ABSTRACT
The most recent version of the European Society for Medical Oncology (ESMO) Clinical Practice Guidelines for the diagnosis, treatment and follow-up of patients with endometrial cancer was published in 2022. It was therefore decided, by both the ESMO and the Indian Society of Medical and Paediatric Oncology (ISMPO), to convene a virtual meeting in July 2022 to adapt the ESMO 2022 guidelines to take into account the variations in the management of endometrial cancer in Asia. These guidelines represent the consensus opinion of a panel of Asian experts representing the oncological societies of China (CSCO), India (ISMPO), Indonesia (ISHMO), Japan (JSMO), Korea (KSMO), Malaysia (MOS), the Philippines (PSMO), Singapore (SSO), Taiwan (TOS) and Thailand (TSCO). Voting was based on scientific evidence and was conducted independently of the current treatment practices and treatment access constraints in the different Asian countries, which were discussed when appropriate. The aim of this guideline manuscript is to provide guidance for the optimisation and harmonisation of the management of patients with endometrial cancer across the different regions of Asia, drawing on the evidence provided by Western and Asian trials whilst respecting the variations in clinical presentation, diagnostic practices including molecular profiling and disparities in access to therapeutic options, including drug approvals and reimbursement strategies.
Subject(s)
Endometrial Neoplasms , Societies, Medical , Child , Female , Humans , Asia , Endometrial Neoplasms/diagnosis , Medical OncologyABSTRACT
Jejunal diverticulosis, a form of acquired false diverticula, is considered to be a rare clinical entity, which is mostly asymptomatic. But, in case of complications, jejunal diverticulosis can present as acute abdominal distress. Due to its rarity in clinical manifestation, jejunal diverticulosis may lead to a diagnostic and therapeutic delay. We report on 3 interdisciplinary cases of complicated jejunal diverticulosis by diverticulitis, diverticular bleeding, and perforation. We want to highlight the fact that complicated jejunal diverticulosis should be considered as a differential diagnosis in cases of unclear abdominal pain.
Subject(s)
Abdominal Pain/diagnosis , Abdominal Pain/etiology , Diverticulum/complications , Diverticulum/diagnosis , Intestine, Small/abnormalities , Aged , Diagnosis, Differential , Female , Humans , Jejunal Diseases , Male , Middle Aged , Pain Measurement/methods , Rare Diseases/complications , Rare Diseases/diagnosisSubject(s)
Fumarates/therapeutic use , Graft Rejection/prevention & control , Kidney Transplantation/physiology , Acute Disease , Animals , Chronic Disease , Creatinine/blood , Drug Evaluation, Preclinical , Graft Rejection/blood , Rats , Rats, Inbred F344 , Rats, Inbred WF , Time Factors , Transplantation, HomologousABSTRACT
Impaired healing induced by leakage of bile has been postulated as one factor responsible for complications after reconstructive bile duct surgery. The cytotoxicity of human bile and its major bile acids on cultured human fibroblasts was therefore studied by evaluation of their effects on cell morphology and growth, on synthesis and secretion of 35SO4-mucopolysaccharides and on release of a lysosomal enzyme. Normal human fibroblasts derived from a standard culture strain (MRC-5) were grown to confluence and exposed to: (1) sterile human T-tube bile, (2) a mixture of bile acids resembling that of human bile, or (3) various concentrations of the glycine- and taurine conjugates of cholic, chenodeoxycholic or deoxycholic acid. Medium containing whole bile (total bile acid concentration 0.25, 0.75 or 1.6 mmol/l) exerted time and dose dependent cytotoxic effects on morphology and growth and release of lysosomal enzyme. Synthesis and secretion of 35SO4-mucopolysaccharides were markedly inhibited. The bile acid mixture exhibited the same time and dose dependent effects. The conjugates of deoxycholic acid were found to be the most toxic of the individual bile acids studied.
Subject(s)
Bile Acids and Salts/pharmacology , Bile/physiology , Fibroblasts/drug effects , Bile Acids and Salts/toxicity , Cells, Cultured , Cerebroside-Sulfatase/metabolism , Culture Media , Fibroblasts/metabolism , Fibroblasts/pathology , Glycosaminoglycans/metabolism , Humans , In Vitro Techniques , Membrane Proteins/metabolism , Sulfuric Acids/metabolismSubject(s)
Bile/metabolism , Swine/metabolism , Animals , Bicarbonates/metabolism , Bile Acids and Salts/metabolism , Carbon Radioisotopes , Common Bile Duct , Duodenum , Erythritol/blood , Erythritol/metabolism , Female , Hydrogen-Ion Concentration , Injections, Intravenous , Intubation , Methods , Osmolar Concentration , Potassium/metabolism , Sodium/metabolism , Taurocholic Acid/administration & dosage , Taurocholic Acid/pharmacologySubject(s)
Liver/physiology , Acid-Base Equilibrium , Animals , Bile Acids and Salts/analysis , Blood Flow Velocity , Blood Pressure , Blood Proteins/analysis , Galactose , Hemoglobins/analysis , Hemolysis , Hepatic Artery/physiology , Humans , In Vitro Techniques , Liver Diseases/therapy , Liver Function Tests , Oxygen Consumption , Perfusion , Portal Vein/physiology , Sulfobromophthalein , Swine/physiologySubject(s)
Bile Ducts/metabolism , Bile/metabolism , Cholagogues and Choleretics , Vasopressins/pharmacology , Animals , Bicarbonates/analysis , Bile/analysis , Bile Acids and Salts/metabolism , Bile Ducts, Intrahepatic/metabolism , Carbon Isotopes , Chlorides/analysis , Dogs , Erythritol/metabolism , Female , Potassium/analysis , Sodium/analysis , Taurocholic Acid/metabolismSubject(s)
Liver Diseases/therapy , Perfusion , Acid-Base Equilibrium , Animals , Bile/metabolism , Blood Circulation Time , Female , Galactose/metabolism , Hemodynamics , Hemolysis , Humans , Liver Circulation , Liver Cirrhosis/metabolism , Liver Function Tests , Male , Oxygen Consumption , Swine , Water-Electrolyte BalanceSubject(s)
Liver Diseases/therapy , Liver , Perfusion , Swine , Animals , Hepatic Encephalopathy/therapy , Humans , Liver/metabolism , Liver/physiology , Methods , Therapeutic IrrigationABSTRACT
Haemorrhagic hypotension (HH) causes a redistribution of intrarenal blood flow characterized by a patchy cortical hypoperfusion. Previous studies indicated that the sYmpathoadrenergic system is mainly responsible for these redistribution processes. The relative role of renal nerves and of circulating catecholamines was studied in the present experiments. Intrarenal haemodynamics were analysed by means of the 133 Xenon washout technique and 83 Krypton autoradiographics. 8 autotransplanted (and, therefore, chronically denervated) kidneys showed the same typical response to severe and prolonged HH as 11 normal control organs. In 2 additional dogs, the intrarenal distribution of blood flow (IDBF) and local blood flow rates (Fi ) of an acutely denervated kidney before and during HH did not show any differences as compared with the contralateral control organ. It is concluded that the patchy cortical hypoperfusion observed in the dog during severe haemorrhagic hypotension does not depend on an intact innervation of the kidney, but that it is mainly mediated by circulating catecholamines.