A case of neurofibromatosis type 1 with an aldosterone-producing adenoma of the adrenal

被引:6
作者
Biagi, P
Alessandri, M
Campanella, G
Castro, R
Totteri, A
Fanciullacci, M
机构
[1] Univ Florence, Dipartimento Med Interna, I-50139 Florence, Italy
[2] Abbadia San Salvatore Hosp, Dept Internal Med, Abbadia San Salvatore, SI, Italy
[3] Misericordia Hosp, Dept Internal Med, Grosseto, Italy
[4] Abbadia San Salvatore Hosp, Unit Cardiol, Abbadia San Salvatore, SI, Italy
关键词
Conn's syndrome; hypertension; neurofibromatosis type 1; tumour predisposition;
D O I
10.1046/j.1365-2796.1999.00577.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Neurofibromatosis type 1 is a phacomatosis, Neurofibromas are the most common tumours associated with the disease, and along with other tumours, make neurofibromatosis type 1 the most common tumour predisposing syndrome in humans. Hypertension may be coincidental, but at least two specific neurofibromatosis related causes must be considered, namely neurofibromatous involvement of the renal artery and pheochromocytoma. We have described the first known case of a patient with neurofibromatosis type 1 who developed hypertension due to an aldosterone-producing adenoma of the adrenal. The question of whether this association was coincidental or due to the tumour predisposition of neurofibromatosis type 1 was debated.
引用
收藏
页码:509 / 512
页数:4
相关论文
共 22 条
  • [1] Growth rate characteristics of acoustic neuromas associated with neurofibromatosis type 2
    Abaza, MM
    Makariou, E
    Armstrong, M
    Lalwani, AK
    [J]. LARYNGOSCOPE, 1996, 106 (06) : 694 - 699
  • [2] ABERRANT REGULATION OF RAS PROTEINS IN MALIGNANT-TUMOR CELLS FROM TYPE-1 NEUROFIBROMATOSIS PATIENTS
    BASU, TN
    GUTMANN, DH
    FLETCHER, JA
    GLOVER, TW
    COLLINS, FS
    DOWNWARD, J
    [J]. NATURE, 1992, 356 (6371) : 713 - 715
  • [3] NEUROFIBROMATOSIS - DISTRIBUTION OF LESIONS AND SURGICAL-TREATMENT
    BROMLEY, GS
    SHERMAN, JE
    GOULIAN, D
    [J]. ANNALS OF PLASTIC SURGERY, 1982, 8 (04) : 272 - 276
  • [4] A MAJOR SEGMENT OF THE NEUROFIBROMATOSIS TYPE-1 GENE - CDNA SEQUENCE, GENOMIC STRUCTURE, AND POINT MUTATIONS
    CAWTHON, RM
    WEISS, R
    XU, GF
    VISKOCHIL, D
    CULVER, M
    STEVENS, J
    ROBERTSON, M
    DUNN, D
    GESTELAND, R
    OCONNELL, P
    WHITE, R
    [J]. CELL, 1990, 62 (01) : 193 - 201
  • [5] CONN JW, 1955, J LAB CLIN MED, V45, P3
  • [6] Acute presentation of a neurogenic sarcoma in a patient with neurofibromatosis type 1: A pathological and molecular explanation
    Feldkamp, MM
    Lau, N
    Provias, JP
    Gutmann, DH
    Guha, A
    [J]. JOURNAL OF NEUROSURGERY, 1996, 84 (05) : 867 - 873
  • [7] GRAD E, 1972, J PEDIATR-US, V80, P804
  • [8] Guha A, 1996, ONCOGENE, V12, P507
  • [9] HORISBERGER JD, 1987, RENAL PHYSIOL BIOCH, V10, P198
  • [10] CLONING OR P57(KIP2), A CYCLIN-DEPENDENT KINASE INHIBITOR WITH UNIQUE DOMAIN-STRUCTURE AND TISSUE DISTRIBUTION
    LEE, MH
    REYNISDOTTIR, I
    MASSAGUE, J
    [J]. GENES & DEVELOPMENT, 1995, 9 (06) : 639 - 649