Revascularization in a 17-Year-Old Girl with Neurofibromatosis

被引:4
|
作者
Beladan, Carmen C. [1 ,2 ]
Geavlete, Oliviana D. [1 ,2 ]
Botezatu, Simona [2 ]
Postu, Marin [2 ]
Popescu, Bogdan A. [1 ,2 ]
Ginghina, Carmen [1 ,2 ]
Coman, Ioan M. [1 ,2 ]
机构
[1] Univ Med & Pharm Carol Davila, Dept Cardiol, Bucharest 050474, Romania
[2] Inst Cardiovasc Dis Prof Dr CC Iliescu, Dept Cardiol, Bucharest 022328, Romania
来源
TEXAS HEART INSTITUTE JOURNAL | 2017年 / 44卷 / 01期
关键词
Blood pressure monitoring; ambulatory/methods; hypertension; renovascular/diagnosis/etiology/radiography/therapy; neurofibromatosis; 1/complications/metabolism/pathology; renal artery obstruction/complications/pathology/therapy; treatment outcome; vascular diseases/physiopathology; RENAL-ARTERY STENOSIS; MANAGEMENT; DISEASE; TYPE-1; ANGIOPLASTY;
D O I
10.14503/THIJ-15-5466
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Renal artery stenosis caused by neurofibromatosis is a rare cause of renovascular hypertension. This hypertension can develop during childhood and is one of the leading causes of poor outcome. We report the case of a 17-year-old girl who was incidentally diagnosed with severe hypertension. During her examination for secondary hypertension, we reached a diagnosis of neurofibromatosis type 1 on the basis of a cluster of typical findings: optic nerve glioma, cafe au lait spots, nodular neurofibromas, and axillary freckling. Renal angiograms revealed a hemodynamically significant left renal artery stenosis (70%). Renal angioplasty with a self-expanding stent was performed one month later for rapidly progressive renal artery stenosis (90%) and uncontrolled blood pressure. Excellent blood pressure control resulted immediately and was maintained as of the 2-year followup evaluation. We think that percutaneous transluminal renal angioplasty can be effective in select patients who have neurofibromatosis type 1 and refractory hypertension caused by renal artery stenosis.
引用
收藏
页码:50 / 54
页数:5
相关论文
共 50 条
  • [1] NECROPHILIA IN A 17-YEAR-OLD GIRL
    FOERSTER, K
    FOERSTER, G
    ROTH, E
    [J]. SCHWEIZER ARCHIV FUR NEUROLOGIE UND PSYCHIATRIE, 1976, 119 (01): : 97 - 107
  • [2] Parotid Sialolithiasis in a 17-Year-Old Girl
    Almotairi, Nawaf
    Alotaibi, Mohammad
    Aldaihani, Manal
    Almutairi, Mishal
    [J]. CUREUS JOURNAL OF MEDICAL SCIENCE, 2023, 15 (03)
  • [3] Anemia in a 17-Year-Old Hispanic Girl
    Bhatia, Erin G.
    Markowitz, Jonathan E.
    [J]. CLINICAL GASTROENTEROLOGY AND HEPATOLOGY, 2013, 11 (08) : XXIV - XXIV
  • [4] Suicidality and Melancholia in a 17-Year-Old Girl
    Airuehia, Efosa
    Adam, Balkozar
    [J]. PSYCHIATRIC ANNALS, 2014, 44 (08) : 363 - 364
  • [5] A 17-Year-Old Girl with a Black Eschar
    Strenger, Volker
    Mueller, Martin
    Richter, Susanne
    Revilla-Fernandez, Sandra
    Nitsche, Andreas
    Klee, Silke R.
    Ellerbrok, Heinz
    Zenz, Werner
    [J]. CLINICAL INFECTIOUS DISEASES, 2009, 48 (01) : 91 - 92
  • [6] Knee Pain in a 17-year-old Girl
    Chaabane, Skander
    Merghani, Amira
    Drissi, Cyrine
    Ladeb, Mohamed Fethi
    [J]. CLINICAL ORTHOPAEDICS AND RELATED RESEARCH, 2010, 468 (07) : 2003 - 2006
  • [7] Exfoliation syndrome in a 17-year-old girl
    Konstas, AGP
    Ritch, R
    Bufidis, T
    Morales, J
    Streeten, BW
    [J]. ARCHIVES OF OPHTHALMOLOGY, 1997, 115 (08) : 1063 - 1067
  • [8] A 17-year-old girl with fever and lymphadenopathy
    Wheaton, Laura
    Punnett, Angela
    Baker, Jillian M.
    [J]. PAEDIATRICS & CHILD HEALTH, 2018, 23 (01) : 3 - 5
  • [9] CARCINOMA OF TONGUE IN A 17-YEAR-OLD GIRL
    ELLIS, H
    [J]. PROCEEDINGS OF THE ROYAL SOCIETY OF MEDICINE-LONDON, 1966, 59 (09): : 858 - &
  • [10] Multiple intracerebral metastases of a 17-year-old girl with previously diagnosed neurofibromatosis type I
    Maschke, M
    Kastrup, O
    Reinhardt, V
    Keidel, M
    [J]. CLINICAL NEUROPATHOLOGY, 1999, 18 (01) : 42 - 44