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ویرایش: 10
نویسندگان: Jay H. Lefkowitch MD
سری:
ISBN (شابک) : 0702075841, 9780702075841
ناشر: Elsevier
سال نشر: 2020
تعداد صفحات: 458
زبان: English
فرمت فایل : PDF (درصورت درخواست کاربر به PDF، EPUB یا AZW3 تبدیل می شود)
حجم فایل: 45 مگابایت
در صورت تبدیل فایل کتاب Scheuer's Liver Biopsy Interpretation به فرمت های PDF، EPUB، AZW3، MOBI و یا DJVU می توانید به پشتیبان اطلاع دهید تا فایل مورد نظر را تبدیل نمایند.
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تفسیر بیوپسی کبد Scheuer که بیش از 50 سال توسط آسیب شناسان در عمل و آموزش مورد اعتماد است، یک راهنمای سازمان یافته و فوق العاده مصور است که برای کمک به حل مشکلات تشخیصی در میکروسکوپ طراحی شده است. این متن عملی که توسط متخصص مشهور دکتر جی لفکوویچ نوشته شده و تجربه گسترده مرحوم دکتر پیتر شوئر را منعکس می کند، حاوی نکات فنی، سرنخ های تشخیصی و مروارید در مورد همه جنبه های تشخیص آسیب شناسی کبد، از جمله حاد است. و هپاتیت مزمن، بیماری های مجاری صفراوی، اختلالات دوران کودکی، و نئوپلاسم های کبدی - و همچنین موضوعات جانبی مانند ارزیابی بیوپسی، تکنیک های آزمایشگاهی، بافت شناسی طبیعی کبد و پیوند. در سرتاسر متن، ویژگیهای هیستوپاتولوژیک با ویژگیهای بالینی، ژنتیک مولکولی و ایمونوهیستوشیمی مرتبط است تا یک توضیح عملی از نحوه تأثیر آسیبشناسی بر تشخیص و مدیریت بیماری کبد ارائه شود.</ p>
Trusted for more than 50 years by pathologists in practice and in training, Scheuer’s Liver Biopsy Interpretation is a well-organized, superbly illustrated guide designed to help solve diagnostic problems at the microscope. Authored by renowned expert Dr. Jay Lefkowitch and reflecting the extensive experience of the late Dr. Peter Scheuer, this practical text contains technical tips, diagnostic clues, and pearls on all aspects of liver pathology diagnosis, including acute and chronic hepatitis, biliary tract diseases, childhood disorders, and hepatic neoplasms – as well as ancillary topics such as biopsy assessment, laboratory techniques, normal liver histology, and transplantation. Throughout the text, histopathologic features are correlated with clinical features, molecular genetics, and immunohistochemistry to provide a practical account of how pathology impacts the diagnosis and management of liver disease.
Cover Dedication SCHEUER’S Liver Biopsy Interpretation Copyright Preface Acknowledgements 1 - General Principles of Biopsy Assessment Introduction Type and adequacy of liver biopsy specimen The specimen at the bedside and in the laboratory References 2 - Laboratory Techniques Processing of the specimen Choice of stains References General reading 3 - The Normal Liver Structures and components Functional units and nomenclature Portal tracts Bile ducts Hepatic sinusoids, space of Disse and extracellular matrix Hepatic Sinusoids Space of Disse Hepatocytes Hepatocellular pigments Normal appearances in childhood Ageing Biopsy of the normal liver References General reading 4 - Assessment and Differential Diagnosis of Pathological Features Differential diagnosis of individual findings 5 - Biliary Disease Introduction Cholestasis Large bile-duct obstruction Chronic bile-duct obstruction and biliary cirrhosis Cholangitis: infection of the biliary tree Primary sclerosing cholangitis Primary biliary cholangitis (formerly primary biliary cirrhosis) The portal lesion of primary biliary cholangitis The progressive lesion of primary biliary cirrhosis Overlap syndromes, transitional diseases and autoimmune cholangitis Other disorders with intrahepatic bile-duct loss References General reading 6 - Acute Viral Hepatitis Introduction Pathological features Hepatocellular damage The inflammatory infiltrate Portal changes Histological variants Individual causes of viral hepatitis Hepatitis A Hepatitis B Hepatitis C Hepatitis D (delta hepatitis) Hepatitis E virus LBI-10 Differential diagnosis of acute viral hepatitis Fate and morphological sequelae of acute viral hepatitis Resolution Scarring Fatal outcome or need for liver transplantation Chronic hepatitis Cirrhosis Hepatocellular carcinoma References General reading 7 - Steatosis, Steatohepatitis and Related Conditions Steatosis Macrovesicular steatosis Microvesicular steatosis Alcoholic and non-alcoholic fatty liver disease Systematic histological approach to macrovesicular fatty liver disease Diabetes mellitus Steatohepatitis, alcoholic and non-alcoholic Pathological features of steatohepatitis Non-alcoholic steatohepatitis Histological differential diagnosis Other alcohol-related liver lesions Alcoholic foamy degeneration Fibrosis Fetal alcohol syndrome Cirrhosis Other lesions References General reading 8 - Drugs and Toxins Introduction Classification and mechanisms Commonly implicated and newer agents Morphological categories Adaptation Non-hepatitic liver-cell damage Hepatocellular necrosis Acute drug-induced hepatitis Differential diagnosis Chronic drug-induced hepatitis Differential diagnosis Steatohepatitis Fibrosis and cirrhosis Steroid-induced cholestasis Differential diagnosis Idiosyncratic drug-induced cholestasis Differential diagnosis Granulomas Other lesions References General reading 9 - Chronic Hepatitis Definition and causes Classification and nomenclature Use of liver biopsy in chronic hepatitis Histological features of chronic hepatitis Portal changes Parenchymal changes The periportal lesion: interface hepatitis The lobular lesion Individual causes of chronic hepatitis Chronic hepatitis B Chronic hepatitis D (with HBV) Chronic hepatitis C Pathological features Chronic hepatitis E Autoimmune hepatitis Other conditions with features of autoimmune hepatitis Differential diagnosis of chronic hepatitis Semi-quantitative scoring: grading and staging Interpretation of the results of scoring References General reading 10 - Cirrhosis Introduction Diagnosis of cirrhosis by liver biopsy Fragmentation Abnormal structure Hepatocellular changes Differential diagnosis Assessment of cause Pattern of nodules and fibrosis Bile ducts Blood vessels Steatohepatitis Evidence of viral infection Abnormal deposits Anatomical type Stage of development Histological activity Complications References General reading 11 - Neoplasms and Nodules Introduction Neoplasms and nodules in adults Benign lesions Hepatocellular adenoma Focal nodular hyperplasia Nodular regenerative hyperplasia Bile-duct adenoma Biliary cystadenoma Haemangioma Mesenchymal and neural tumours Inflammatory pseudotumour Malignant lesions Precursors of hepatocellular carcinoma Hepatocellular carcinoma Fibrolamellar carcinoma Bile-duct carcinoma (cholangiocarcinoma) Angiosarcoma Epithelioid haemangioendothelioma Extrahepatic malignancy and the liver Metastatic tumour Lymphomas and leukaemias Hodgkin’s disease Non-Hodgkin’s lymphoma and other haemopoietic malignancies Neoplasms and nodules in children Benign lesions Mesenchymal hamartoma Infantile haemangioendothelioma Malignant lesions Hepatoblastoma Sarcoma and lymphoma Hepatocellular carcinoma Cytopathological diagnosis Normal or reactive liver Cirrhosis and liver-cell dysplasia Hepatocellular adenoma Focal nodular hyperplasia Haemangioma Hepatocellular carcinoma Hepatoblastoma Cholangiocarcinoma Angiosarcoma Lymphoma Metastatic tumours References General reading 12 - Vascular Disorders The hepatic arteries Shock, heart failure and heatstroke The portal veins Portal hypertension The hepatic sinusoids Peliosis hepatis Disseminated intravascular coagulation Sickle-cell disease Venous congestion and outflow obstruction Cardiac failure and congestive hepatopathy Obstruction to large veins Sinusoidal obstruction syndrome/veno-occlusive disease References General reading 13 - Childhood Liver Disease and Metabolic Disorders Introduction Diagnostic approach to neonatal liver biopsy Neonatal hepatitis Extrahepatic biliary atresia Choledochal cyst Autoimmune sclerosing cholangitis Langerhans cell histiocytosis Paucity of intrahepatic bile ducts in childhood Fibropolycystic diseases Congenital hepatic fibrosis Caroli’s disease (congenital dilatation of the intrahepatic bile ducts) Microhamartoma Polycystic disease Inherited metabolic disorders Cystic fibrosis Storage disorders: general remarks Glycogen storage diseases (glycogenoses) Alpha1-antitrypsin deficiency Gaucher’s disease (glycosyl ceramide lipidosis) Niemann–Pick disease (sphingomyelin lipidosis) Wolman’s disease and cholesterol ester storage disease Galactosaemia Disorders of ureagenesis Reye’s syndrome Parenteral nutritions Hyperbilirubinaemias Inherited cholestatic syndromes Cirrhosis in childhood References General reading 14 - Disturbances of Copper and Iron Metabolism Wilson’s disease (hepatolenticular degeneration) Iron overload Siderosis Numerical assessment of tissue iron Primary iron overload disorders Classic HFE-related hereditary haemochromatosis Other primary iron overload disorders Secondary iron overload disorders Neonatal haemochromatosis Iron overload in haematological disorders Liver disease of varied aetiology References General reading 15 - The Liver in Systemic Disease and Pregnancy Introduction Granulomas Viral diseases Cytomegalovirus infection Infectious mononucleosis Acquired immune deficiency syndrome Drug-related hepatotoxicity Opportunistic infections and infestations AIDS cholangiopathy Peliosis hepatis Lymphomas Chronic hepatitis Steatosis and other changes Rickettsial, bacterial and fungal infections Q fever Brucellosis Typhoid fever Cat-scratch disease Tuberculosis Leprosy Spirochaetal infection Syphilis Leptospirosis Lyme disease Candidiasis Histoplasmosis The liver in sepsis Parasitic diseases Toxoplasmosis Malaria Visceral leishmaniasis (kala-azar) Amoebiasis Schistosomiasis Liver flukes Ascariasis Larval diseases Gastrointestinal disorders and the liver Chronic inflammatory bowel disease Haematological disorders and the liver Haemophilia Extramedullary haemopoiesis The liver in rheumatoid, immune-complex and collagen diseases Amyloidosis and light-chain deposition The liver in the porphyrias Non-specific reactive changes The liver in pregnancy Acute fatty liver of pregnancy Pre-eclampsia/eclampsia HELLP syndrome References Intrahepatic cholestasis of pregnancy General reading 16 - The Liver in Organ Transplantation Introduction Liver transplantation Assessment of the donor liver The liver allograft biopsy: general considerations Graft rejection Antibody-mediated (humoral) rejection Acute (cellular) rejection Chronic (ductopenic) rejection Other causes of graft dysfunction Infection Biliary obstruction Thrombosis Drug toxicity Immunosuppression withdrawal Recurrent disease De novo autoimmune hepatitis Neoplastic disease Late liver-allograft dysfunction Differential diagnosis in transplant biopsies Renal transplantation Bone marrow transplantation References General reading 17 - Electron Microscopy and Other Techniques Introduction Electron microscopy of liver biopsies The normal liver and examples of ultrastructural changes in disease Hepatocyte (liver cell, parenchymal cell) The nucleus Structural changes Mitochondria Structural changes Endoplasmic reticulum Structural Changes Lysosomes Structural changes Peroxisomes Structural changes Golgi apparatus Structural changes Cell sap (cytosol) Structural changes Bile canaliculus Structural changes Glycogen Structural changes Kupffer cell Structural changes Endothelial cell Structural changes Hepatic stellate cell (Ito cell) Pit cell (large granular lymphocyte) Extracellular vesicles Immunoelectron microscopy Scanning electron microscopy Immunohistochemistry Gene array, gene sequencing and molecular analysis Other Techniques References General reading Glossary Index A B C D E F G H I J K L M N O P Q R S T U V W X Y Z Information about COVID-19 and the liver References Back