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3.
Med. infant ; 15(4): 312-319, dic. 2008. graf, tab
Article in Spanish | LILACS, BINACIS, UNISALUD | ID: lil-541260

ABSTRACT

El servicio de Emergentología del Hospital del Niño Jesús de Tucumán realizó un trabajo retrospectivo, que abarcó de Enero de 2005 hasta Abril de 2006, sobre menores de 14 años ingresados con diagnóstico de abuso sexual (AS). Se registraron 32 pacientes, de los cuales sólo 23 cumplieron con los criterios de inclusión. Las niñas fueron las más afectadas; los varones agredidos fueron en su mayoría menores de 5 años. El grupo más comprometido estuvo entre los 5 y 10 años. Casi el 80 por ciento de loa gredidos tenia menos de 10 años. Las familias de las victimas en 3/4 partes de los casos, eran disfuncionales, con necesidades básicas insatisfechas, y caracterizadas por alcoholismo en más de la mitad de los casos, violencia intrafamiiar y abandono paterno. Sin embargo, casi la cuarta parte de las agresiones se dio en hogares considerados bien constituidos. En casi todos los ataques el agresor era una persona conocida, la mayoría familiar directo, generalmente conviviente o vecino, que gozaba de la confianza de los niños y sus padres. Gran parte de las agresiones fueron reiteradas. La mayoría de los abusadores era mayor de edad ; el 41 por ciento tenía menos de 18 años y en dos casos, menos de 12 años. No hubo violencia o maltrato físico en más del 90 por ciento. Otro dato relevante fue la normalidad del examen físico en el 35 por ciento de los casos en los que el contacto se limitó a frotamientos, manoseos, estimulación oral o maniobras masturbatorias. Se deduce por lo tanto que un examen físico negativo no descarta AS. Se observó también alta incidencia de lesiones genitales y/o anales consideradas crónicas, como consecuencia de AS de larga data. El examen paricial sólo fue positivo en un 33 por ciento. Sin embargo, debe señalarse que las posibilidades de encontrar evidencia forense aumentan cuando la pericia se hace precozmente, antes de las 12 horas del hecho y cuando no se ha realizado antes del estudio el aseo genital.


Subject(s)
Infant, Newborn , Infant , Child, Preschool , Child , Adolescent , Child Abuse, Sexual , Informed Consent , Risk Factors , Pediatrics , Rape , Domestic Violence , Epidemiology, Descriptive , Retrospective Studies
4.
J Thromb Haemost ; 3(2): 216-20, 2005 Feb.
Article in English | MEDLINE | ID: mdl-15670021

ABSTRACT

Despite widespread use of laparoscopic procedures, no adequate data are available to support specific recommendations for venous thromboprophylaxis in patients undergoing laparoscopic surgery. This prospective, randomized trial is the first to be designed to evaluate a regimen of out-of-hospital thromboprophylaxis after laparoscopic surgery. Consecutive patients admitted for laparoscopic surgery were considered for the study. The thromboprophylaxis regimen used for each patient was based on a risk score. Possible thromboprophylactic measures included elastic stockings and pre- and postoperative Dalteparin or early ambulation. At discharge, patients were randomly allocated either to continue Dalteparin for 1 week, or to receive no further prophylaxis. Patients judged to be at low risk were not randomized. Compression ultrasound of the leg veins was performed in all patients 4 weeks after hospital discharge. Fifty-three patients, all with acute appendicitis, were judged to be at low risk of deep vein thrombosis and were not included in the randomized study. The remaining 209 patients fell into two groups: 104 patients received postdischarge Dalteparin and 105 patients did not. The incidence of deep vein thrombosis was 0% (0 of 104) vs. 0.95% (one of 105), respectively (P = 1.00). The risk of postdischarge venous thromboembolism is low in patients undergoing laparoscopic surgery who receive in-hospital thromboprophylaxis. Given this low risk, a clinical trial powered to determine if extending prophylaxis in such patients reduces the risk of clinically apparent deep vein thrombosis would be unfeasibly large.


Subject(s)
Fibrinolytic Agents/therapeutic use , Laparoscopy/adverse effects , Premedication , Thrombosis/prevention & control , Adult , Aged , Cohort Studies , Dalteparin/administration & dosage , Female , Humans , Male , Middle Aged , Perioperative Care , Risk Assessment , Thrombosis/drug therapy , Treatment Outcome
7.
Ann Ital Med Int ; 14(1): 46-50, 1999.
Article in Italian | MEDLINE | ID: mdl-10528424

ABSTRACT

Activated partial thromboplastin time may be prolonged as the result of either of two different autoimmune complications of chronic lymphocytic leukemia: the development of antiphospholipid antibodies, such as lupus anticoagulant or anticardiolipin antibodies, or anti-factor VIII inhibitors, such as acquired hemophilia A. In the rare simultaneous occurrence of both inhibitors, differential diagnosis of a prolonged activated partial thromboplastin time poses a number of problems during laboratory work-up, due to mutual interference of the commonly performed tests. Only careful clinical follow-up can disclose the significance of the laboratory findings. We report the case of concurrent antiphospholipid antibodies (lupus anticoagulant positivity, anticardiolipin antibodies; IgM 3880 MPL/mL and IgG 265 GPL/mL) and anti-factor VIII antibodies (46.8 Bethesda Units) in a patient with chronic B-cell lymphocytic leukemia who had prolonged activated partial thromboplastin time (78.8 s). The relationship between lymphoproliferative and antiphospholipid syndrome, laboratory work-up in the case of the association of antiphospholipid and anti-factor VIII antibodies, and related problems that occur during clinical management of the patient are also discussed.


Subject(s)
Antibodies, Antiphospholipid/blood , Antiphospholipid Syndrome/diagnosis , Factor VIII/immunology , Leukemia, Lymphocytic, Chronic, B-Cell/immunology , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Antiphospholipid Syndrome/etiology , Cyclophosphamide/administration & dosage , Doxorubicin/administration & dosage , Fatal Outcome , Female , Humans , Leukemia, Lymphocytic, Chronic, B-Cell/complications , Leukemia, Lymphocytic, Chronic, B-Cell/drug therapy , Middle Aged , Partial Thromboplastin Time , Prednisone/administration & dosage , Vincristine/administration & dosage
8.
J Ultrasound Med ; 18(9): 633-8, 1999 Sep.
Article in English | MEDLINE | ID: mdl-10478972

ABSTRACT

The aim of our study was to assess whether acute variations in portal vein Doppler sonographic parameters induced by administration of a single beta-blocker agent are predictive of the long-term effects of these drugs in the prevention of a first episode of variceal bleeding. In 30 patients with liver cirrhosis at high risk for variceal bleeding, duplex Doppler sonographic parameters (maximal portal flow velocity, portal blood flow, and congestion index) were measured before and 4 h after the administration of 40 mg of propranolol. Twenty-three of these patients started chronic therapy with propanolol and were evaluated periodically (seven patients were excluded because they did not continue the therapy). The percentage of patients free from bleeding was 86.9% at the first year and 77.8% at the second year. Among a series of clinical, laboratory, and instrument-based parameters, the only one related to first bleeding, selected by the Cox regression model, was the percentage decrease in maximal portal flow velocity observed after initial administration of propranolol (P < 0.01). The best cutoff value for the percentage decrease in portal flow velocity (portal flow velocity test) was 12%. The prevalence of bleeding had been 25% (3 of 12) in patients with positive portal flow velocity test results (12% decrease or more), versus 64% (7 of 11) in patients with negative portal flow velocity test results. The actuarial probability of remaining free from bleeding (Kaplan-Meier analysis) was different in these two groups (log rank P < 0.01). The portal flow velocity test represents a safe and feasible method to predict the efficacy of beta-blockers in the prevention of a first bleeding episode in patients with cirrhosis. In patients with negative results on the portal flow velocity test, an alternative therapeutic approach should be considered.


Subject(s)
Adrenergic beta-Antagonists/therapeutic use , Esophageal and Gastric Varices/prevention & control , Gastrointestinal Hemorrhage/prevention & control , Propranolol/therapeutic use , Ultrasonography, Doppler, Duplex , Actuarial Analysis , Blood Flow Velocity/drug effects , Esophageal and Gastric Varices/diagnostic imaging , Feasibility Studies , Female , Follow-Up Studies , Forecasting , Gastrointestinal Hemorrhage/diagnostic imaging , Humans , Liver Cirrhosis/diagnostic imaging , Liver Cirrhosis/drug therapy , Longitudinal Studies , Male , Middle Aged , Portal Vein/diagnostic imaging , Portal Vein/drug effects , Prevalence , Prognosis , Proportional Hazards Models , ROC Curve , Regional Blood Flow/drug effects , Safety
9.
Recenti Prog Med ; 89(6): 301-3, 1998 Jun.
Article in Italian | MEDLINE | ID: mdl-9658897

ABSTRACT

A case of massive upper gastrointestinal haemorrhage from proximal esophageal varices is reported. Upper esophageal varices occur rarely, and serve as collaterals in conditions of superior vena cava obstruction. In our patient, cervical esophageal varices were associated with portal hypertension due to occult liver cirrhosis. As the diagnosis was made at autopsy, this case serves to stress the importance of a through examination of the cervical portion of the esophagus during routine endoscopy.


Subject(s)
Esophageal and Gastric Varices/complications , Gastrointestinal Hemorrhage/etiology , Aged , Aged, 80 and over , Autopsy , Esophageal and Gastric Varices/diagnosis , Esophageal and Gastric Varices/pathology , Esophagus/pathology , Female , Hematemesis/etiology , Humans , Liver/pathology , Liver Cirrhosis/complications , Liver Cirrhosis/pathology , Melena/etiology , Spleen/pathology
10.
Minerva Cardioangiol ; 45(7-8): 335-47, 1997.
Article in Italian | MEDLINE | ID: mdl-9463169

ABSTRACT

BACKGROUND AND AIM: The capacity of the results of clinical studies to lead to changes in clinical practice is controversial. The treatment of elderly patients with acute myocardial infarction (AMI) represents an increasingly important challenge for the physician. The decreasing mortality rate for AMI in the general population is countered by an increasingly high mortality rate among the elderly. The aim of this prospective study was to evaluate the impact of the results of clinical studies on the treatment of AMI in community hospitals, and to highlight any differences in treatment and prognosis depending on age. MATERIALS AND METHODS: 123 patients with AMI were divided into two groups: (1) young patients (61.2%) aged under 75 (76 patients of whom 64 were male, with a mean age of 61.08 +/- 9.63) and (2) elderly patients (38.8%) aged over 75 (47 patients of whom 26 were male, with a mean age of 81.77 +/- 3.94). All patients were monitored for at least 12 months after discharge. RESULTS: The percentage administration of fibrinolytics (60.5%), aspirin (80.3%), beta-blockers (oral 40.8%; i.v. 32.9%) and anticoagulants (97.4%) showed that young patients were treated according to the indications reported in the literature. Thrombolysis was more frequently performed in young patients than in the aged (60.5% vs 10.6%; p = 0.0001). Multiple logistic regression analysis showed that age, Killip's class and time at hospitalization were variables predicting the exclusion from fibrinolysis. During hospitalization the elderly group received oral beta-blockers less frequently (8.5% vs 40.8%; p = 0.0001); on discharge, they less frequently received ACE-inhibitors (14.9% vs 46.1%; p = 0.0004), aspirin (48.9% vs 77.6%; p = 0.001), beta-blockers (12.8% vs 44.7%; p = 0.0002). The elderly group revealed a higher mortality rate both during hospitalization (19.1% vs 3.9%; p = 0.01) and follow-up (44.7% vs 11.0%; p = 0.0001). Multivariate analysis showed a direct correlation between ventricular arrhythmia and Killip's class and hospital mortality, whereas smoking and time at hospitalization were inversely correlated. Mortality during follow-up was directly associated with Killip's class and inversely to the use of ACE-inhibitors during hospitalization, and beta-blockers and diuretics on discharge. Kaplan-Meier analysis did not show any differences in the survival rate of the two groups, but the first year after AMI was particularly critical for elderly patients among whom 40% of all deaths were recorded. CONCLUSIONS: This study confirms the application in clinical practice of the results of clinical studies also in community hospitals, and shows that elderly AMI patients are high-risk patients. The high mortality in the latter group is correlated to the fact that they are less eligible to undergo fibrinolytic therapy and have a lower probability of receiving drugs of proven efficacy as a means of increasing survival after AMI. Further clinical studies are required to reduce mortality after AMI in a population that is increasingly widely represented in community hospitals.


Subject(s)
Myocardial Infarction/drug therapy , Adrenergic beta-Antagonists/therapeutic use , Adult , Aged , Aged, 80 and over , Angiotensin-Converting Enzyme Inhibitors/therapeutic use , Female , Hospitals, Community , Humans , Italy/epidemiology , Male , Middle Aged , Monitoring, Physiologic , Myocardial Infarction/epidemiology , Prospective Studies
11.
Clin Radiol ; 52(3): 220-3, 1997 Mar.
Article in English | MEDLINE | ID: mdl-9091257

ABSTRACT

AIM AND METHODS: This prospective study was carried on 20 patients (10 with liver cirrhosis and 10 with myelo-lymphoproliferative disorders), consecutively admitted to our ward for splenomegaly and thrombocytopenia, with the aim of evaluating the ability of Duplex-Doppler ultrasonography (DDUS) to discriminate between congestive splenomegaly and enlarged spleen caused by haematological disorders. RESULTS: Comparing the clinical/laboratory and DDUS findings for the two groups, it emerged that maximum-portal flow velocity (PFV) values revealed the most statistically significant differences: 17.31 SD 2.48 vs. 28.27 SD 3.53 (cm/s, P < 0.001). Discriminant analysis showed that max-PFV is the variable which by itself maximizes the separation between the two groups (F = 71.56; P < 0.0001). The patients with congestive splenomegaly exhibited lower max-PFV than the controls (17.31 SD 2.48 vs. 26.29 SD 2.38 cm/s, P < 0.001), unlike those with haematological diseases, whose max-PFV values were greater, albeit not significantly so (28.27 SD 3.53 vs. 26.29 SD 2.38 cm/s, P = 0.161). CONCLUSIONS: DDUS assessment of portal haemodynamics thus proved useful in the differential diagnosis of splenomegaly in asymptomatic patients since it distinguishes rapidly and non-invasively between congestive and haemotological splenomegaly. A lower-than-normal max-PFV value indicates congestive splenomegaly; a highish value, on the other hand, suggests a splenomegaly of haematological origin.


Subject(s)
Portal Vein/diagnostic imaging , Splenomegaly/diagnostic imaging , Splenomegaly/etiology , Ultrasonography, Doppler, Duplex , Adult , Blood Flow Velocity , Diagnosis, Differential , Female , Hematologic Diseases/complications , Hematologic Diseases/diagnostic imaging , Humans , Liver Cirrhosis/complications , Liver Cirrhosis/diagnostic imaging , Male , Middle Aged , Prospective Studies
12.
Recenti Prog Med ; 87(12): 586-8, 1996 Dec.
Article in Italian | MEDLINE | ID: mdl-9102696

ABSTRACT

211 patients were submitted to percutaneous ultrasound-guided liver biopsy: 184 patients (87.2%) had only one focal lesion, the other 27 had two or more lesions. In 9 patients (4.27%) the material drawn out from the liver was not adequate for microscopic examination (Retrieval Rate 95.7%). Histological evaluation revealed: absence of neoplasm in 67 patients (31.75%), benign lesion in 29 patients (13.74%), primitive malignant lesion in 70 patients (33.18%) and metastatic malignant lesion in 36 patients (17.06%). Combining the histological data with disease manifestation, biopsy showed a sensitivity of 95.1%, specificity of 100%, positive predictive value of 100%, negative predictive value of 89.4% and a diagnostic accuracy of 92.4%. None of the most important complications described in literature was observed. Our study confirms that ultrasound guided biopsy is a procedure of high diagnostic value in patients with nodular liver lesions, advantageous for its simplicity, low cost and safety.


Subject(s)
Liver Neoplasms/pathology , Liver/pathology , Biopsy, Needle/methods , Diagnosis, Differential , Humans , Liver/diagnostic imaging , Liver Cirrhosis/diagnostic imaging , Liver Cirrhosis/pathology , Liver Neoplasms/diagnostic imaging , Sensitivity and Specificity , Ultrasonography
13.
Recenti Prog Med ; 87(4): 150-3, 1996 Apr.
Article in Italian | MEDLINE | ID: mdl-8643874

ABSTRACT

Spontaneous bacterial perionitis (SBP) is a relatively frequent complication of liver cirrhosis and is associated with a high mortality if not early recognized and immediately treated. The text-books of Medicine available in Italy suggest the use of traditional laboratory tests (gravity, total protein concentration, Rivalta's test) to whom add white blood cell count for the assessment of the nature transudative (not infected) or exudative (infected) of ascitic fluid; nevertheless, in every day clinical practice, the association between total protein concentration and type of ascitic fluid may be misleading with respect to the diagnosis of SPB. The aim of this retrospective study, undertaken on 86 patients with liver cirrhosis consecutively admitted and separated in two groups, one without and the other with PSB (white blood cell count > 500/mm3), was to identify criteria for diagnosis of PSB. The traditional laboratory tests were significantly different in the two groups but Rivalta's test. Yet, none of them showed a diagnostic measurement sufficient for the use in the diagnosis of PSB (positive predittive value: gravity 41%, Rivalta's test 36%, total protein concentration 40%). The results of this work show the traditional laboratory tests unable to define the nature of the ascitic fluid. For the diagnosis of PSB the only reliable parameter is the white blood cell count.


Subject(s)
Ascitic Fluid/chemistry , Liver Cirrhosis/complications , Peritonitis/etiology , Aged , Bacterial Infections/microbiology , Female , Humans , Leukocyte Count , Male , Middle Aged , Peritonitis/microbiology , Predictive Value of Tests , Proteins/analysis , Specific Gravity
14.
Liver ; 16(2): 84-7, 1996 Apr.
Article in English | MEDLINE | ID: mdl-8740839

ABSTRACT

Upper gastrointestinal bleeding is a leading cause of death in patients with liver cirrhosis. In most cases haemorrhage originates from oesophageal varices or from congestive gastropathy, and the evaluation of the bleeding risk is based on oesophagogastroduodenoscopic data. The aim of this prospective study was to determine whether the measurement of portal flow velocity by Duplex-Doppler, compared with endoscopic data, can help in detecting patients with cirrhosis at risk of bleeding. One hundred and seventy-three patients underwent endoscopy to ascertain the size of the varices and the severity of congestive gastropathy. For each patient maximal portal flow velocity measurements were obtained. No difference in portal flow velocity was observed between patients with or without oesophageal varices or congestive gastropathy. During a 2-year observation period, 27 patients (15.6%) had at least one episode of acute digestive bleeding. Stepwise multiple logistic regression analysis demonstrated a correlation between oesophageal varices and congestive gastropathy endoscopic grading and the incidence of bleeding; only the former was entered into the final regression equation (p < 0.001). No relationship between the max portal flow velocity value and incidence of bleeding was found. This study shows that portal flow velocity is unrelated to the degree of the endoscopic abnormalities in patients with liver cirrhosis and that it has no value in the identification of patients with cirrhosis at risk of upper gastrointestinal bleeding.


Subject(s)
Gastrointestinal Hemorrhage/etiology , Hypertension, Portal/complications , Liver Cirrhosis/complications , Adult , Aged , Blood Flow Velocity/physiology , Endoscopy, Digestive System , Esophageal and Gastric Varices/complications , Female , Gastrointestinal Hemorrhage/diagnosis , Humans , Liver Cirrhosis/physiopathology , Male , Middle Aged , Portal Vein/diagnostic imaging , Portal Vein/physiopathology , Prospective Studies , Risk , Stomach Diseases/complications , Ultrasonography, Doppler, Duplex
15.
Eur J Gastroenterol Hepatol ; 7(9): 893-7, 1995 Sep.
Article in English | MEDLINE | ID: mdl-8574724

ABSTRACT

BACKGROUND: Patients with liver cirrhosis and large oesophageal varices run a high risk of digestive haemorrhage due to the rupture of oesophageal varices, an event associated with a high mortality. At present, the only treatment for the prevention of first bleeding from oesophageal varices on which there is general agreement is drug-based. In order to tailor drug treatment to the requirements of individual patients more precisely, an ever-increasing number of drugs is being investigated. DESIGN: Double-blind cross-over study. METHODS: Sixteen cirrhotic patients with large oesophageal varices were studied by means of duplex-Doppler ultrasonography to determine variations in portal haemodynamics after oral administration of 0.150 mg clonidine and to compare these with the variations observed after oral administration of 40 mg propranolol. RESULTS: Propranolol caused a significant reduction in maximum portal flow velocity (P < 0.001), whereas clonidine failed to cause any such variation (P = 0.194). Considering as responders those patients who exhibited at least a 10% decrease in maximum portal flow velocity, 11 patients responded to propranolol; of these, three also responded to clonidine. No patient responded only to clonidine. CONCLUSION: The absence of any effects on the parameters of portal haemodynamics would appear to deny clonidine any significant role in preventing first bleeding resulting from the rupture of oesophageal varices.


Subject(s)
Adrenergic alpha-Agonists/pharmacology , Clonidine/pharmacology , Hypertension, Portal/physiopathology , Liver Cirrhosis/physiopathology , Portal System/drug effects , Propranolol/pharmacology , Sympatholytics/pharmacology , Administration, Oral , Blood Flow Velocity/drug effects , Blood Pressure/drug effects , Cross-Over Studies , Double-Blind Method , Esophageal and Gastric Varices/prevention & control , Female , Gastrointestinal Hemorrhage/prevention & control , Hemodynamics/drug effects , Humans , Hypertension, Portal/complications , Hypertension, Portal/drug therapy , Liver Cirrhosis/complications , Liver Cirrhosis/diagnostic imaging , Male , Middle Aged , Portal System/diagnostic imaging , Portal System/physiopathology , Ultrasonography, Doppler, Duplex
16.
Recenti Prog Med ; 85(11): 517-20, 1994 Nov.
Article in Italian | MEDLINE | ID: mdl-7855384

ABSTRACT

In about 50% of patients with liver cirrhosis, upper digestive bleeding is not due to oesaphageal varices rupture, but to a group of peculiar mucosal lesions usually referred as "congestive gastropathy" and "hepatogenic ulcer". The pathogenesis of such mucosal damage is still unclear: an important causative role is commonly thought to be played by portal hypertension, but the role of peptical pathway and of the mucosal barrier impairment must not be underscored as well. Aim of this study was to evaluate the effect of roxatidine in the long-term treatment of mucosal damage in 19 patients with liver cirrhosis. Patients showed a good tolerance and no side effects. The improvement of endoscopic pattern after a three months period of roxatidine therapy was statistically significant; moreover there was no occurrence of digestive bleeding. In conclusion, H2 antagonist may be considered as the drug of choice for the treatment of mucosal damage in patients with liver cirrhosis, for both its safety and effectiveness.


Subject(s)
Duodenal Diseases/drug therapy , Histamine H2 Antagonists/therapeutic use , Liver Cirrhosis/complications , Piperidines/therapeutic use , Stomach Diseases/drug therapy , Adult , Aged , Duodenal Diseases/etiology , Female , Gastric Mucosa , Humans , Intestinal Mucosa , Male , Middle Aged , Stomach Diseases/etiology
17.
Ital J Gastroenterol ; 26(6): 303-5, 1994.
Article in English | MEDLINE | ID: mdl-7524803

ABSTRACT

The case of a 70-year-old man with clinically-compensated alcoholic liver cirrhosis is illustrated. His serum alpha-fetoprotein level was on the increase but Ultrasonography and Magnetic Resonance detected no focal lesion of the liver. Five months after Ultrasonography, Computed Tomography and Magnetic Resonance were performed because the patient's alpha-fetoprotein level indicated hepatocellular carcinoma, but none of these tests succeeded in locating the neoplasm. Digital subtraction angiography was performed and only then was a small hepatocellular carcinoma revealed under the diaphragm. The patient underwent transcatheter arterial chemo-embolization with the result that the alpha-fetoprotein level dropped immediately and is still normal after 15 months. The case described is a model of what the ideal function of a marker of neoplasia should be, namely early detection, and subsequent precise confirmation of the continuing efficacy of the treatment adopted.


Subject(s)
Carcinoma, Hepatocellular/diagnosis , Liver Neoplasms/diagnosis , alpha-Fetoproteins/analysis , Aged , Angiography, Digital Subtraction , Carcinoma, Hepatocellular/diagnostic imaging , Carcinoma, Hepatocellular/therapy , Chemoembolization, Therapeutic , Humans , Liver Neoplasms/diagnostic imaging , Liver Neoplasms/therapy , Magnetic Resonance Imaging , Male , Tomography, X-Ray Computed
18.
Recenti Prog Med ; 85(4): 235-7, 1994 Apr.
Article in Italian | MEDLINE | ID: mdl-7517061

ABSTRACT

The cases of two patients with liver cirrhosis HCV-related, admitted in our Department in consequence of the development of ascites, anemia and clinical deterioration, are reported. Both patients had all major risk factors for hepatocellular carcinoma and anamnestic and physical findings suggesting this diagnosis; nevertheless, the alpha-1-fetoprotein serum levels and the ultrasonographic findings were not diagnostic for primary hepatic neoplasm. Explorative paracentesis was diagnostic, demonstrating the presence of hemoperitoneum (the hematocrit ratio in the ascitic fluid was 12 and 10, respectively). Magnetic resonance revealed extensive diffuse hepatocellular carcinoma on both cases. Hemoperitoneum, in patients with liver cirrhosis, in face of non diagnostic levels of alpha-1-fetoprotein and ultrasonographic findings, can be indicative of the spontaneous rupture of a diffuse type of hepatocellular carcinoma.


Subject(s)
Carcinoma, Hepatocellular/diagnosis , Hemoperitoneum/etiology , Liver Cirrhosis/complications , Liver Neoplasms/diagnosis , Carcinoma, Hepatocellular/complications , Carcinoma, Hepatocellular/diagnostic imaging , Hemoperitoneum/diagnosis , Humans , Liver Neoplasms/complications , Liver Neoplasms/diagnostic imaging , Magnetic Resonance Imaging , Male , Middle Aged , Punctures , Ultrasonography , alpha-Fetoproteins/analysis
19.
Clin Ter ; 143(4): 315-9, 1993 Oct.
Article in Italian | MEDLINE | ID: mdl-8258266

ABSTRACT

Twenty-five liver cirrhosis patients with endoscopically demonstrated gastro-duodenal mucosal damage (microhemorrhages, erosions, ulcers) were treated with misoprostol (prostaglandin E1) 400 mg/die. Eleven patients (44%) had abdominal pain and diarrhea and stopped treatment. Three months later, a new endoscopy was performed in the 11 patients that completed the study (3 patients were lost at follow up). Mucosal damage was stable in 5 patients (45%) and improved in 6 patients (55%), with complete absence of mucosal lesions in 2 patients (P = 0.027, Wilcoxon Ranks test). No case of worsening was observed and no patient had digestive bleeding during treatment. Digestive bleeding is a common complication of liver cirrhosis, originating in about 50% of cases from gastro-duodenal mucosal damage. Misoprostol suggests itself as a possible alternative therapy to the drugs usually utilized in these lesions (beta-blockers, H2-inhibitors), but individual intolerance is frequent and must be preliminary excluded.


Subject(s)
Duodenum/drug effects , Gastric Mucosa/drug effects , Intestinal Mucosa/drug effects , Liver Cirrhosis/drug therapy , Misoprostol/therapeutic use , Aged , Chronic Disease , Drug Evaluation , Duodenum/pathology , Endoscopy, Digestive System , Female , Gastric Mucosa/pathology , Humans , Intestinal Mucosa/pathology , Liver Cirrhosis/complications , Liver Cirrhosis/pathology , Male , Middle Aged
20.
J Ultrasound Med ; 12(9): 525-9, 1993 Sep.
Article in English | MEDLINE | ID: mdl-8107184

ABSTRACT

Eighteen cirrhotic patients with esophageal varices at risk for bleeding took part in a double-blind study. The variations in PFV induced by either 40 mg of propranolol or 60 mg of sustained-release isosorbide-5-mononitrate on two consecutive days were evaluated with a duplex Doppler device. Both drugs caused a significant decrease in maximum (propranolol, P = 0.002; isosorbide-5-mononitrate, P = 0.021). Four patients responded to propranolol, three to isosorbide-5-mononitrate, and eight to both drugs; three did not show any change. Duplex Doppler sonography may be of use in the selection of the right pharmacologic treatment for the individual patient for the prevention of a bleeding esophageal varix.


Subject(s)
Hypertension, Portal/drug therapy , Hypertension, Portal/physiopathology , Isosorbide Dinitrate/analogs & derivatives , Propranolol/therapeutic use , Delayed-Action Preparations , Double-Blind Method , Drug Monitoring , Esophageal and Gastric Varices/complications , Esophageal and Gastric Varices/etiology , Female , Gastrointestinal Hemorrhage/etiology , Hemodynamics/drug effects , Humans , Hypertension, Portal/diagnostic imaging , Isosorbide Dinitrate/therapeutic use , Liver Cirrhosis/complications , Male , Middle Aged , Splanchnic Circulation/drug effects , Ultrasonography
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