Renal lesions in von Hippel-Lindau disease:: The benign, the malignant, the unknown

被引:4
作者
Salomé, F
Colombeau, P
Fermeaux, V
Cazaux, P
Dumas, JP
Pfeifer, P
Moreau, JJ
Richard, S
Labrousse, F
机构
[1] CHU Dupuytren, Serv Urol, Dept Urol, F-87042 Limoges, France
[2] CHU Dupuytren, Dept Pathol, F-87042 Limoges, France
[3] CHU Dupuytren, Dept Radiol, F-87042 Limoges, France
[4] CHU Dupuytren, Dept Neurosurg, F-87042 Limoges, France
[5] Hop Necker Enfants Malad, Dept Nephrol, EPHE, Lab Neurooncol, Paris, France
关键词
angiomatosis; von Hippel-Lindau disease; renal cell carcinoma; renal cyst; surgery;
D O I
10.1159/000019771
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 describe the features and treatment of renal lesions in von Hippel-Lindau disease (VHL) from a series of patients, to highlight important issues in the management of these lesions. Materials and Methods: We performed a retrospective study in 7 patients with VHL who underwent surgery for renal lesions between January 1990 and July 1996. The initial evaluation consisted of an abdominal CT scan and renal arteriography. Results: The mean age of patients at the time of discovery was 38 (+/- 12.01 years). AU cases were of type 1. Radiology assessment underestimated the gravity of the lesions in 5 patients. In all patients, unilateral surgery was performed with the kidney being conserved in 4 cases. Of the 44 lesions removed, 23 had signs of progressiveness (atypical or malignant cyst, renal cell carcinoma), most of the cancers were of low grade. 84% of the lesions did not exceed 3 cm and 48% were less than or equal to 1 cm. During follow-up (42 months), 2 patients relapsed. Conclusion: The clinical and pathological features of renal lesions in VHL require strict and early follow-up (from the age of 15). Only under these circumstances should primary conservative surgery be performed, however, recurrences are frequent. This conservative approach remains to be validated by multicentric prospective studies.
引用
收藏
页码:383 / 392
页数:10
相关论文
共 35 条
[21]   CLINICAL-FEATURES AND NATURAL-HISTORY OF VONHIPPEL-LINDAU DISEASE [J].
MAHER, ER ;
YATES, JRW ;
HARRIES, R ;
BENJAMIN, C ;
HARRIS, R ;
MOORE, AT ;
FERGUSONSMITH, MA .
QUARTERLY JOURNAL OF MEDICINE, 1990, 77 (283) :1151-1163
[22]   Endolymphatic sac tumors - A source of morbid hearing loss in von Hippel-Lindau disease [J].
Manski, TJ ;
Heffner, DK ;
Glenn, GM ;
Patronas, NJ ;
Pikus, AT ;
Katz, D ;
Lebovics, R ;
Sledjeski, K ;
Choyke, PL ;
Zbar, B ;
Linehan, WM ;
Oldfield, EH .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1997, 277 (18) :1461-1466
[23]   VONHIPPEL-LINDAU DISEASE - INADEQUACY OF ANGIOGRAPHY FOR IDENTIFICATION OF RENAL CANCERS [J].
MILLER, DL ;
CHOYKE, PL ;
WALTHER, MM ;
DOPPMAN, JL ;
KRAGEL, PJ ;
WEISS, GH ;
LINEHAN, WM .
RADIOLOGY, 1991, 179 (03) :833-836
[24]   THE CLINICAL AND PATHOLOGICAL MANIFESTATIONS OF RENAL TUMORS IN VON HIPPEL-LINDAU DISEASE [J].
NELSON, JB ;
OYASU, R ;
DALTON, DP .
JOURNAL OF UROLOGY, 1994, 152 (06) :2221-2226
[25]   CLUSTERING OF FEATURES OF VONHIPPEL-LINDAU SYNDROME - EVIDENCE FOR A COMPLEX GENETIC-LOCUS [J].
NEUMANN, HPH ;
WIESTLER, OD .
LANCET, 1991, 337 (8749) :1052-1054
[26]   A PLEA FOR CONSERVATION OF KIDNEY IN RENAL ADENOCARCINOMA ASSOCIATED WITH VON HIPPEL-LINDAU DISEASE [J].
PEARSON, JC ;
WEISS, J ;
TANAGHO, EA .
JOURNAL OF UROLOGY, 1980, 124 (06) :910-912
[27]  
PETERSON GJ, 1977, ARCH SURG-CHICAGO, V112, P841
[28]   CHARACTERIZATION OF THE RENAL PATHOLOGY OF A FAMILIAL FORM OF RENAL-CELL CARCINOMA-ASSOCIATED WITH VON HIPPEL-LINDAU DISEASE - CLINICAL AND MOLECULAR-GENETIC IMPLICATIONS [J].
POSTON, CD ;
JAFFE, GS ;
LUBENSKY, IA ;
SOLOMON, D ;
ZBAR, B ;
LINEHAN, WM ;
WALTHER, MM .
JOURNAL OF UROLOGY, 1995, 153 (01) :22-26
[29]  
Richard S, 1994, Adv Nephrol Necker Hosp, V23, P1
[30]   VON HIPPEL-LINDAU DISEASE [J].
RICHARD, S ;
OLSCHWANG, S ;
CHAUVEAU, D ;
RESCHE, F .
M S-MEDECINE SCIENCES, 1995, 11 (01) :43-51