scholarly journals A case report of a young girl with recurrent hematuria: a missed diagnosis - renal nutcracker syndrome

2019 ◽  
Vol 20 (1) ◽  
Author(s):  
Haifa Ali Bin Dahman ◽  
Ali Omer Aljabry
2019 ◽  
Vol 12 ◽  
pp. 117954761985538
Author(s):  
Nabil A Al-Zoubi

Purpose: The duodenum and the left renal vein (LRV) occupy the vascular angle made by the superior mesenteric artery (SMA) and the aorta. When the angle becomes too acute, compression of either structure can occur. Although superior mesenteric artery syndrome (SMAS) and renal Nutcracker syndrome (NCS) share the same pathogenesis, concurrent development has rarely been reported. Case report: A 38-year-old female patient with a past history of gastrojejunostomy operated 6 years ago due to SMAS. She referred to vascular clinic with sever intermittent left-sided loin pain during the last 6 years. Computed tomography (CT)-angiogram and selective LRV angiogram with pressure gradient confirmed the diagnosis of NCS. She was treated by LRV transposition with uneventful recovery and considerable relief of symptoms. Conclusions: NCS accompanying with SMAS is quite unusual. A patient, who first presents with clinical evidence of SMAS, could also simultaneously or sometime thereafter present with NCS and vice versa.


1969 ◽  
Vol 24 (3) ◽  
pp. 835-838 ◽  
Author(s):  
Harold R. Miller

A young girl whose WISC performance had declined from the normal to the moderately retarded range of intellectual ability over a 2-yr. period but who continued to function within the normal range in non-testing situations, was reinforced for giving correct answers on a readministration of the WISC. Monetary reward was effective in reestablishing WISC performance within the normal range. Some implications of this finding were discussed.


Author(s):  
Jacob Greenspan ◽  
David Szczerepa ◽  
Kaspar Trocha ◽  
Ajit Rao ◽  
Gabriella Fluss ◽  
...  

2017 ◽  
Vol 1 ◽  
pp. 107-110 ◽  
Author(s):  
Agnieszka Mroczkowska-Juchkiewicz ◽  
Jacek Postępski ◽  
Edyta Olesińska ◽  
Paulina Krawiec ◽  
Elżbieta Pac-Kożuchowska
Keyword(s):  

2019 ◽  
Vol 59 (9) ◽  
pp. 77-80
Author(s):  
Shingo Nakai ◽  
Tetsuo Watanabe ◽  
Yoshiyuki Nakano ◽  
Masashi Tsuda ◽  
Hiroyuki Sakakibara ◽  
...  

1970 ◽  
Vol 4 (1) ◽  
pp. 52-54
Author(s):  
Paban Kumar Sharma ◽  
Sujan Joshi

A young girl presented with a solid pelvic tumor, was found to be steroid cell tumor of ovary, is described herebecause of its rarity and its association with unexplained anemia which was spontaneously corrected after thetumor removal.Ovarian steroid cell tumor is known to account for approximately 0.1% of all ovarian neoplasms and isunfortunately seen to exerts malignant potentials although its association with multiple different endocrine orparaneoplastic changes are the main issues with affection to women of young as well.Key words: Steroid cell tumor; lipoid tumor.DOI: 10.3126/njog.v4i1.3334Nepal Journal of Obstetrics and Gynaecology June-July 2009; 4(1): 52-54


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