Results 11 to 20 of about 1,184,867 (159)

Optimal biliary drainage for inoperable Klatskin's tumor based on Bismuth type. [PDF]

open access: yesWorld J Gastroenterol, 2007
AIM: To investigate differences in the effects of biliary drainage procedures in patients with inoperable Klatskin's tumor based on Bismuth type, considering endoscopic retrograde biliary drainage (ERBD), external percutaneous transhepatic biliary ...
Lee SH   +6 more
europepmc   +2 more sources

Sister Mary Joseph's Nodule Revealing Klatskin's Cholangiocarcinoma at the Yalgado Ouedraogo University Hospital: Case Report and Literature Review. [PDF]

open access: yesClin Case Rep
ABSTRACT Umbilical cutaneous metastases of abdomino‐pelvic tumors are rare. They are known as Sister Mary Joseph nodules. The presence of this nodule indicates an advanced cancerous lesion and is associated with a poor prognosis. Because of its rarity, the Sister Mary Joseph nodule can go unnoticed.
Ky LJE   +11 more
europepmc   +2 more sources

Efficacy and safety of endoscopic ultrasonography (EUS) hepaticogastrostomy (HGS) versus choledochoduodenostomy (CDS) in ERCP-failed malignant biliary obstruction: A systematic review and META-analysis. [PDF]

open access: yesJGH Open
Abstract Endoscopic retrograde cholangiopancreatography (ERCP) is the gold standard in managing malignant biliary obstruction. The success of ERCP has limitations, whereas surgical biliary bypass and percutaneous transhepatic approaches, as alternative modalities, come with significant costs, longer durations, and higher levels of mortality and ...
Rizqiansyah CY   +4 more
europepmc   +2 more sources

Splenic artery steal syndrome after liver transplantation: A case series and review of literature. [PDF]

open access: yesClin Case Rep
Key Clinical Message Splenic steal syndrome (SASS) represents a challenge to interventional radiologists after orthotopic liver transplantation. In this case series, we present three cases of patients who developed SASS after their liver transplants.
Saad Eddin A   +5 more
europepmc   +2 more sources

Dysembryoplastic Neuroepithelial Tumor: A Benign but Complex Tumor of the Cerebral Cortex [PDF]

open access: yes, 2022
Dysembryoplastic neuroepithelial tumor (DNET) is a distinct type of low-grade glioneuronal tumor. Clinically, DNET is highly associated with intractable epilepsy in young children and adolescents.
김세훈
core   +1 more source

The Korean Society for Neuro-Oncology (KSNO) guideline for antiepileptic drug usage of brain tumor: Version 2021.1 [PDF]

open access: yes, 2021
Background: To date, there has been no practical guidelines for the prescription of antiepileptic drugs (AEDs) in brain tumor patients in Korea. Thus, the Korean Society for Neuro-Oncology (KSNO), a multidisciplinary academic society, had begun preparing
김세훈, 윤홍인, 장종희
core   +1 more source

A National Consensus Survey for Current Practice in Brain Tumor Management I: Antiepileptic Drug and Steroid Usage [PDF]

open access: yes, 2020
Background: The Guideline Working Group of the Korean Society for Neuro-Oncology (KSNO) conducted a nationwide questionnaire survey for diverse queries faced in the treatment of brain tumors. As part I of the survey, the aim of this study is to evaluate
김세훈, 윤홍인, 장종희
core   +1 more source

Current progress in robotic hepatobiliary and pancreatic surgery at a high‐volume center

open access: yesAnnals of Gastroenterological Surgery, Volume 7, Issue 6, Page 863-870, November 2023., 2023
Our institution was one of the first in the world to perform robotic HPB surgeries. This review of our institutions experience, as well as a review of current international progress in robotic HPB surgery, may provide insight for aspiring HPB surgeons who wish to incorporate robotics. Abstract There has been steady growth in the adoption of robotic HPB
Frances N. McCarron   +2 more
wiley   +1 more source

Genome sequencing identifies complex structural MLH1 variant in unsolved Lynch syndrome

open access: yesMolecular Genetics &Genomic Medicine, Volume 11, Issue 6, June 2023., 2023
A family with Lynch syndrome is presented by this article. Standard diagnostic tests, such as panel or exome sequencing, were unable to detect the underlying copy‐number neutral structural genetic variant in MLH1. This case aims to illustrate the advantages of clinical genome sequencing in routine diagnostics in detecting structural variants.
Dennis Witt   +11 more
wiley   +1 more source

Intracranial Extraskeletal Myxoid Chondrosarcoma in Fourth Ventricle [PDF]

open access: yes, 2021
We present an extremely rare case of intracranial extraskeletal myxoid chondrosarcoma. A 36-year-old male presented with dizziness persisting for 2 weeks. MRI of the patient showed well-enhanced mass of fourth ventricle.
김세훈, 장종희, 유지환
core   +1 more source

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