ROUTINE TOTAL BILATERAL ADRENALECTOMY IS NOT WARRANTED IN CHILDHOOD FAMILIAL PHEOCHROMOCYTOMA

被引:43
作者
ALBANESE, CT [1 ]
WIENER, ES [1 ]
机构
[1] UNIV PITTSBURGH,CHILDRENS HOSP PITTSBURGH,SCH MED,DEPT PEDIAT SURG,PITTSBURGH,PA 15260
关键词
PHEOCHROMOCYTOMA; CHILDHOOD; FAMILIAL; MULTIPLE ENDOCRINE NEOPLASIA SYNDROME;
D O I
10.1016/S0022-3468(05)80307-0
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
The surgical management of familial childhood pheochromocytoma is based on data derived from clinical series that have focused primarily on the multiple endocrine neoplasia (MEN)-associated cases. Prophylactic bilateral total adrenalectomy has been advocated for this group due to a high incidence of bilateral adrenal involvement and the propensity for tumor recurrence after partial adrenal resections. We retrospectively reviewed our experience with a cohort of children with nonsyndromatic familial pheochromocytoma to see if their surgical management should parallel that advocated for patients with the MEN syndrome. From 1977 through 1991, 17 children from 9 families with a strong family history of pheochromocytoma were treated at the Children's Hospital of Pittsburgh. None of the patients or their families displayed an association with the MEN syndrome. There were 13 males and 4 females with a mean age of 10.1 years. Follow-up was obtained on all patients and averaged 6 years. All tumors were located within the abdominal cavity. Seven patients presented with unilateral adrenal tumors while four patients had synchronous bilateral tumors. Eight patients had tumors in extraadrenal locations; 2 with concomittant adrenal tumors. Ten patients underwent total unilateral adrenalectomy with or without resection of extraadrenal tumor(s). All patients with synchronous bilateral adrenal tumors underwent unilateral adrenalectomy in combination with a partial contralateral adrenal resection without a recurrence after an average of 7.3 years. Three patients developed metachronous adrenal tumors an average of 4.2 years after their initial surgery. All required complete removal of the affected adrenal, resulting in two patients with bilateral adrenalectomies. All patients were normotensive without medication at the time of follow-up. In total, 82% of patients were cured by the initial surgical procedure, and only two required total bilateral adrenalectomy. © 1993 W.B. Saunders Company. All rights reserved.
引用
收藏
页码:1248 / 1252
页数:5
相关论文
共 13 条
  • [1] SURGICAL MANAGEMENT OF PHEOCHROMOCYTOMA IN CHILDREN
    BLOOM, DA
    FONKALSRUD, EW
    [J]. JOURNAL OF PEDIATRIC SURGERY, 1974, 9 (02) : 179 - 184
  • [2] CARNEY JA, 1975, MAYO CLIN PROC, V50, P3
  • [3] CARNEY JA, 1976, AM J CLIN PATHOL, V66, P279
  • [4] CATY MG, 1990, ARCH SURG-CHICAGO, V125, P978
  • [5] HUMAN ADRENAL GLAND WITH SPECIAL REFERENCE TO VASCULATURE
    DOBBIE, JW
    SYMINGTON, T
    [J]. JOURNAL OF ENDOCRINOLOGY, 1966, 34 (04) : 479 - +
  • [6] PHEOCHROMOCYTOMA IN THE PEDIATRIC AGE GROUP - CURRENT STATUS
    KAUFMAN, BH
    TELANDER, RL
    VANHEERDEN, JA
    ZIMMERMAN, D
    SHEPS, SG
    DAWSON, B
    [J]. JOURNAL OF PEDIATRIC SURGERY, 1983, 18 (06) : 879 - 884
  • [7] ASSOCIATION OF PHEOCHROMOCYTOMA WITH CARCINOMA OF THYROID GLAND
    SIPPLE, JH
    [J]. AMERICAN JOURNAL OF MEDICINE, 1961, 31 (01) : 163 - &
  • [8] MULTIPLE ENDOCRINE NEOPLASIA TYPE-2
    SIZEMORE, GW
    HEATH, H
    CARNEY, JA
    [J]. CLINICS IN ENDOCRINOLOGY AND METABOLISM, 1980, 9 (02): : 299 - 315
  • [9] PHEOCHROMOCYTOMA IN CHILDREN - REPORT OF 9 CASES AND REVIEW OF FIRST 100 PUBLISHED CASES WITH FOLLOW-UP STUDIES
    STACKPOLE, RH
    MELICOW, MM
    USON, AC
    [J]. JOURNAL OF PEDIATRICS, 1963, 63 (02) : 315 - +
  • [10] PHEOCHROMOCYTOMA IN CHILDREN - AN UPDATE
    STRINGEL, G
    EIN, SH
    CREIGHTON, R
    DANEMAN, D
    HOWARD, N
    FILLER, RM
    [J]. JOURNAL OF PEDIATRIC SURGERY, 1980, 15 (04) : 496 - 500