Macroscopic Haematuria in a 15-year old Male: A Case of Nutcracker Syndrome Managed by Endovascular Stenting

10.5580/5d3 ◽  
2007 ◽  
Vol 6 (2) ◽  
2016 ◽  
Vol 4 (2) ◽  
pp. 193-199 ◽  
Author(s):  
Ziheng Wu ◽  
Xiangtao Zheng ◽  
Yangyan He ◽  
Xin Fang ◽  
Donglin Li ◽  
...  

2011 ◽  
Vol 186 (2) ◽  
pp. 570-575 ◽  
Author(s):  
Shanwen Chen ◽  
Hongkun Zhang ◽  
Heng Shi ◽  
Lu Tian ◽  
Wei Jin ◽  
...  

2013 ◽  
Vol 76 (6) ◽  
pp. 350-353 ◽  
Author(s):  
Kuo-Kang Feng ◽  
Chun-Yang Huang ◽  
Chen-Yuan Hsiao ◽  
Tsung-Hsing Lee ◽  
Tzu-Ting Kuo ◽  
...  

2005 ◽  
Vol 42 (2) ◽  
pp. 275-280 ◽  
Author(s):  
Olivier Hartung ◽  
Dominique Grisoli ◽  
Mourad Boufi ◽  
Ivo Marani ◽  
Zaher Hakam ◽  
...  

2018 ◽  
Vol 52 (5) ◽  
pp. 355-356 ◽  
Author(s):  
Saroj Neupane ◽  
Nikhil Ambulgekar ◽  
Sushruth Edla ◽  
James Torey ◽  
Nithin Gottam ◽  
...  

2021 ◽  
Vol 14 (4) ◽  
pp. e240228
Author(s):  
Ana Sofia Esteireiro ◽  
Pedro Santos ◽  
Anabela Bicho

We describe a case of a 17-year-old man admitted in the emergency room with a 2-month history of intermittent macroscopic haematuria and left lumbar pain. Physical examination and vital signs were normal. Investigation indicated a recurrent non-glomerular haematuria. The Doppler ultrasound revealed a compression of the left renal vein with upstream dilatation which was subsequently confirmed by CT angiography. These findings are in keeping with a case of nutcracker syndrome (NutS). Although asymptomatic in most cases, it can be a rare cause of haematuria. The teenager was referred to paediatric nephrology and was treated conservatively with spontaneous resolution of macroscopic haematuria. With this case, we would like to highlight that in children or adolescents with haematuria without an apparent cause, a high level of suspicion and appropriate imaging are necessary for the diagnosis of NutS.


Vascular ◽  
2012 ◽  
Vol 20 (6) ◽  
pp. 337-341 ◽  
Author(s):  
Ryan Daily ◽  
Jerry Matteo ◽  
Todd Loper ◽  
Martin Northup

‘Nutcracker syndrome’ encompasses classical symptoms of hematuria and flank pain resulting from the compression of the left renal vein between the aorta and the superior mesenteric artery. In patients with unexplained left-sided hematuria, flank pain or non-specific abdominal pain, careful interrogation of diagnostic abdominal imaging should be performed to exclude the possibility of external compression on the left renal vein. The patient discussed in this case report is a 19-year-old woman with unilateral hematuria. Her symptoms started 13 months prior with nausea, lower abdominal pain and weight loss. Six months after the nausea began, she started having syncope, sometimes multiple episodes in one day. Syncope is one of the more rarely reported symptoms associated with nutcracker syndrome. As more cases are reported, endovascular repair is becoming an alternative treatment for nutcracker syndrome. The patient was treated with stenting of her left renal vein. At the three-week follow-up, she reported near resolution of nausea and abdominal pain. She had gained four pounds, no longer had gross hematuria and had had no episodes of syncope and her blood pressure had normalized. Endovascular specialists should be aware of the variety of symptoms that can occur with nutcracker syndrome, including syncope. The severity of these symptoms should guide the recommendation for intervention.


2013 ◽  
Vol 104 (6) ◽  
pp. 716-719
Author(s):  
Ryo Oka ◽  
Naoto Kamiya ◽  
Keiko Sugiura ◽  
Takumi Endo ◽  
Masashi Yano ◽  
...  

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