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2.
BJR Case Rep ; 5(3): 20190005, 2019 Sep.
Article in English | MEDLINE | ID: mdl-31555475

ABSTRACT

Hepatic artery thrombosis is the most frequent vascular complication following orthotopic liver transplantation, and often results in biliary complications, early graft loss and death. Surgical revascularization and retransplantation are considered the mainstay of treatment. However, intraarterial endovascular therapy is an alternative that has shown low morbidity and mortality, thereby avoiding the need for retransplantation. We describe a case of orthotopic liver transplantation complicated with hepatic artery thrombosis that was successfully treated with endovascular therapy.

3.
Rev. esp. enferm. dig ; 108(4): 228-230, abr. 2016. ilus
Article in English | IBECS | ID: ibc-151346

ABSTRACT

Gilbert’s syndrome is a benign condition characterized by asymptomatic sporadic episodes of jaundice, due to a mild unconjugated hyperbilirubinemia caused by a deficiency in bilirubin glucoronidation. Under certain physiologic or pathologic events, bilirubin level rises but according to literature it does not reach out more than 3 mg/dl. We report 2 cases of Gilbert’s syndrome, genetically tested, which presented with bilirubin levels above 6 mg/dl without any trigger or coexisting condition. In conclusion, bilirubin levels higher than 6 mg/dl in Gilbert syndrome are rare, hemolytic and other metabolism diseases must be ruled out, and enetic testing may be necessary in some cases (AU)


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Subject(s)
Humans , Male , Young Adult , Adult , Gilbert Disease/complications , Gilbert Disease/diagnosis , Gilbert Disease/genetics , Bilirubin/analysis , Jaundice/complications , Jaundice/diagnosis , Jaundice/genetics , Genetic Testing/methods , Genetic Testing , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Hyperbilirubinemia, Hereditary/diagnosis , Hyperbilirubinemia, Hereditary/genetics , Hyperbilirubinemia/complications , Hyperbilirubinemia/diagnosis , Hyperbilirubinemia/genetics
4.
Rev Esp Enferm Dig ; 108(4): 228-30, 2016 Apr.
Article in English | MEDLINE | ID: mdl-26181050

ABSTRACT

Gilbert's syndrome is a benign condition characterized by asymptomatic sporadic episodes of jaundice, due to a mild unconjugated hyperbilirubinemia caused by a deficiency in bilirubin glucoronidation. Under certain physiologic or pathologic events bilirubin level rises but according to literature it does not reach out more than 3 mg/dl. We report 2 cases of Gilbert's syndrome, genetically tested, which presented with bilirubin levels above 6 mg/dl without any trigger or coexisting condition. In conclusion, bilirubin levels higher than 6 mg/dL in Gilbert syndrome are rare, hemolytic and other metabolism diseases must be ruled out, and genetic testing may be necessary in some cases.


Subject(s)
Bilirubin/blood , Gilbert Disease/blood , Gilbert Disease/diagnosis , Hyperbilirubinemia/blood , Hyperbilirubinemia/diagnosis , Adolescent , Genetic Testing , Gilbert Disease/genetics , Humans , Hyperbilirubinemia/genetics , Male , Young Adult
5.
Adv Pharmacol Sci ; 2014: 373295, 2014.
Article in English | MEDLINE | ID: mdl-25505905

ABSTRACT

Following chronic liver injury, hepatocytes undergo apoptosis leading to activation of hepatic stellate cells (HSC). Consequently, activated HSC proliferate and produce excessive extracellular matrix, responsible for the scar formation. The pandemic trend of obesity, combined with the high incidence of alcohol intake and viral hepatitis infections, highlights the urgent need to find accessible antifibrotic therapies. Treatment strategies should take into account the versatility of its pathogenesis and act on all the cell lines involved to reduce liver fibrosis. Medicinal plants are achieving popularity as antifibrotic agents, supported by their safety, cost-effectiveness, and versatility. This review will describe the role of hepatocytes and HSC in the pathogenesis of liver fibrosis and detail the mechanisms of modulation of apoptosis of both cell lines by twelve known hepatoprotective plants in order to reduce liver fibrosis.

6.
Chin Med ; 9(1): 27, 2014.
Article in English | MEDLINE | ID: mdl-25606051

ABSTRACT

During chronic liver injury, hepatic stellate cells (HSC) are activated and proliferate, which causes excessive extracellular matrix (ECM) deposition, leading to scar formation and fibrosis. Medicinal plants are gaining popularity as antifibrotic agents, and are often safe, cost-effective, and versatile. This review aims to describe the protective role and mechanisms of medicinal plants in the inhibition of HSC activation and ECM deposition during the pathogenesis of liver fibrosis. A systematic literature review on the anti-fibrotic mechanisms of hepatoprotective plants was performed in PubMed, which yielded articles about twelve relevant plants. Many of these plants act via disruption of the transforming growth factor beta 1 signaling pathway, possibly through reduction in oxidative stress. This reduction could explain the inhibition of HSC activation and reduction in ECM deposition. Medicinal plants could be a source of anti-liver fibrosis compounds.

7.
Rev Invest Clin ; 63 Suppl 1: 73-8, 2011 Sep.
Article in Spanish | MEDLINE | ID: mdl-22916615

ABSTRACT

BACKGROUND: Liver transplantation is the only curative alternative for patients with end stage liver disease or acute liver failure. AIM: To report the experience of a single transplant center in Mexico. MATERIAL AND METHODS: Fifty-five transplants in 54 adult patients were analyzed between 1999 and 2011 in a single private institution. All grafts were obtained from deceased donor. Surgical technique, donor and recipient demographics, complications, causes of death and overall survival are described. Results were expressed as range and percentages. A Kaplan-Meier survival curve was done to analyze patient and graft survival. RESULTS: Main cause of cirrhosis was hepatitis C virus infection followed by alcohol intake. A 16% of patients developed biliary complications without graft loss, and vascular complications were observed in 15%. Patient survival at one and five years was 83% and 76%, respectively. CONCLUSIONS: Complication rates and survival in our center are comparable to those in the United States and Europe.


Subject(s)
Liver Transplantation/statistics & numerical data , Adolescent , Adult , Hospitals , Humans , Liver Transplantation/adverse effects , Mexico , Middle Aged , Postoperative Complications/epidemiology , Postoperative Complications/etiology , Retrospective Studies , Young Adult
9.
Transplantation ; 77(7): 1038-40, 2004 Apr 15.
Article in English | MEDLINE | ID: mdl-15087768

ABSTRACT

BACKGROUND: The high cost of cyclosporine A (CsA) is an impediment for low-income patients. Previous studies have used ketoconazole at doses between 200 and 400 mg/day to lower CsA consumption. METHODS: Ketoconazole and CsA were administered prospectively to renal transplant patients. Patients treated historically with CsA were used as a reference group. At different intervals posttransplant, clinical and laboratory data were recorded. RESULTS: The reference group (n=14) was treated with CsA from 1992 to 1997 and the CsA plus ketoconazole group (n=17) from 1998 to 2002. Follow-up was 76+/-22 and 29+/-14 months, respectively. CsA doses throughout the study were 4.0+/-1.3 and 1.6+/-0.6 mg/kg/day (a 60% reduction, P =0.00). Trough levels of CsA were 194+/-87 and 193+/-69 ng/mL, respectively. The ketoconazole dose was 54+/-17 mg/day. The monthly cost of CsA was reduced by 60%, including the cost of ketoconazole. CONCLUSIONS: CsA with ketoconazole resulted in a substantial dose and cost reduction that proved safe and effective.


Subject(s)
Antifungal Agents/therapeutic use , Cyclosporine/therapeutic use , Immunosuppressive Agents/therapeutic use , Ketoconazole/therapeutic use , Kidney Transplantation , Adult , Female , Humans , Male , Middle Aged
10.
Bol. méd. Hosp. Infant. Méx ; 48(3): 185-8, mar. 1991. ilus
Article in Spanish | LILACS | ID: lil-105100

ABSTRACT

Se presenta un caso de lipoblastoma benigno de mediastino en un niño de 14 años de edad atendido en el Hospital Universitario "Dr. José E. González", Monterrey, N.L. Esta patología es muy poco frecuente, sobre todo en esta edad y en esta localización. Se trata de un tumor benigno que requiere resección completa. Al paciente se le practicó una tocacotomía anterolateral bilateral resecando completamente el tumor, siendo su peso de 3,100 g y midiendo 26 por 21 cm. La evolución fué satisfactoria


Subject(s)
Mediastinal Neoplasms/diagnosis , Mediastinum/abnormalities , Adipose Tissue/pathology , Adipose Tissue/surgery , Mediastinal Neoplasms/physiopathology , Mediastinal Neoplasms/therapy , Mediastinum/pathology , Mediastinum/surgery
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