2.Amyloidosis of the unilateral renal pelvis, ureter and urinary bladder: a case report.
Chinese Medical Sciences Journal 2011;26(3):197-200
Aged
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Amyloidosis
;
diagnosis
;
pathology
;
Humans
;
Kidney Pelvis
;
pathology
;
Male
;
Ureter
;
pathology
;
Urinary Bladder
;
pathology
3.Magnetic resonance urography and X-ray urography findings of congenital megaureter.
Tian-Ran LI ; Xiang-Ke DU ; Tian-Long HUO
Chinese Medical Sciences Journal 2011;26(2):103-108
OBJECTIVETo observe the imaging findings of congenital megaureter in order to enhance the understanding of this disease.
METHODSImage data of 5 patients with congenital megaureter and 2 misdiagnosed patients were analyzed, and image findings of congenital megaureter were summarized.Elscint Prestig 2.0T superconductive magnetic resonance urography (MRU) with conventional sequence (spin-echo, T1WI560 ms/16 ms; fast spin-echo, T2WI 9600 ms/96 ms ) was performed. Raw data were acquired with fastspin-echo sequence from heavy T2-weighted image (9600 ms/120 ms). Post-processing method of MRU was the maximum intensity projection with three-dimensional reconstruction in the workstation. Intravenous pyelography (IVP) was conducted, in which X-rayfilms were taken 7 minutes, 15 minutes, and 30 minutes after injecting contrast agent, exceptthat in 2 patients the films were taken delayed at 60 and 90 minutes .X-ray retrograde pyelography was performed on 2 patients, successful in one butfailed in the other.
RESULTSThe dilated ureter showed hypointensity on T1-weighted images and hyperintensity on T2-weighted images in conventional MRI. The mass wall was intact, uniform in thickness, and showing hypointensity on T1-weighted and T2-weighted images. The MRU images showed a retroperitoneal mass appearing as an elongated tubular cystic structure spreading from kidney to bladder. MRU also revealed dilated calices and renal pelvis, pelviureteric obstruction, and renal duplication. The main signs of congenital megaureter in X-urography was significant dilatation of ureter, or normal renal pelvis with ureter dilatation, hydronephrosis, deformity, and displacement.
CONCLUSIONSMRU with X-urography could visualizethe characteristics of congenital megaureter, including the dilation of renal pelvis and ureter, calculi, urinary tract duplication, and stenosis location. The two techniques can complement each other in disease diagnosis and provide more detailed information for preoperative treatment.
Humans ; Magnetic Resonance Imaging ; methods ; Ureter ; abnormalities ; pathology ; Urography
5.A rare case of localised AA-type amyloidosis of the ureter with spheroids of amyloid.
Sangeeta MANTOO ; Jacqueline Siok Gek HWANG ; Gilbert Shin Chuin CHIANG ; Puay Hoon TAN
Singapore medical journal 2012;53(4):e77-9
We present a case of localised AA-type amyloidosis of the ureter with spheroids of amyloid. Localised AA-type amyloidosis of the urogenital tract is uncommon and extremely rare as a cause of ureteric obstruction, with only two such cases described in the literature to date. Most previously described cases at this site are related to primary AL-type amyloidosis. Another interesting finding in this case is the presence of spheroids of amyloid, which to the best of our knowledge, has not been previously reported at this site, and is also unusual at other sites.
Adult
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Amyloid
;
analysis
;
Amyloidosis
;
pathology
;
Female
;
Humans
;
Ureter
;
pathology
;
Ureteral Diseases
;
pathology
6.Laparoscopic treatment of a massive fibroepithelial polyp accompanied by ureteral intussusception.
Xun-Bo JIN ; Hui-Lin MENG ; Yang-de ZHANG ; Shao-Bo JIANG ; Han-Bo WANG ; Jin WANG
Chinese Medical Journal 2011;124(20):3436-3439
Ureteral fibroepithelial polyp accompanied by intussusception is a rare occurrence. Currently, most ureteral polyps could be removed readily by ureteroscopy. Nevertheless, endoscopic resection can be difficult in patient with a large polyp, especially accompanied by an intussusception. We described our experience and laparoscopic technique for treatment of a symptomatic 63-year-old woman who presented with a pedunculated, 9-cm-long, left lower ureteral, fibroepithelial polyp accompanied by a 2-cm-long intussusception.
Female
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Humans
;
Intussusception
;
pathology
;
surgery
;
Laparoscopy
;
methods
;
Middle Aged
;
Polyps
;
pathology
;
surgery
;
Ureter
;
pathology
;
surgery
7.Comment on: A rare case of localised AA-type amyloidosis of the ureter with spheroids of amyloid.
Singapore medical journal 2012;53(8):560-author reply 560
Amyloid
;
analysis
;
Amyloidosis
;
pathology
;
Female
;
Humans
;
Ureter
;
pathology
;
Ureteral Diseases
;
pathology
8.Idiopathic retroperitoneal fibrosis misdiagnosed as renal cancer: a case report and literature review.
Weining WANG ; Yanbo WANG ; Xiaobo MA ; Haidong YU ; Chunxi WANG
Journal of Southern Medical University 2014;34(11):1658-1660
A 51-year-old male patient was presented to our hospital for inspection of right renal space-occupying lesions. CT revealed soft tissue density in the right renal pelvis and renal pelvis ureter transitional crumb, for which a clinical diagnosis of right renal cancer was made. After laparoscopic radical resection of the right kidney, pathological examination supported the diagnosis of idiopathic retroperitoneal fibrosis. With an unclear pathogenesis, idiopathic retroperitoneal fibrosis presents with atypical clinical manifestations but shows specific features in imaging examination. Its treatment is individualized according to the specific condition for which conservative medical or surgical treatment can be considered. Retroperitoneal fibrosis has a low incidence and a high misdiagnosis rate, and imaging examinations remain currently the primary modality for diagnosis with specific findings.
Diagnostic Errors
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Humans
;
Kidney Neoplasms
;
Kidney Pelvis
;
pathology
;
Male
;
Middle Aged
;
Retroperitoneal Fibrosis
;
diagnosis
;
Ureter
;
pathology
9.Investigation on factors related to pyelic separation in early newborns.
Qian ZHANG ; Yan LI ; Xiao HE ; Shu-Ling XU ; Hong-Xiang GUO ; Xin-Ru CHENG
Chinese Journal of Contemporary Pediatrics 2012;14(10):742-745
OBJECTIVETo explore the relationship of pyelic separation with gestational age, body weight and sex in early newborns.
METHODSA total of 320 neonates were examined by renal ultrasound 2-7 days after birth. The neonates included 180 boys and 140 girls, with a mean gestational age of 36±3 weeks (28-42 weeks) and a mean birth weight of 2430±1000 g (900-4870 g). Correlation analysis was performed between renal pelvis anteroposterior diameter (APD) and gestational age/body weight. The newborns were grouped based on gestational age, body weight and sex and the incidence of pyelic separation was compared among the groups.
RESULTSPyelic separation was found in 100 of the 320 newborns. The incidence of pyelic separation in boys (37.8%, 70 cases) was significantly higher than in girls (22.2%, 30 cases) (P<0.05). The incidence rates of pyelic separation on the left side, right side and both sides were 59%, 13% and 29% respectively in boys, and 53%, 7% and 40% respectively in girls. There was no significant difference in the location of renal pelvis separation between boys and girls (P>0.05). There significant difference in the incidence of pyelic separation between different gestational age groups (P>0.05). APD was positively correlated with gestational age and birth weight (P<0.05). The incidence of pyelic separation was negatively correlated with birth weight in all newborns except those who were macrosomic (P<0.05).
CONCLUSIONSThe incidence of pyelic separation in early newborns is closely associated with birth weight and sex. APD is positively correlated to gestational age and birth weight. Pyelic separation often occurs more frequently on the left side or both sides than on the right side.
Birth Weight ; Female ; Gestational Age ; Humans ; Infant, Newborn ; Kidney Pelvis ; pathology ; Male ; Ureter ; pathology
10.Fibroepithelial ureteral polyp: a case report; endoscopic removal of large ureteral polyp.
Heeyoul KIM ; Duk Kyo KIM ; Sun Ju LEE ; Sung Goo CHANG
Journal of Korean Medical Science 1996;11(1):80-83
We report a case of primary fibroepithelial polyp of the right midureter. The patient was a 41-year-old-woman, complaining of right flank pain. An excretory urogram revealed right hydronephrosis and a filling defect of the the right midureter. The filling defect was produced by a large fibroepithelial polyp that was diagnosed and removed by ureteroscopy without open surgery. Large fibroepithelial ureteral polyps are relatively rare and ureteroscopy is the gold standard of diagnosis for ureteral filling defect.
Adult
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Case Report
;
*Endoscopy
;
Female
;
Human
;
Polyps/pathology/*surgery
;
Ureter/pathology/*surgery
;
Ureteral Neoplasms/pathology/*surgery
;
Ureteroscopy