RESUMO
Glucagonoma is an endocrine tumor of almost exclusively pancreatic origin which is rarely associated with a clinical syndrome mainly characterized by migratory necrolytic erythema, hyperglycemia, weight loss, hypoaminoacidemia and anemia. Ten to 30% of the patients may present thromboembolic phenomenon, deep vein thrombosis and pulmonary embolism which often lead to the death of the patient. We report the case of a patient diagnosed with pancreatic glucagonoma the presentation of which consisted in episodes of repeated deep vein thrombosis without associated migratory necrolytic erythema.
Assuntos
Glucagonoma/complicações , Neoplasias Pancreáticas/complicações , Flebite/complicações , Idoso , Glucagonoma/patologia , Humanos , Masculino , Neoplasias Pancreáticas/patologia , Flebite/patologiaRESUMO
Langerhans cells granulomatosis is a rare disease characterized by the clonal proliferation of the Langerhans cell, a cell element pertaining to the mononuclear phagocytes system. Hepatic involvement may be presented, particularly in the multifocal or disseminated form, together with the remaining surrounding organs. Radiologic findings have recently been reported including echographic, computerized tomography and magnetic resonance of the hepatic lesion of the disease. The case of a patient whose initial radiographic study suggested the existence of hepatic metastasis and which was later diagnosed with multifocal granulomatosis of Langerhans cells with hepatic involvement is reported. Radiologic and histologic images are provided and the data reported in the literature concerning this disease are reviewed.
Assuntos
Histiocitose de Células de Langerhans/diagnóstico , Hepatopatias/diagnóstico , Neoplasias Hepáticas/diagnóstico , Adulto , Biópsia , Diagnóstico Diferencial , Histiocitose de Células de Langerhans/patologia , Humanos , Fígado/patologia , Hepatopatias/patologia , Imageamento por Ressonância Magnética , Masculino , Tomografia Computadorizada por Raios XAssuntos
Carcinoma de Células em Anel de Sinete/diagnóstico , Quilotórax/diagnóstico , Ascite Quilosa/diagnóstico , Neoplasias Gástricas/diagnóstico , Idoso , Carcinoma de Células em Anel de Sinete/complicações , Quilotórax/etiologia , Ascite Quilosa/etiologia , Humanos , Masculino , Neoplasias Gástricas/complicaçõesRESUMO
Sarcoidosis is a systemic granulomatous disease of unknown etiology which may present multiple clinical manifestations. Liver involvement is observed among 21-79% of the cases. Nonetheless, hepatic sarcoidosis is usually asymptomatic and the finding of cholestasis is an infrequent complication. In the last few years, the presence of multiple hypodense nodules in the liver and spleen has been described in 5-15% of these patients following the application of dynamic intravenous techniques in abdominal CT scan. Although the histopathologic study of these nodules suggests that their formation is due to the coalescence of the microscopic granulomas, the cause of this aggregation remains unknown. A case of hepatic sarcoidosis presenting chronic cholestasis and whose abdominal tomographic study with intravenous contrast demonstrated the existence of hypodense lesions in the liver and spleen suggesting malignant disseminated disease is reported.
Assuntos
Colestase Intra-Hepática/complicações , Hepatopatias/complicações , Sarcoidose/complicações , Esplenopatias/complicações , Adulto , Colestase Intra-Hepática/diagnóstico por imagem , Feminino , Humanos , Hepatopatias/diagnóstico por imagem , Sarcoidose/diagnóstico por imagem , Esplenopatias/diagnóstico por imagem , Tomografia Computadorizada por Raios XAssuntos
Músculos Abdominais , Abscesso/etiologia , Doença de Crohn/complicações , Adulto , Humanos , MasculinoRESUMO
BACKGROUND: The epidemiology of primary biliary cirrhosis (PBC) in Spain is still poorly known. In fact, remarkable differences between areas have been found. METHODS: The epidemiology of PBC was investigated in the South area of the city and the province of Granada from 1976 through 1989. Several clinical and epidemiological data were collected from 25 patients who met the criteria for PBC and the yearly incidence and prevalence were calculated. RESULTS: The ages of patients which PBC ranged from 31 to 74 years (mean age 50 +/- 10.5); 88% were females and 28% were diagnosed in the asymptomatic phase of the disease. The incidence for the study period was variable, with a maximum of 6.8 cases/million and an overall yearly incidence rate of 4.1 +/- 2.3 cases/million (7.1 +/- 4.3 cases/million for females). When the risk population was considered (people over 25 years) the respective values were 11.5 and 6.9 +/- 3.7 cases/million (12.1 +/- 7.2 cases/million for females). The prevalence showed a progressive increase, being 36.4 cases/million at the end of the study; for the "risk" population it was 61.5/million (100 cases/million for females). CONCLUSIONS: Incidence and prevalence of PBC in the area of study are within medium and medium-high values for Spain and Europe. As in other studies, personal environmental or social factors with epidemiological significance were not identified.