Download full-text PDF |
Source |
|---|
Publication Analysis
Top Keywords
Similar Publications
SURGICAL TREATMENT OF GASTRIC STUMP CANCER: A COHORT STUDY OF 51 PATIENTS.
Arq Bras Cir Dig
January 2025
Universidade Estadual de Campinas, Faculty of Medical Sciences, Department of Surgery, Digestive Diseases Surgical Unit - Campinas (SP), Brazil.
Background: Gastric stump neoplasia is defined as a neoplasia that arises in the gastric remnant after at least 5 years of interval from the first gastric resection.
Aims: The aim of this study was to analyze 51 patients who underwent total and subtotal gastrectomy and multi-visceral resections in patients with gastric stump cancer.
Methods: The hospital records of 51 patients surgically treated for gastric stump cancer between 1989 and 2019 were reviewed.
The Readiness Imperative: Leveraging Large Animal Resident Research to Enhance Expeditionary Surgical Skills.
Mil Med
September 2024
Department of Surgery, UC Davis Medical Center, Sacramento, CA 95817, USA.
Article Synopsis
- The Defense Health Agency wants to ensure military surgical residents gain necessary skills for combat environments while supporting research through Clinical Investigation Programs (CIPs).
- A study analyzed large animal protocols from a Combat Casualty Care Research Program (CCCRP) over five years, focusing on various surgical procedures performed by residents.
- Results showed a total of 8,676 surgical procedures and significant research achievements, including national presentations, research awards, and publications, highlighting residents' critical care experience with trauma and surgical interventions.
Paraneoplastic Syndrome in Adrenocortical Carcinoma: The Unexpected Mime.
Cureus
June 2024
Pathology, Jefferson Einstein Philadelphia Hospital, Philadelphia, USA.
Adrenocortical carcinoma (ACC) is a malignancy of the adrenal cortex with a high morbidity and mortality. More than half of the cases are functional tumors. As different hormones can be co-secreted above physiologic levels, it causes a very broad variety of symptoms and makes differentiating from more common entities hard.
View Article and Find Full Text PDFPancreatic neuroendocrine tumor with solitary splenic metastasis and synchronous renal cell carcinoma: A rare case report.
Radiol Case Rep
July 2024
Addis Ababa University, College of Health Sciences, Department of Radiology, Addis Ababa, Ethiopia.
Synchronous pancreatic neuroendocrine tumors and renal cell cancer are extremely rare. Von-Hipple-Landau syndrome is a major association. A 43-year-old male patient with left upper quadrant pain and significant weight loss was diagnosed with a synchronous pancreatic tail neuroendocrine tumor with solitary splenic metastasis and a clear-cell renal cell carcinoma of the left kidney.
View Article and Find Full Text PDFSevere hepatic sinusoidal obstruction syndrome in a patient with Wilms tumor and hereditary spherocytosis.
Int Cancer Conf J
April 2024
Department of Pediatrics, Sisli Hamidiye Etfal Training and Research Hospital, University of Health Sciences, Istanbul, Turkey.
A 7-year-old girl with a history of splenectomy for hereditary spherocytosis (HS) was diagnosed with renal hematoma after a blunt abdominal trauma while receiving aspirin. Multiple erythrocyte transfusions and transarterial embolization were performed without success. Eventual nephrectomy revealed severely necrotic and perforated Stage III Wilms tumor (WT).
View Article and Find Full Text PDFWant AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!