Results 21 to 30 of about 7,429 (165)

Splenectomy in Sickle Cell Haemoglobinopathies from a Tertiary Hospital of Southern Odisha: A Retrospective Study [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2022
Introduction: Sickle Cell Disease (SCD) is a common haemoglobinopathy, where spleen is considered to be the first organ to be involved. Although it initially undergoes enlargement, but most often there occurs autosplenectomy. But in some cases, there
Abinash Kumar Panda   +3 more
doaj   +1 more source

Klippel–Trenaunay–Weber syndrome with atypical presentation of hypersplenism and nephrotic syndrome: a case report

open access: yesJournal of Medical Case Reports, 2017
Background Klippel–Trenaunay–Weber syndrome is a rare syndrome; unfortunately, very few studies of the connection between hypersplenism, nephrotic syndrome, and Klippel–Trenaunay–Weber syndrome have been published. Case presentation We report the case of
Linda Kundzina, Sandra Lejniece
doaj   +1 more source

Clinical observation and risk assessment after splenectomy in hepatolenticular degeneration patients associated with hypersplenism

open access: yesFrontiers in Surgery, 2022
BackgroundBoth hepatolenticular degeneration (HLD) and viral hepatitis B (HBV) can cause hypersplenism, but whether splenectomy is needed or can be performed in HLD patients associated with hypersplenism is still controversial.
Wanzong Zhang   +9 more
doaj   +1 more source

Change in platelet count in patients with hypersplenism subjected to liver transplantation

open access: yesArquivos de Gastroenterologia, 2011
CONTEXT: Most patients subjected to liver transplantation presents hypersplenism, which is reversed after the operation. However, some patients remain with moderate to intense hypersplenism.
Júlio Cezar Uili Coelho   +5 more
doaj   +1 more source

Granulomatous Liver Disease in Ataxia-Telangiectasia With the Hyper-IgM Phenotype: A Case Report

open access: yesFrontiers in Pediatrics, 2020
Ataxia-telangiectasia (A-T) is an autosomal recessive disorder characterized by neurodegeneration, combined immunodeficiency, and oculocutaneous telangiectasia. The hyper-IgM phenotype of A-T, correlating with a class-switch recombination defect, IgG and
Aleksandra Szczawińska-Popłonyk   +2 more
doaj   +1 more source

Percutaneous splenic embolization of the splenic artery in the treatment of hypersplenism.

open access: yesActa Médica Portuguesa, 1992
Percutaneous splenectomy was performed in 6 patients with hypersplenism. Peripheral blood cell counts improved in 5 of the patients. The authors review the indications, technique and complications of percutaneous splenic embolization.
J M Pisco   +3 more
doaj   +1 more source

Coexistence of immunophenotypically normal and aberrant mast cells in patients with clonal mast cell diseases associates with more indolent subtypes and less severe disease characteristics

open access: yesCytometry Part B: Clinical Cytometry, EarlyView.
Abstract Aberrant antigen expression on mast cells (MCs) is one of the most accurate diagnostic markers for clonal MC diseases (CMCD). Although the coexistence of normal and pathologic MCs is frequently seen, the disease characteristics associated with it have been minimally investigated.
Abdulrazzaq Alheraky   +6 more
wiley   +1 more source

Comparative evaluation of laparoscopic splenectomy versus open splenectomy

open access: yesZaporožskij Medicinskij Žurnal, 2018
The aim of research: to study the short-term treatment results in patients with blood diseases, portal hypertension, pathology of the spleen who underwent laparoscopic splenectomy based on the surgical indications in comparison with the treatment results
H. I. Okhrimenko   +4 more
doaj   +1 more source

Engineered molecular diagnostic strategies for hepatocellular carcinoma: Integrating flexible photonic barcodes, liquid biopsies, and AI‐enhanced sensing platforms

open access: yesFlexMat, EarlyView.
Abstract Early diagnosis of hepatocellular carcinoma (HCC) remains challenging because conventional serum biomarkers, especially alpha‐fetoprotein (AFP), show limited sensitivity for early‐stage disease. Recent progress in engineered molecular diagnostics provides new opportunities to improve HCC detection through integrated material, molecular, and ...
Jingzhi Xue   +5 more
wiley   +1 more source

Home - About - Disclaimer - Privacy