By Laura Lamps
Designed as an easy-to-use and entire reference for the training pathologist, Diagnostic Pathology: Hepatobiliary and Pancreas is the following hugely expected name within the Diagnostic Pathology sequence provided by means of Amirsys. As readers have come to count on from this sequence, Diagnostic Pathology: Hepatobiliary and Pancreas is stuffed with more desirable clinical pictures, together with gross pictures, photomicrographs, and targeted clinical illustrations. As with our different Diagnostic Pathology titles, chapters contain definitions, terminology, etiologies and pathogenesis, demographics, medical shows, remedy, prognoses, radiologic imaging, pathology, and differential diagnoses. The pathologic positive aspects are generally exact with descriptions of the macroscopic positive aspects, microscopic findings, cytopathology (as indicated), and as wanted, ancillary experiences. The latter comprise histochemistry, immunohistochemistry, cytogenetics, molecular diagnostics and ultrastructural findings. There also are a number of quick-reference attempt info tables, in addition to valuable introductory chapters, annotated and illustrated staging templates, and chapters on specimen exam dealing with. This good-looking quantity is a veritable one-stop store on your hepatic, biliary, and pancreatic pathology reference wishes.
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Extra info for Diagnostic Pathology: Hepatobiliary & Pancreas
I(1):27 Image Gallery Microscopic Features of PFIC2 (BSEP Deficiency) (Left) Biopsy in an infant with PFIC2 (BSEP deficiency) shows nodule formation and portal inflammation. (Right) Higher magnification of a biopsy in an infant with PFIC2 (BSEP deficiency) shows perinodular inflammation and bile pigment within hepatocytes . 53 Diagnostic Pathology: Hepatobiliary and Pancreatic (Left) Biopsy in an infant with PFIC2 (BSEP deficiency) shows bile plugs within canaliculi , inflammation, and extramedullary hematopoiesis .
Semin Liver Dis. 21(4):551-62, 2001 6. Thompson R et al: BSEP: function and role in progressive familial intrahepatic cholestasis. Semin Liver Dis. 21(4):545-50, 2001 7. van Mil SW et al: FIC1 disease: a spectrum of intrahepatic cholestatic disorders. Semin Liver Dis. 21(4):535-44, 2001 8. Alonso EM et al: Histologic pathology of the liver in progressive familial intrahepatic cholestasis. J Pediatr Gastroenterol Nutr. I(1):27 Image Gallery Microscopic Features of PFIC2 (BSEP Deficiency) (Left) Biopsy in an infant with PFIC2 (BSEP deficiency) shows nodule formation and portal inflammation.
55(2):81-3, 2001 5. Ishihara T et al: Role of UGT1A1 mutation in fasting hyperbilirubinemia. J Gastroenterol Hepatol. 16(6):678-82, 2001 6. Kadakol A et al: Genetic lesions of bilirubin uridinediphosphoglucuronate glucuronosyltransferase (UGT1A1) causing Crigler-Najjar and Gilbert syndromes: correlation of genotype to phenotype. Hum Mutat. 16(4):297-306, 2000 Image Gallery 46 Diagnostic Pathology: Hepatobiliary and Pancreatic (Left) Fontana-Masson stain highlights the increased lipofuscin marked by black staining in the centrilobular hepatocytes.