Results 51 to 60 of about 14,084 (155)
Mortality Patterns and Phenotypic Clusters in Trisomy 13: A Population‐Based Study From Japan
ABSTRACT Trisomy 13, the third most common autosomal trisomy after trisomy 21 and trisomy 18, is associated with a significantly high infant mortality rate. However, large‐scale studies examining causes of death in trisomy 13 remain scarce. Therefore, we aimed to better understand the mortality patterns.
Narumi Kato +2 more
wiley +1 more source
Significant haematuria caused by a pseudo-aneurysm in nephroblastoma
A 7-year-old boy presented with a nephroblastoma, frank haematuria and hypovolemic shock. The haemorrhage was controlled with embolization of the right renal artery and followed by a nephrectomy.
Jaques van Heerden +3 more
doaj +1 more source
EGR1 Nuclear Condensates Promote Renal Cyst Development in Polycystic Kidney Disease
ABSTRACT Autosomal dominant polycystic kidney disease (ADPKD) is marked by aberrant cell proliferation driven by cAMP‐PKA and MAPK signaling pathways. EGR1, a transcription factor directly activated by the above two pathways, is critical in the over‐proliferation of tumor cells, which share similarities with cystic epithelial cells in ADPKD. This study
Chaoqun Ren +15 more
wiley +1 more source
ABSTRACT Background and Aims The efficacy of anti‐adhesive barriers in preventing clinically significant adhesional small bowel obstruction (ASBO) in the pediatric population is poorly defined. This review seeks to evaluate the utility of anti‐adhesive barriers in pediatric populations undergoing abdominopelvic surgery.
Khang Duy Ricky Le +2 more
wiley +1 more source
Genomic Profiling of Pediatric Solid Tumors With a Dual DNA/RNA Panel: JCCG‐TOP2 Study
In the JCCG‐TOP2 nationwide pediatric cancer genomic profiling study, 204 patients' tumors and peripheral blood from 50 institutions across Japan were successfully analyzed using a dual DNA/RNA panel. A total of 147 (72%) had potentially actionable findings, including diagnostic, prognostic, and therapeutic findings in 111 (54%), 61 (30%), and 64 (31%),
Kayoko Tao +38 more
wiley +1 more source
ABSTRACT Background and Aims Bilateral Wilms tumor (BWT) presents a significant challenge in pediatric oncology, necessitating a delicate balance between achieving oncological control and preserving renal function. While nephron‐sparing surgery (NSS) has emerged as a promising alternative to radical nephrectomy, its overall safety and efficacy profile ...
Menna Sarhan +7 more
wiley +1 more source
The objective of this study is to assess standardized histograms of signal intensities of T2-weighted magnetic resonance image (MRI) modality before and after preoperative chemotherapy for nephroblastoma (Wilms’ tumor). All analyzed patients are enrolled
Sabine Müller +3 more
doaj +1 more source
Left picture: ERCP before stent placement. Right picture: ERCP after placement of two stents. Abstract Objectives Acute pancreatitis or obstruction is considered an indication for urgent surgery in patients with choledochal malformation. However, in this inflammatory stage, surgery can be challenging.
Johannes Weidner +6 more
wiley +1 more source
Nephroblastoma in a 51-year-old Male
Nephroblastoma is an uncommon renal malignancy primarily observed in the pediatric population, with its occurrence in adults being exceedingly infrequent.
Eldimson Bermudo +2 more
doaj +1 more source
Exploring Wilms Tumour: A Series of Four Cases [PDF]
Wilms tumour, or nephroblastoma, is a common neoplasm in children, with a mean age of incidence between 2-5 years and no sex predilection. The incidence accounts for approximately 7.8 cases per million children, with bilaterality occurring in 5-10% of ...
R Aiswarya +2 more
doaj +1 more source

