Hereditary renal cell carcinoma: results and place of conventional conservative surgery

被引:0
作者
Roupret, M
Hupertan, V
Chretien, Y
Mejean, A
Richard, S
Chauveau, D
Dufour, B
机构
[1] Hop Necker Enfants Malad, Serv Urol, Paris, France
[2] Hop Necker Enfants Malad, Serv Nephrol, Paris, France
[3] SPSS France, Paris, France
来源
PROGRES EN UROLOGIE | 2003年 / 13卷 / 06期
关键词
heredity; renal cell carcinoma; partial nephrectomy;
D O I
暂无
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Objectives: To report the results of conservative surgery for the treatment of hereditary renal cell carcinoma (RCC) and to define its place with respect to new less invasive treatment options. Material and Method: Over a period of 14 years, 30 women and 26 men were operated for one or several hereditary RCC either by radical nephrectomy or nephron-sparing excision, via a lumbar or subcostal incision, when the diameter of at least one RCC was greater than 2.5 cm. Results: 92 operations were performed: 62 local excisions and 30 nephrectomies. The TNM stage was: 75 pT1, 14 pT2, 3 pT3b; 4 N+; 3 M+. 26 patients (46%) were operated at least twice. Two or more RCC were resected in 43 cases (47%). In the case of nephron-sparing surgery, mean blood loss was 175 +/- 231.7 cc (range: 50-1300 cc); mean pedicle clamping time (97% of cases) was 32 +/- 10.4 min (range: 10-50 min); mean preoperative serum creatinine was 85 +/- 18 mumol/L (range: 52-150 mumol/L) and mean postoperative serum creatinine was 105 +/- 80 mumol/L (range: 59-576 mumol/L); the calculated tumour recurrence rate was 24% at 5 years and 80% at 8 years; overall 5-year survival was 100% and overall 10-year survival was 67%. The median follow-up was 55.9 months. Conclusion: When hereditary RCCs are situated between 2.5 cm and 6 cm in diameter, nephron-sparing surgery is the reference treatment. Modern imaging and genetic screening should allow early detection of increasingly smaller RCCs. In the future, less invasive treatment options could replace surveillance for RCCs less than 2 cm and eventually reduce the indications for local excision.
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收藏
页码:1295 / 1299
页数:5
相关论文
共 20 条
  • [1] Hereditary renal cancers
    Choyke, PL
    Glenn, GM
    Walther, MM
    Zbar, B
    Linehan, WM
    [J]. RADIOLOGY, 2003, 226 (01) : 33 - 46
  • [2] Chretien Y, 1997, Prog Urol, V7, P939
  • [3] Renal cell carcinoma in the solitary kidney: An analysis of complications and outcome after nephron sparing surgery
    Ghavamian, R
    Cheville, JC
    Lohse, CM
    Weaver, AL
    Zincke, H
    Blute, ML
    [J]. JOURNAL OF UROLOGY, 2002, 168 (02) : 454 - 459
  • [4] Comparative analysis of laparoscopic versus open partial nephrectomy for renal tumors in 200 patients
    Gill, IS
    Matin, SF
    Desai, MM
    Kaouk, JH
    Steinberg, A
    Mascha, E
    Thornton, J
    Sherief, MH
    Strzempkowski, B
    Novick, AC
    [J]. JOURNAL OF UROLOGY, 2003, 170 (01) : 64 - 68
  • [5] Goldfarb DA, 1998, J INTERN MED, V243, P563
  • [6] Laparoscopic partial nephrectomy for renal tumor:: Single center experience comparing clamping and no clamping techniques of the renal vasculature
    Guillonneau, B
    Bermúdez, H
    Gholami, S
    El Fettouh, H
    Gupta, R
    Rosa, JA
    Baumert, H
    Cathelineau, X
    Fromont, G
    Vallancien, G
    [J]. JOURNAL OF UROLOGY, 2003, 169 (02) : 483 - 486
  • [7] Parenchymal sparing surgery in patients with hereditary renal cell carcinoma: 10-year experience
    Herring, JC
    Enquist, EG
    Chernoff, A
    Linehan, WM
    Choyke, PL
    Walther, MM
    [J]. JOURNAL OF UROLOGY, 2001, 165 (03) : 777 - 781
  • [8] Von Hippel-Lindau disease: strategies in early detection (renal-, adrenal-, pancreatic masses)
    Hes, FJ
    Feldberg, MAM
    [J]. EUROPEAN RADIOLOGY, 1999, 9 (04) : 598 - 610
  • [9] Prevalence, morphology and biology of renal cell carcinoma in von Hippel-Lindau disease compared to sporadic renal cell carcinoma
    Neumann, HPH
    Bender, BU
    Berger, DP
    Laubenberger, J
    Schultze-Seemann, W
    Wetterauer, U
    Ferstl, FJ
    Herbst, EW
    Schwarzkopf, G
    Hes, FJ
    Lips, CJM
    Lamiell, JM
    Masek, O
    Riegler, P
    Mueller, B
    Glavac, D
    Brauch, H
    [J]. JOURNAL OF UROLOGY, 1998, 160 (04) : 1248 - 1254
  • [10] Prevalence of microscopic tumors in normal appearing renal parenchyma of patients with hereditary papillary renal cancer
    Ornstein, DK
    Lubensky, IA
    Venzon, D
    Zbar, B
    Linehan, WM
    Walther, MM
    [J]. JOURNAL OF UROLOGY, 2000, 163 (02) : 431 - 433