The Experts below are selected from a list of 1569 Experts worldwide ranked by ideXlab platform
Gang Wang - One of the best experts on this subject based on the ideXlab platform.
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Wilms tumor with inferior vena cava Duplication: a rare case report.
BMC Urology, 2018Co-Authors: Feng Guo, Wei Liu, Gang WangAbstract:Wilms tumor is the most common renal tumor of childhood. Duplication of the inferior vena cava is an uncommon anomaly. In the present study, we present a case of Wilms tumor with the inferior vena cava Duplication, which has not been reported previously. A 14-month-old female presented with an enlarging abdominal mass. Computed tomography imaging demonstrated a large mass in the right Kidney, Duplication of the inferior vena cava below the renal veins and compression of the right inferior vena cava caused by the enormous mass. A right radical nephrectomy was performed. Final pathology was consistent with Wilms tumor. Postoperative adjuvant chemotherapy was executed. Computed tomography imaging at 3 months postoperatively showed the right inferior vena cava played a dominant role and the left inferior vena cava was not detected clearly. During the follow-up of 18 months, no local recurrence or metastasis has been observed. It is important to recognize the case of Wilms tumor with the inferior vena cava Duplication to avoid injury of retroperitoneal venous anomalies and life-threatening hemorrhage during surgery through preoperative computed tomography.
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Wilms tumor with inferior vena cava Duplication: a rare case report
BMC, 2018Co-Authors: Feng Guo, Wei Liu, Gang WangAbstract:Abstract Background Wilms tumor is the most common renal tumor of childhood. Duplication of the inferior vena cava is an uncommon anomaly. In the present study, we present a case of Wilms tumor with the inferior vena cava Duplication, which has not been reported previously. Case presentation A 14-month-old female presented with an enlarging abdominal mass. Computed tomography imaging demonstrated a large mass in the right Kidney, Duplication of the inferior vena cava below the renal veins and compression of the right inferior vena cava caused by the enormous mass. A right radical nephrectomy was performed. Final pathology was consistent with Wilms tumor. Postoperative adjuvant chemotherapy was executed. Computed tomography imaging at 3 months postoperatively showed the right inferior vena cava played a dominant role and the left inferior vena cava was not detected clearly. During the follow-up of 18 months, no local recurrence or metastasis has been observed. Conclusion It is important to recognize the case of Wilms tumor with the inferior vena cava Duplication to avoid injury of retroperitoneal venous anomalies and life-threatening hemorrhage during surgery through preoperative computed tomography
Feng Guo - One of the best experts on this subject based on the ideXlab platform.
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Wilms tumor with inferior vena cava Duplication: a rare case report.
BMC Urology, 2018Co-Authors: Feng Guo, Wei Liu, Gang WangAbstract:Wilms tumor is the most common renal tumor of childhood. Duplication of the inferior vena cava is an uncommon anomaly. In the present study, we present a case of Wilms tumor with the inferior vena cava Duplication, which has not been reported previously. A 14-month-old female presented with an enlarging abdominal mass. Computed tomography imaging demonstrated a large mass in the right Kidney, Duplication of the inferior vena cava below the renal veins and compression of the right inferior vena cava caused by the enormous mass. A right radical nephrectomy was performed. Final pathology was consistent with Wilms tumor. Postoperative adjuvant chemotherapy was executed. Computed tomography imaging at 3 months postoperatively showed the right inferior vena cava played a dominant role and the left inferior vena cava was not detected clearly. During the follow-up of 18 months, no local recurrence or metastasis has been observed. It is important to recognize the case of Wilms tumor with the inferior vena cava Duplication to avoid injury of retroperitoneal venous anomalies and life-threatening hemorrhage during surgery through preoperative computed tomography.
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Wilms tumor with inferior vena cava Duplication: a rare case report
BMC, 2018Co-Authors: Feng Guo, Wei Liu, Gang WangAbstract:Abstract Background Wilms tumor is the most common renal tumor of childhood. Duplication of the inferior vena cava is an uncommon anomaly. In the present study, we present a case of Wilms tumor with the inferior vena cava Duplication, which has not been reported previously. Case presentation A 14-month-old female presented with an enlarging abdominal mass. Computed tomography imaging demonstrated a large mass in the right Kidney, Duplication of the inferior vena cava below the renal veins and compression of the right inferior vena cava caused by the enormous mass. A right radical nephrectomy was performed. Final pathology was consistent with Wilms tumor. Postoperative adjuvant chemotherapy was executed. Computed tomography imaging at 3 months postoperatively showed the right inferior vena cava played a dominant role and the left inferior vena cava was not detected clearly. During the follow-up of 18 months, no local recurrence or metastasis has been observed. Conclusion It is important to recognize the case of Wilms tumor with the inferior vena cava Duplication to avoid injury of retroperitoneal venous anomalies and life-threatening hemorrhage during surgery through preoperative computed tomography
Wei Liu - One of the best experts on this subject based on the ideXlab platform.
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Wilms tumor with inferior vena cava Duplication: a rare case report.
BMC Urology, 2018Co-Authors: Feng Guo, Wei Liu, Gang WangAbstract:Wilms tumor is the most common renal tumor of childhood. Duplication of the inferior vena cava is an uncommon anomaly. In the present study, we present a case of Wilms tumor with the inferior vena cava Duplication, which has not been reported previously. A 14-month-old female presented with an enlarging abdominal mass. Computed tomography imaging demonstrated a large mass in the right Kidney, Duplication of the inferior vena cava below the renal veins and compression of the right inferior vena cava caused by the enormous mass. A right radical nephrectomy was performed. Final pathology was consistent with Wilms tumor. Postoperative adjuvant chemotherapy was executed. Computed tomography imaging at 3 months postoperatively showed the right inferior vena cava played a dominant role and the left inferior vena cava was not detected clearly. During the follow-up of 18 months, no local recurrence or metastasis has been observed. It is important to recognize the case of Wilms tumor with the inferior vena cava Duplication to avoid injury of retroperitoneal venous anomalies and life-threatening hemorrhage during surgery through preoperative computed tomography.
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Wilms tumor with inferior vena cava Duplication: a rare case report
BMC, 2018Co-Authors: Feng Guo, Wei Liu, Gang WangAbstract:Abstract Background Wilms tumor is the most common renal tumor of childhood. Duplication of the inferior vena cava is an uncommon anomaly. In the present study, we present a case of Wilms tumor with the inferior vena cava Duplication, which has not been reported previously. Case presentation A 14-month-old female presented with an enlarging abdominal mass. Computed tomography imaging demonstrated a large mass in the right Kidney, Duplication of the inferior vena cava below the renal veins and compression of the right inferior vena cava caused by the enormous mass. A right radical nephrectomy was performed. Final pathology was consistent with Wilms tumor. Postoperative adjuvant chemotherapy was executed. Computed tomography imaging at 3 months postoperatively showed the right inferior vena cava played a dominant role and the left inferior vena cava was not detected clearly. During the follow-up of 18 months, no local recurrence or metastasis has been observed. Conclusion It is important to recognize the case of Wilms tumor with the inferior vena cava Duplication to avoid injury of retroperitoneal venous anomalies and life-threatening hemorrhage during surgery through preoperative computed tomography
Angelo Selicorni - One of the best experts on this subject based on the ideXlab platform.
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Renal tract ultrasonography and calcium homeostasis in Williams-Beuren syndrome
Pediatric Nephrology, 2002Co-Authors: Cinzia Sforzini, Donatella Milani, Emilio Fossali, Anna Barbato, Gianpaolo Grumieri, Mario G. Bianchetti, Angelo SelicorniAbstract:Renal ultrasound scan, circulating creatinine and calcium, and the urinary calcium excretion rate were investigated in 57 patients with clinically and genetically typical Williams-Beuren syndrome (25 female and 32 male subjects, aged from 1.0 year to 23 years, median 8.5 years) on regular follow up at our institution. Twenty-three unilateral abnormalities were detected in 20 patients: pelvic dilatation ( n =6), renal hypoplasia ( n =5), isolated renal cyst ( n =3), Kidney surface irregularity ( n =3), Kidney Duplication ( n =2), renal agenesis ( n =1), megaureter ( n =1), pelvic Kidney dystopia ( n =1), and renal stone ( n =1). Both infantile hypercalcemia and nephrocalcinosis was absent in the 57 patients. Mild hypercalcemia was noted in 1 and mild hypercalciuria in 2 patients after the 1st year of life. In conclusion, the study indicates the frequent occurrence of intrinsic renal tract abnormalities detected by ultrasonography in Williams-Beuren syndrome. However, the study does not confirm the importance given in the past to the occurrence of hypercalcemia and hypercalciuria.
Sy Park - One of the best experts on this subject based on the ideXlab platform.
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562 Radiological Evaluation of Pediatric Congenital Urinary Tract Anomalies
Archives of Disease in Childhood, 2012Co-Authors: Ss Hwang, Sy ParkAbstract:Purpose To illustrate a wide spectrum of congenital anomalies of the urinary tract in children. Materials and Methods We demonstrate radiological evaluation and its clinical significance of congenital anomalies of the urinary tract in pediatric patients. Results Demonstrated various pediatric congenital urological anomalies included Kidney (renal agenesis, ectopic Kidney, multicystic dysplastic Kidney, Duplication), ureter (primary megaureter, ectopic ureterocele, ectopic insertion of ureter), bladder (anterior bladder diverticulum), and urethra (posterior urethral valve, urethral diverticulum, urethral polyp). We also described its clinical significance. Conclusion Radiological evaluation including Ultrasonography, CT, and/or MRI is very useful for diagnosis and follow-up of pediatric urologic structural anomalies.
