RESUMO
Liver tissues from 17 patients with advanced stages of beta-thal/Hb E disease were examined by light and electron microscopy, with emphasis on cellular damage due to excess iron overload. Various histochemical stains were performed to grade degrees of iron deposition and fibrosis, and to demonstrate hepatitis B surface antigen, in Kupffer cells as well as macrophages. The results of light and electron microscopic studies were correlated. There was a variation in the distribution of hepatic iron and the severity of fibrosis. In most of the cases ballooning degeneration of the hepatocytes, increase in number of lysosomes, hemosiderin and ferritin in hepatocytes as well as in the sinusoidal lining cells were found. The ferro-acidophilic body, representing another important form of hepatocellular necrosis also occurred. So far no precise mechanisms can be concluded.
Assuntos
Adolescente , Adulto , Biópsia , Feminino , Ferritinas/química , Hemoglobina E , Hemoglobinopatias/complicações , Hemossiderose/epidemiologia , Antígenos de Superfície da Hepatite B/química , Hospitais Universitários , Humanos , Hiperplasia , Hipertrofia , Células de Kupffer/patologia , Cirrose Hepática/epidemiologia , Lisossomos/química , Macrófagos/patologia , Masculino , Microscopia Eletrônica , Pessoa de Meia-Idade , Índice de Gravidade de Doença , Tailândia/epidemiologia , Talassemia beta/complicaçõesRESUMO
Glycogen storage disease type IV is rare. The disease is characterized by widespread storage of a polysaccharide similar to amylopectin. An autopsy case of a 6-year-old Thai boy with cirrhosis and deposits in the liver, heart, muscle and central nervous system was described along with histochemical and electron microscopic findings.
Assuntos
Criança , Doença de Depósito de Glicogênio/patologia , Doença de Depósito de Glicogênio Tipo IV/patologia , Humanos , Fígado/patologia , Masculino , Microscopia Eletrônica , Músculos/patologia , Miocárdio/patologia , TailândiaAssuntos
Biópsia , Criança , Consanguinidade , Feminino , Doença de Gilbert/sangue , Humanos , Testes de Função Hepática , LinhagemAssuntos
Adulto , Cesárea , Feminino , Humanos , Recém-Nascido , Cistos Ovarianos/patologia , Ovário/patologia , Gravidez , Complicações na Gravidez/patologiaRESUMO
An electron microscopic study was carried out on eleven surgical liver biopsy specimens obtained from patients with cholangiocarcinoma associated with opisthorchiasis. The tumor cells of histologically well differentiated cholangiocarcinoma had few cytoplasmic organelles. They contained relatively large nuclei, abundant free ribosomes and numerous groups of fine fibrils. Each cell was surrounded by a basement membrane. Numerous long microvilli were seen projecting into the glandular lumen. The moderately differentiated cholangiocarcinomatous cells exhibited increased organelle content, marked variation in the shape of the nuclei with deep cytoplasmic invagination into the nuclear membrane; there were small intranuclear pseudoinclusions, and shorter microvilli. The tumor cells showed intracellular microvillus-lined spaces, abundant free ribosomes, many fine fibrils and their surrounding basement membranes were incomplete. The ultrastructure of the poorly differentiated cholangiocarcinoma was similar to that of the moderately differentiated tumor, except for fewer microvilli, abundant cytoplasmic organelles, and ill-defined or absent basement membrane.