A5061935486- Congenital Diaphragmatic Hernia Studies
- Teratomas and Epidermoid Cysts
- Vascular Malformations and Hemangiomas
- Urologic and reproductive health conditions
- Childhood Cancer Survivors' Quality of Life
- Lymphatic Disorders and Treatments
- Central Venous Catheters and Hemodialysis
- Intestinal Malrotation and Obstruction Disorders
- Urological Disorders and Treatments
- Tumors and Oncological Cases
- Pleural and Pulmonary Diseases
- Infectious Diseases and Tuberculosis
- Dialysis and Renal Disease Management
- Soft tissue tumor case studies
- Neuroblastoma Research and Treatments
- Pediatric Hepatobiliary Diseases and Treatments
- Esophageal and GI Pathology
- Sarcoma Diagnosis and Treatment
- Cystic Fibrosis Research Advances
- Acute Kidney Injury Research
- Anorectal Disease Treatments and Outcomes
- Head and Neck Surgical Oncology
- Hyperglycemia and glycemic control in critically ill and hospitalized patients
- Spinal Dysraphism and Malformations
- Congenital gastrointestinal and neural anomalies
Chiba University
2024
National Center For Child Health and Development
2021-2023
To elucidate the clinical significance of sarcopenia in children with neuroblastic tumors (NTs).
Abstract Background Pleuroperitoneal communication (PPC) is an uncommon, but potentially life-threatening complication of peritoneal dialysis (PD). If a fistula does not close with conservative treatment, surgical repair required. However, approximately half these patients are forced to shift from PD hemodialysis. Although it important confirm the site achieve successful this identification more difficult in pediatric than adults. Case presentation We report two infantile cases severe PPC...
Yolk sac tumor (YST) is a germ cell that generally associated with good prognosis in children. It has been recently reported vaginal YSTs can be cured using chemotherapy alone. Thus, minimal invasiveness and function preservation are pre-requisites for surgical approaches. Herein, we report case of YST was resected function-preserving manner unique combination In 9-month-old Asian female infant, detected while investigating bleeding. The patient referred to our hospital, the diagnosed as...
<title>Abstract</title> <bold>Purpose</bold> To elucidate the clinical significance of sarcopenia in children with neuroblastic tumors (NTs).<bold>Methods</bold> We conducted a retrospective observational study and analyzed z-scores for height, body weight, mass index, skeletal muscle index (HT-z, BW-z, BMI-z, SMI-z) along characteristics 36 NTs. SMI-z was calculated from 138 computed tomography scans at diagnosis, during treatment, follow-up. The International Neuroblastoma Risk Group...
We report a case of one-year-old boy with congenital dermal sinus situated at the lateral buttock. The exact pathway was shown by magnetic resonance imaging, contrast medium examination and computed tomographic examination. not connected to spinal canal ended near anterior surface sacral bone in blind manner. Complete surgical resection achieved after these imaging examinations.
Cellulitis is a common complication of cystic lymphatic malformations (cLM) and Klippel–Trenaunay syndrome (KTS). in the pediatric population requires hospitalization reduces patients' quality life. This study aimed to clarify seasonality characteristics cellulitis patients with cLM KTS. We retrospectively reviewed clinical records KTS who were admitted for between January 2014 December 2021. One hundred seventeen hospitalizations 33 examined. There 80 37 oatients, respectively. The number...
ABSTRACT Background This study aimed to investigate and compare the applied treatments prognosis between patients with congenital acquired onset cystic lymphatic malformation (cLM). Methods was a retrospective cohort in single hospital. Patients cLM treated at our institution were included this study, divided into those diagnosed utero or birth (CO) later after (AO) emerged lesion. Age, site, size of lesion, histological subtype, invasiveness grade treatment, treatment outcomes compared....
Congenital H-type fistula is a rare congenital rectourogenital anomaly and less common in males than females. A one-year-and-eight-month-old boy with an ectopic perineal was incidentally diagnosed when he underwent voiding cystourethrography for vesicoureteral reflux. Further examination revealed that the ano-bulbar urethral fistula. At two years of age, patient fistulectomy also anterior sagittal anorectoplasty during same surgery.
Triple duodenal obstruction is an extremely rare disorder—apparently only two cases were reported in the English literature. We present a third case complicated with some cardiovascular anomalies (interrupted inferior vena cava, left-sided preduodenal portal vein, and ventricular septal defect) intestinal malrotation. Operative procedure to reconstruct continuity of lumen was combination longitudinal incision, partial web resection, transverse closure at first site together diamond-shaped...
Outflow obstruction of a catheter for peritoneal dialysis (PD) is one the most common complications in patients who are undergoing PD renal failure. Although cause variable, choked caused by fallopian tube fimbria quite rare and only five pediatric cases were reported. We report case five-month-old female suffered from recurrent fimbria. Laparoscopic surgery was performed to recanalize catheter, but recurred three days after surgery. abandoned use that had been inserted into Douglas fossa...