (Fig. 2).

Table 1.

Classification of IVC Thrombosis Levels.

I Thrombus limited to the renal vein 
II Thrombus in infrahepatic IVC 
III Thrombus in retrohepatic IVC 
 
a) Thrombus in retrohepatic IVC, under the suprahepatic veins 
b) Thrombus in retrohepatic IVC in contact with the orifice of the suprahepatic veins 
c) Thrombus in the retrohepatic IVC, above the suprahepatic veins but under the diaphragm 
d) Thrombus in the suprahepatic and supradiaphragmatic IVC, reaching the intrapericardial IVC, although subatrial 
 
IV Thrombus in the right atrium 

Source: from Ciancio et al.11

Fig. 1.

Classification of thrombosis of the inferior vena cava (according to Ciancio et al.11).

(0.23MB).
Fig. 2.

Renal tumors with thrombosis of the inferior vena cava (cases 1, 2, 4 and 5) with levels IIIa, IIIb and IIIc, according to the Ciancio et al. classification.11

(0.4MB).

As for the surgical technique (except for level IIIa), in cases where the thrombus was proximal to the suprahepatic veins, intraoperative transesophageal echocardiogram was used to evaluate the mobility of the thrombus during surgery. We used an inverted T incision in 3 patients and a Mercedes in the remaining 2, which are standard incisions in liver transplantation. In all cases, we used a Stieber rib grip to widely separate the rib edge upwards, which allowed us to comfortably carry out the dissection of the liver and IVC. Renal tumors, especially large ones, present infiltration, firm adhesions and displacement of other organs (duodenum-pancreas, colon-hepatic angle and hepatic hilum in case 1, colon-hepatic angle in case 2 and tail of the pancreas in case 5). Initially, we freed the posterolateral side of the kidney using a posterior approach to identify, ligate and divide the renal artery, reducing collateral circulation and facilitating renal dissection.

Liver mobilization is performed similarly to liver transplantation: ligature and division of the round ligament; division with electrocoagulation of the falciform ligament, coronary and triangular ligaments, both on the right as well as the left, as well as the hepatorenal ligament. The liver pedicle is surrounded with a vascular loop for a possible Pringle maneuver. Dissection, ligation and division of the retrohepatic veins (piggy-back technique) are completed to expose the IVC and its entire extension, below the suprahepatic veins. The suprahepatic IVC is dissected and surrounded by a vascular loop for potential posterior clamping. This dissection provides for resolution of all cases of levels IIIa and IIIb IVC thrombosis, performing suprahepatic or infrahepatic clamping (below the suprahepatic veins) and clamping below the thrombus, usually at the infrarenal level. If the piggy-back is not complete (without dissection of retrohepatic veins of the caudate lobe), the suprahepatic IVC is clamped at levels IIIa and IIIb for 10–15min along, accompanied by a Pringle maneuver of equal duration. At level IIIc, we performed the same dissection, but “milked” the thrombus caudally before clamping the suprahepatic IVC.

Although we do not present any cases, at levels IIId (intrapericardial IVC thrombus) or IV (as long as the thrombus is not adhered to the atrium), the thrombus can be removed abdominally, as in previous levels, by infrahepatic cavotomy with previous diaphragmatic incision, intrapericardial dissection of the IVC, and milking the thrombus with the fingers until it surpasses the infrahepatic IVC, at which time it is clamped at this level above the thrombus.

Once this dissection is performed, we place the patient in Trendelenburg position, clamp the infrarenal IVC (below the thrombus) and the renal vein affected by the thrombus, the contralateral renal vein and the IVC above the thrombus of the cava (at the infrahepatic level, if we have performed a complete piggy-back, or at the suprahepatic level supplemented with a Pringle maneuver if it is incomplete). At this time, we perform a longitudinal cavotomy measuring 3–5cm and extract the thrombus with the index finger, washing afterwards with heparinized saline. A longitudinal continuous suture of the IVC is then carried out with 4-5/0 polypropylene. Before making the last stitch, we release the infrarenal IVC and the contralateral renal vein to eliminate thrombi and air, and then fill with blood the lumen of the IVC previously occupied by the thrombus. Simultaneously, the Pringle and IVC clamps are removed above the thrombus. The renal vein affected by the tumor thrombosis is divided at its union with the IVC, thereby impeding a residual tumor thrombus from remaining in the stump, and the nephrectomy is then completed (Figs. 3 and 4).

Fig. 3.

(A) Dissection of the suprahepatic vena cava; (B) piggy-back and dissection of the renal veins and infrarenal vena cava; (C) cavotomy and extraction of the thrombus; (D) cavography.

(0.25MB).
Fig. 4.

(A) Right renal tumor with thrombosis of the cava (IIIb); and (B) left renal tumor with thrombosis of the cava (IIIc).

(0.17MB).

In our case 4 with level IIIb thrombosis, a soft thrombus was also detected, which began 3cm below the renal veins and reached the iliac veins. In these cases, important chronic collateral circulation develops, in such a way that the gonadal vein and the lumbar branches connect with the azygos and hemiazygos system to reach the right atrium. Thus, after the aforementioned cava thrombectomy, we double-ligated the infrarenal IVC with silk 1-0 above the soft thrombus to prevent its migration toward the atrium. The mentioned collateral veins should not be ligated so as not to compromise the venous return toward the atrium. Proper anesthetic management of these patients is also very important by anesthesiologists with experience in liver transplantation.

Results

Out of this series of 5 patients, 4 were men and one was a woman, with a mean age of 57.2 years (range: 32–72). Predominant symptoms included hematuria, weight loss and pulmonary thromboembolism (PTE). In all cases, ultrasound was performed as the first diagnostic test, followed by CT scan for confirmation (PET/CT in one patient). In 3 patients, pulmonary, hepatic, bone or cerebral metastases were detected before surgery.

Clamping of the suprahepatic IVC and Pringle maneuver (10–15min) was performed in 4 patients, while in the first case (level IIIa) clamping was done under the suprahepatic veins. The infrarenal IVC was clamped (below the thrombus) in all cases for 10–15min. Definitive silk ligation of the infrarenal IVC above the soft thrombus, after thrombectomy of the main thrombus, was performed in one patient. Mean surgical time for nephrectomy and thrombectomy was 334min (range: 240–400), and mean transfusion of packed red blood cells was 6.4 units.

The primitive tumor was located in the right kidney in 4 cases and in the left in one, with a size of 5–20cm. In 4 patients, the tumor was comprised of club cells, while the other was a Ewing tumor. Tumor cells were isolated in the cava thrombus in all patients, whereas the adrenal gland showed no tumor invasion in any of the cases.

Postoperative complications were minor in all patients (Clavien I in 3 and Clavien II in 2), with an average hospital stay of 8.6 days. Out of the 5 patients, 4 were treated with chemotherapy (one currently in treatment), and radiotherapy was added to the patient with renal Ewing's sarcoma. Two patients survived to 60 months, and the last patient treated to 5 months; the remaining 3 died of metastatic disease at 11, 18 and 39 months, with a mean survival of 26.6 months (Table 2).

Table 2.

Renal Tumors With Vena Cava Thrombosis.

 
Sex  Male  Female  Male  Male  Male 
Age (yrs)  32  69  69  44  72 
Symptoms  Varicocele, hematuria  Constitutional synd., hematuria  Constitutional synd., hematuria, PTE, edemas of lower limbs  Constitutional synd., pain, PTE  Asymptomatic 
Preoperative
ASA classification  III  III  III  III 
Imaging studies  Ultrasound+CT  Ultrasound+CT  Ultrasound+PET-CT  Ultrasound+CT  Ultrasound+CT 
Preoperative TNM  T3bN0M0  T3bN0M1  T3bN0M1  T3bN0M1  T3bN0M0 
Hb (g/dL)  13.8  8.4  14.1  11  11.7 
Platelets  305000  256000  310000  306000  377000 
Intraoperative
Laparotomic incision  Mercedes  Mercedes  Inverted T  Inverted T  Inverted T 
Type of thrombus (classif.)  IIIa  IIIb  IIIb  IIIb  IIIc 
Suprahepatic IVC clamping  No  Yes  Yes  Yes  Yes 
Pringle clamping (min)  No  10  12  15  10 
Infrarenal IVC clamping (min)  11  10  12  15  10 
Length of cavotomy (cm) 
Ligature/infrarenal cava division  No  No  No  Yes  No 
Nephrectomy  Right  Right  Right  Right  Left 
Surgical time (min)  240  340  330  400  360 
Transfusion (erythrocytes) 
Transfusion FFP (U)  No 
Vasoactive agents  No  Yes  No  Yes  Yes 
Postoperative
Complications (Clavien)  II  II 
Hospital stay (days)  15 
Renal tumor
Size (cm)  20  10  7.5 
TNM classification:  pT4NxMx  pT3bN0Mx  pT3bN0Mx  pT3bN0Mx  pT3bN0Mx 
Histological type  PNET (Ewing)  Club cells  Club cells  Club cells  Club cells 
Fuhrman classification 
Tumor cells in thrombus  Yes  Yes  Yes  Yes  Yes 
Tumor cells in adrenal gland  No  No  No  No  No 
Follow-up
Adjuvant treatment  VAC/CHOP+IFO/VP16
RTx (4500Gy) 
Sunitinib (50mg/day) (1month)  Sunitinib (50mg/day)  Pazopanib (800mg/day)  Axitinib 
Cause of death  No  Metastases in lung, brain  Metastases in lung, bones, liver  Metastases in lung, bones, liver  No 
Survival (months)  60 (disease-free)  39  11  18 
Current status  Living  Deceased  Deceased  Deceased  Living 

FFP: fresh frozen plasma; RTx: radiotherapy; PTE: pulmonary thromboembolism; PNET: primitive neuroectodermal tumor; TNM: tumor node metastasis; IVC: inferior vena cava.

Discussion

In the Memorial series,3 82% of patients with renal tumor and IVC thrombosis were symptomatic at the time of diagnosis, and 19% had distant metastases. On the other hand, in the Mayo Clinic series,12 about 40% of these patients with renal tumor and IVC thrombosis presented metastases at the time of surgery: 28.5% at a distance and 11.7% of the regional lymph nodes.

In our short series, taking into account that all patients presented level III thrombosis, 80% showed symptoms (mainly constitutional syndrome, hematuria and PTE), and 60% had distant metastases at the time of diagnosis.

The diagnosis of an IVC thrombus is confirmed with magnetic resonance imaging, which is especially useful for detecting a soft thrombus in the infrarenal IVC,13 or by multi-slice CT scan.14

Level I or II IVC thrombi are treated by dissection of the IVC, without the need for a complete piggy-back, with clamping of the contralateral renal vein and the IVC above and below the thrombus, followed by cavotomy and thrombectomy.

It has been demonstrated that, in cases of level III IVC thrombi, thrombectomy can be performed without using bypass techniques, thereby basically avoiding neurological, pulmonary, or coagulopathy complications.3,4,10 In level IV thrombosis, venovenous or cardiopulmonary bypass can be avoided if the thrombus is free (not adhered to the atrium) using the intraabdominal approach, followed by division of the diaphragm. Thus, the intrapericardial IVC and right atrium are controlled, and the thrombus is “milked” with the fingers toward the IVC below the suprahepatic veins.15

If ligation and division of all retrohepatic veins or the piggy-back technique are used as in liver transplantation, it is not necessary to clamp the hepatic hilum in level III thrombosis prior to thrombectomy.15 Alternatively, in our experience, in levels I, II and III it is not necessary for the piggy-back to be complete if we clamp the hepatic hilum (Pringle maneuver) and the suprahepatic IVC for 10–15min, which is sufficient time to perform the 3–5cm cavotomy, thrombectomy and suture of the vena cava.

In the rarest case of thrombosis with complete IVC obstruction associated with an infrarenal soft thrombus reaching up to the iliac veins, collateral circulation formed through the lumbar veins that drain the system of the azygos and hemiazygos veins. Here, thrombectomy of the formed thrombus should be done with ligation or division with a stapler of the IVC above the soft thrombus, which is left intact to prevent its mobilization toward the atrium.16

It has been observed that the higher the level of the thrombus, the greater the need for blood transfusion during surgery.3,15 Two American series report between 4.3 and 4.7 units of transfused packed red blood cells,3,15 while the mean number of units transfused in our patients was 5.4. The reported average surgical time has been between 250 and 467min,3,12,15 while the mean was 334min in our patients.

In our series, we have observed the presence of tumor cells in all the cava thrombi but the absence of these cells in the adrenal gland excised together with the renal tumor.

In the series of 77 patients at Memorial,3 which considered all levels of thrombosis, the incidence of major complications was 36% and minor complications 18%. Hemorrhage and PTE are serious complications associated with the higher level of cranial extension of the thrombus.17 Our patients have only presented minor complications (Clavien I or II). According to different series,3,6,12 perioperative mortality was 3.5–6%, which was null in our experience. Mean reported hospital stay was between 7 and 9 days12,15 and 8.6 days in our series.

The higher the level of the thrombus, the more advanced the tumor stage,3,15 and median survival decreases.18,19 Independent factors of poor prognosis include the presence of metastasis at the time of diagnosis and non-club cell renal tumors.6 There is controversy regarding radical surgery in cases of renal tumors with distant metastases and cava thrombosis: some authors state that the possibility of increased survival is not justified by the high morbidity and mortality associated with surgery.20 However, recently, other authors have demonstrated the absence of differences in morbidity and mortality rates, whether or not there is distant metastasis.21

After surgery, 5-year survival is 15–20% with regional or distant metastases and only 4% with both types of metastases. In cases with no metastasis, survival reaches 60%.12 However, even in patients with distant metastases, surgery is still indicated as it increases survival and improves quality of life.15,22–24 In patients with distant metastases, mean survival rates of 13 months and 2-year survivals of 26% have been reported.25 In general, nephrectomy and thrombectomy are associated with greater survival than conservative treatment in cases of renal tumors with IVC thrombosis (19.8 months versus 6.9 months).18 Another series confirms that the mean survival of patients who are not treated surgically is only 5 months.26 Surgical treatment of metastatic lesions can be performed simultaneously with the renal surgery or at a later stage, depending on the patient's condition. Thus, surgical rescue of a metachronous lesion is considered when it is a single lesion in a patient in good general condition.27

Recently, several series have reported patients treated by laparoscopy28 or robotic surgery,29,30 with results similar to those obtained by laparotomy.

Several cases of neoadjuvant therapy with sunitinib have been reported, in which level IV thrombi have been reduced in size.31 Initial treatment with tyrosine-kinase inhibitors (sunitinib, pazopanib, axitinib) should be considered for its potential in both infra-staging as well as the reduction of postoperative morbidity.32

We conclude that nephrectomy and thrombectomy in renal tumors with cava thrombosis may be a curative technique in the absence of metastasis or may at least increase survival and improve quality of life. These patients should be treated in liver transplantation units due to their greater surgical and anesthetic experience. In the future, adjuvant treatment with tyrosine-kinase inhibitors should be validated with more extensive studies.

Authorship/Collaborators

- Carlos Jiménez-Romero: study design; composition of the article.

- María Conde: data collection; composition of the article.

- Federico de la Rosa: data collection; analysis and interpretation of the results.

- Alejandro Manrique: analysis and interpretation of the results; critical review and approval of the final version.

- Jorge Calvo: data collection; analysis and interpretation of the results.

- Óscar Caso: data collection; analysis and interpretation of the results.

- Carlos Muñoz: data collection; analysis and interpretation of the results.

- Alberto Marcacuzco: data collection; critical review and approval of the final version.

- Iago Justo: critical review and approval of the final version; study design.

Conflict of Interests

The authors have no conflict of interests to declare.

References
[1]
A. Jemal, R. Siegel, J. Xu, E. Ward.
Cancer statistics 2010.
CA Cancer J Clin, 60 (2010), pp. 277-300
[2]
V.F. Marshall, R.G. Middleton, G.R. Holswade, E.I. Goldsmith.
Surgery for renal cell carcinoma in the vena cava.
J Urol, 103 (1970), pp. 414-420
[3]
M.G. Kaag, C. Toyen, P. Russo, A. Cronin, R.H. Thompson, J. Schiff, et al.
Radical nephrectomy with vena caval thrombectomy: a contemporary experience.
BJU Int, 107 (2010), pp. 1386-1393
[4]
M.L. Blute, B.C. Leibovich, C.M. Lohse, J.C. Cheville, H. Zincke.
The Mayo Clinic experience with surgical management complications and outcome for patients with renal cell carcinoma and venous tumour thrombus.
[5]
D.P. Parekh, M.S. Cookson, W. Chapman, F. Harrell, N. Wells, S.S. Chang.
Renal cell carcinoma with renal vein and inferior vena caval involvement: clinicopathological features surgical techniques and outcomes.
[6]
G. Ciancio, M. Manoharan, D. Katkoori, R. de los Santos, M.S. Soloway.
Long-term survival in patients undergoing radical nephrectomy and inferior vena cava thrombosis: single center experience.
Eur Urol, 57 (2010), pp. 667-672
[7]
A. Henderson, D. Murphy, K. Jaganathan, W.W. Roberts, J.S. Wolf Jr., A. Rané, et al.
Hand-assisted laparoscopic nephrectomy for renal cell cancer with renal vein tumor thrombus.
[8]
C.F. Granberg, S.A. Boorjian, H.V. Schaff, OrszulakTA, B.C. Leibovich, C.M. Lohse, et al.
Surgical management complications and outcome of radical nephrectomy with inferior vena cava tumor thrombectomy facilitated by vascular bypass.
[9]
U.K. Chowdhury, A.K. Mishra, A. Seth, P.N. Dogra, J.H.V. Honnakere, G.K. Subramaniam, et al.
Novel techniques for tumor thrombectomy for renal cell carcinoma with intraatrial tumor thrombus.
Ann Thorac Surg, 83 (2007), pp. 1731-1736
[10]
P. Clavien, J. Sanabria, S. Strasberg.
Proposed classification of complications of surgery with examples of utility in cholecystectomy.
Surgery, 111 (1992), pp. 518-526
[11]
G. Ciancio, A. Vaidya, M. Savoie, M. Soloway.
Management of renal cell carcinoma with level III thrombus in the inferior vena cava.
[12]
S. Boorjian, S. Sengupta, M. Blute.
Renal cell carcinoma: vena caval involvement.
[13]
A. Oto, B.R. Herts, E.M. Remer, A.C. Novick.
Inferior vena cava tumor thrombus in renal cell carcinoma: staging by MR imaging and impact on surgical treatment.
Am J Roentgenol, 171 (1998), pp. 1619-1624
[14]
T.J. Guzzo, P.M. Pierorazio, E.M. Schaeffer, E.K. Fishman, M.E. Allaf.
The accuracy of multidetector computerized tomography for evaluating tumor thrombus in patients with renal cell carcinoma.
J Urol, 181 (2009), pp. 486-491
[15]
G. Ciancio, M.S. Soloway.
Renal cell carcinoma with tumor thrombus extending above diaphragm: avoiding cardiopulmonary bypass.
[16]
M.L. Blute, S.A. Boorjian, B.C. Leibovich, C.M. Lohse, I. Frank, J. Karnes.
Results of inferior vena cava interruption by Greenfield filter ligation or resection during radical nephrectomy and tumor thrombectomy.
J Urol, 178 (2007), pp. 440-445
[17]
T.W. Kown, H. Kim, K.M. Moon, Y.P. Cho, C. Song, C.S. Kim, et al.
Surgical treatment of inferior vena cava tumor thrombus in patients with renal cell carcinoma.
J Korean Med Sci, 25 (2010), pp. 104-109
[18]
A. Haferkamp, P.J. Bastian, H. Jakobi, M. Pritsch, J. Pfitzenmaier, P. Albers, et al.
Renal cell carcinoma with tumor thrombus extension into the vena cava: prospective long-term follow-up.
J Urol, 177 (2007), pp. 1703-1708
[19]
S. Klaver, S. Joniau, R. Suy, R. Oyen, H. van Poppel.
Analysis of renal cell carcinoma with subdiaphragmatic macroscopic venous invasion (T3b).
[20]
D.J. Swierzewski, M.J. Swierzewski, J.A. Libertino.
Radical nephrectomy in patients with renal cell carcinoma with venous vena caval and auricular extension.
Am J Surg, 168 (1994), pp. 205-209
[21]
E.H. Lambert, P.M. Pierorazio, A. Shabsigh, C.A. Olsson, M.C. Benson, J.M. McKiernan.
Prognostic risk stratification and clinical outcomes in patients undergoing surgical treatment for renal cell carcinoma with vascular tumor thrombus.
Urology, 69 (2007), pp. 1054-1058
[22]
E. Bromwich, D. Hendry, M. Aitchinson.
Cytoreductive nephrectomy: is a realistic option in patients with renal cancer?.
BJU Int, 89 (2002), pp. 523-525
[23]
M.A. Goetzl, E.T. Goluboff, A.M. Murphy, A.E. Katz, M. Mansukhani, I.S. Sawczuk, et al.
A contemporary evaluation of cytoreductive nephrectomy with tumor thrombus: morbidity and long-term survival.
Urol Oncol, 22 (2004), pp. 182-187
[24]
Z. Kirkali, H. van Poppel.
A critical analysis of surgery for kidney cancer with vena cava invasion.
Eur Urol, 52 (2007), pp. 658-662
[25]
G. Staehler, D. Brkovic.
The role of radical surgery for renal cell carcinoma with extension into the vena cava.
J Urol, 163 (2000), pp. 1671-1675
[26]
A.C. Reese, J.M. Whitson, M.V. Meng.
Natural history of untreated renal cell carcinoma with venous tumor thrombus.
Urol Oncol, 31 (2013), pp. 1305-1309
[27]
B. Ljungberg, K. Bensalah, S. Canfield, S. Dabestani, Hofman, M. Hora, et al.
EAU guidelines on renal cell carcinoma: 2014 update.
Eur Urol, 67 (2015), pp. 913-924
[28]
K. Lue, C.M. Russell, J. Fisher, T. Kurian, G. Agarwal, A. Luchey, et al.
Predictors of postoperative complications in patients who undergo radical nephrectomy and IVC thrombectomy: a large contemporary tertiary center analysis.
Clin Genitourin Cancer, 14 (2016), pp. 89-95
[29]
Shao, J. Li, C. Qin, Q. Lv, X. Ju, P. Li, et al.
Laparoscopic radical nephrectomy and inferior vena cava thrombectomy in the treatment of renal cell carcinoma.
Eur Urol, 68 (2016), pp. 115-122
[30]
I.S. Gill, C. Metcalfe, A. Abreu, V. Duddalwar, S. Chopra, M. Cunningham, et al.
Robotic level III vena cava tumor thrombectomy: initial series.
J Urol, 194 (2015), pp. 929-938
[31]
P.I. Karakiewicz, N. Suardi, C. Jeldres, P. Audet, P. Ghosn, J.J. Patard, et al.
Neoadjuvant sutent induction therapy may effectively down-stage renal cell carcinoma atrial thrombi.
Eur Urol, 53 (2008), pp. 845-848
[32]
G. Di Lorenzo, R. Autorino, C.N. Sternberg.
Metastatic renal cell carcinoma: recent advances in the targeted therapy era.
Eur Urol, 56 (2009), pp. 959-971

Please cite this article as: Jiménez-Romero C, Conde M, de la Rosa F, Manrique A, Calvo J, Caso Ó, et al. Tratamiento de la trombosis de vena cava inferior asociada a los tumores renales. Cir Esp. 2017;95:152–159.

Copyright © 2017. AEC
Descargar PDF
Opciones de artículo
es en pt

¿Es usted profesional sanitario apto para prescribir o dispensar medicamentos?

Are you a health professional able to prescribe or dispense drugs?

Você é um profissional de saúde habilitado a prescrever ou dispensar medicamentos