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1.
Rev Esp Enferm Dig ; 113(4): 300-301, 2021 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-33222478

RESUMEN

We present the case of a 58-year-old female with no relevant medical or surgical history, who was referred to our hospital with a solitary hepatic lesion. She presented a slightly abnormal liver function in a routine blood test: ALT 71 U/l (range 0-33), AST 40 U/l (range 0-32) and GGT 71 U/l (range 0-40), with no symptoms. Ultrasound imaging showed a 3-cm-size focal lesion with a peripheral hypoechoic rim in the right hepatic lobe. Abdominal computed tomography (CT) scan after contrast injection revealed a subcapsular hypodense lesion in segment VII with capsular retraction. Other extrahepatic lesions were not seen.


Asunto(s)
Hemangioendotelioma Epitelioide , Neoplasias Hepáticas , Neoplasias Vasculares , Femenino , Hemangioendotelioma Epitelioide/diagnóstico por imagen , Humanos , Neoplasias Hepáticas/diagnóstico por imagen , Persona de Mediana Edad , Tomografía Computarizada por Rayos X , Ultrasonografía
2.
Microbiome ; 7(1): 100, 2019 07 04.
Artículo en Inglés | MEDLINE | ID: mdl-31272480

RESUMEN

BACKGROUND: The microbial populations of the human intestinal tract and their relationship to specific diseases have been extensively studied during the last decade. However, the characterization of the human bile microbiota as a whole has been hampered by difficulties in accessing biological samples and the lack of adequate methodologies to assess molecular studies. Although a few reports have described the biliary microbiota in some hepatobiliary diseases, the bile microbiota of healthy individuals has not been described. With this in mind, the goal of the present study was to generate fundamental knowledge on the composition and activity of the human bile microbiota, as well as establishing its potential relationship with human bile-related disorders. RESULTS: Human bile samples from the gallbladder of individuals from a control group, without any record of hepatobiliary disorder, were obtained from liver donors during liver transplantation surgery. A bile DNA extraction method was optimized together with a quantitative PCR (qPCR) assay for determining the bacterial load. This allows the selection of samples to perform functional metagenomic analysis. Bile samples from the gallbladder of individuals suffering from lithiasis were collected during gallbladder resection and the microbial profiles assessed, using a 16S rRNA gene-based sequencing analysis, and compared with those of the control group. Additionally, the metabolic profile of the samples was analyzed by nuclear magnetic resonance (NMR). We detected, for the first time, bacterial communities in gallbladder samples of individuals without any hepatobiliary pathology. In the biliary microecosystem, the main bacterial phyla were represented by Firmicutes, Bacteroidetes, Actinobacteria, and Proteobacteria. Significant differences in the relative abundance of different taxa of both groups were found. Sequences belonging to the family Propionibacteriaceae were more abundant in bile samples from control subjects; meanwhile, in patients with cholelithiasis members of the families Bacteroidaceae, Prevotellaceae, Porphyromonadaceae, and Veillonellaceae were more frequently detected. Furthermore, the metabolomics analysis showed that the two study groups have different metabolic profiles. CONCLUSIONS: Our results indicate that the gallbladder of human individuals, without diagnosed hepatobiliary pathology, harbors a microbial ecosystem that is described for the first time in this study. Its bacterial representatives and metabolites are different from those detected in people suffering from cholelithiasis. In this regard, since liver donors have been subjected to the specific conditions of the hospital's intensive care unit, including an antibiotic treatment, we must be cautious in stating that their bile samples contain a physiologically normal biliary microbiome. In any case, our results open up new possibilities to discover bacterial functions in a microbial ecosystem that has not previously been explored.


Asunto(s)
Bilis/metabolismo , Bilis/microbiología , Vesícula Biliar/microbiología , Vesícula Biliar/fisiología , Microbiota , Adulto , Anciano , Bacterias/clasificación , Femenino , Humanos , Litiasis/microbiología , Masculino , Metabolómica , Metagenoma , Persona de Mediana Edad , ARN Ribosómico 16S/genética , ARN Ribosómico 18S/genética
3.
Rev Esp Enferm Dig ; 110(10): 678-679, 2018 10.
Artículo en Inglés | MEDLINE | ID: mdl-30286605

RESUMEN

We present the case of a patient with obstructive jaundice due to a polylobulated lesion at the middle common bile duct that is identified as a villous adenoma of the main bile duct. This entity is infrequent with few references in the bibliography. It is a benign pathology but with risk of malignancy, so the diagnosis and resection is essential for adequate treatment.


Asunto(s)
Adenoma Velloso , Neoplasias del Conducto Colédoco , Adenoma Velloso/diagnóstico , Adenoma Velloso/cirugía , Neoplasias del Conducto Colédoco/diagnóstico , Neoplasias del Conducto Colédoco/cirugía , Humanos
4.
Rev. esp. enferm. dig ; 110(10): 667-668, oct. 2018. ilus, tab
Artículo en Español | IBECS | ID: ibc-177823

RESUMEN

Presentamos el caso de una paciente de 29 años que consultó por rectorragias autolimitadas que fue diagnosticada de síndrome de Abernethy (shunt portosistémico congénito). Se trata de un debut clínico poco habitual en este tipo de síndrome congénito muy poco prevalente. La gran mayoría de los casos descritos en la literatura se manifiestan clínicamente en la edad pediátrica


We report the case of a 29-year-old patient who presented with a short history of lower gastrointestinal bleeding. A diagnosis of Abernethy syndrome was made (congenital extrahepatic portosystemic shunt) after this uncommon clinical presentation. The prevalence of this congenital malformation is very low and usually manifests during the pediatric age, according to previously published reports


Asunto(s)
Humanos , Femenino , Adulto , Hemangioma/diagnóstico por imagen , Encefalopatía Hepática/diagnóstico por imagen , Hemorragia Gastrointestinal/etiología , Endoscopía Gastrointestinal/métodos
6.
Rev Esp Enferm Dig ; 110(10): 667-668, 2018 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-30062901

RESUMEN

We report the case of a 29-year-old patient who presented with a short history of lower gastrointestinal bleeding. A diagnosis of Abernethy syndrome was made (congenital extrahepatic portosystemic shunt) after this uncommon clinical presentation. The prevalence of this congenital malformation is very low and usually manifests during the pediatric age, according to previously published reports.


Asunto(s)
Vena Porta/anomalías , Malformaciones Vasculares/diagnóstico , Adulto , Femenino , Hemorragia Gastrointestinal/etiología , Humanos , Síndrome , Malformaciones Vasculares/complicaciones
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