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101 Medical Autopsy Cases: Adult & Pediatric

Autor Nandita Bharadwaj Kakkar
en Limba Engleză Hardback – 27 feb 2019
Provides a comprehensive description of 101 medical autopsy cases (48 adult and 53 paediatric) with their complete clinical and pathological details. Each case is unique and has been discussed in a simple, practical, straightforward, but comprehensive manner.
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Specificații

ISBN-13: 9789352706129
ISBN-10: 9352706129
Pagini: 798
Dimensiuni: 216 x 279 mm
Greutate: 2.54 kg
Editura: JAYPEE BROTHERS MEDICAL PUBLISHERS PVT LTD
Colecția Jaypee Brothers,Medical Publishers Pvt. Ltd.
Locul publicării:Delhi, India

Cuprins

Introduction
Medical Autopsy: The Strongest Teaching Tool in Medicine
Section 1: Hematological Disorders—Adult Cases
Case 1: Mantle Cell Lymphoma, Presenting with Florid Cutaneous Lesions, with Common Variant Morphology in the Nodal/Extranodal Sites and Blastoid Morphology in the Peripheral Blood:PM 25983
Case 2: Primary Myelofibrosis, Cellular Phase with Formation of Sclerosing Extramedullary Hematopoietic Tumors: PM 27873
Case 3: Primary Myelofibrosis, Cellular Phase with Extensive Extramedullary Hematopoiesis and Transformation into Acute Leukemia: PM 23618
Case 4: Hepatosplenic T-cell Lymphoma: PM 23096
Case 5: Acute Promyelocytic Leukemia with Early Death due to Disseminated Intravascular Coagulation and Right Temporal Lobe Hemorrhage: PM 26880
Case 6: Acute Promyelocytic Leukemia with Differentiation Syndrome: PM 17959
Case 7: Chronic Lymphatic Leukemia, Post-Bone Marrow Transplantation with Recurrence, Massive Lymphadenopathy and Hemophagocytosis: PM 21710
Case 8: Symptomatic Plasma Cell Myeloma with Primary Systemic Amyloidosis Showing a Predominant Involvement of the Heart and Gastrointestinal Tract: PM 19667
Section 2: Malignancy—Adult Cases
Case 9: Microscopic/Occult Testicular Seminoma with Germ Cell Neoplasia in situ and Widespread Nonseminomatous Metastasis in a Young Male: PM 14170
Case 10:Malignant Teratoma, Primary Pulmonary, Containing Yolk Sac tumor, Associated with Hematologic Neoplasia: PM 13633
Case 11:Young Male with Metastasis: Do not Waste Time—Look for the Primary in the Testes: PM 19388
Case 12: Occult, Peripheral, Mucin-secreting Adenocarcinoma of Lung with Florid Meningeal Carcinomatosis along with Thrombotic Microangiopathy and Disseminated Intravascular Coagulation, Leading to Bilateral Renal Infarction: PM 26226
Case 13: Young Male with Occult, Diffuse Type, Mucin-secreting Adenocarcinoma of the Stomach with Extensive Lymphangitic Carcinomatosis, Presenting with Deep Vein Thrombosis and Pulmonary Embolism: PM 21829
Section 3: Infections—Adult Cases
Case 14: Amebic Ileocolitis, Perforation and Liver Abscess: PM 18836
Case 15: Cerebral Toxoplasmosis in a Human Immunodeficiency Virus Positive Patient: PM 19210
Case 16: Pulmonary Hyalinizing Granuloma with Recent Onset Cryptococcal Meningoencephalitis in an Immunocompetent Male: PM 21122
Case 17: Leptospirosis with Multiorgan Involvement: PM 22793
Case 18: Silicotuberculosis: PM 26075
Case 19: Rabies Meningoencephalitis, Post-Pet Dog Bite: PM 27786
Section 4: Hepatobiliary and Pancreatic Disorders—Adult Cases
Case 20: Extrahepatic Portal Venous Obstruction due to Cavernomatous Transformation of Portal Vein and Portal Cavernoma Cholangiopathy: PM 22260
Case 21: Chronic Budd-Chiari Syndrome with Mesoatrial Shunt, Venocentric Cirrhosis, Hepatocellular Carcinoma Infiltrating into the Hepatic Duct Causing Obstruction and Hemobilia: PM 27800
Case 22: Acute on Chronic Pancreatitis Leading to Portal Vein Pyemia, with Multiple Liver Abscesses and Life-threatening Sepsis Shock: PM 25975
Case 23: Lipomatous Pseudohypertrophy of the Pancreas with Polyglandular Autoimmune Syndrome Type II and Inflammatory Myopathy: PM 22590
Case 24: Young Male with Early Onset Micronodular Cirrhosis due to Synergistic Hepatotoxic Effect of Alcohol and Hepatitis C Virus Infection along with Cryoglobulinemic Vasculitis: PM 27791
Case 25: Diffuse Hepatocellular Carcinoma Arising in a Setting of Mixed Nodular Cirrhosis, Hepatitis C Virus and Alcohol Related: PM 26695
Case 26:Acute Liver Failure and Encephalopathy in a Case of Dengue Shock Syndrome: PM 25035
Case 27: Postpartum, Hyperacute, Fulminant Hepatic Failure due to Hepatitis E Virus: PM 26595
Case 28: Sporadic, Hepatitis E-related Massive Hepatic Necrosis in a Young Female: PM 26254
Case 29: A Classical Case of Wilson’s Disease with Hepatic and Neuropsychiatric Manifestations: PM 26195
Section 5: Cardiovascular System—Adult Cases
Case 30: Silent Healed Myocardial Infarction and its Complications—Infarct Expansion, Mural Thrombosis, Aneurysm Formation, Extensive Arterial Embolization, Deep Vein Thrombosis and Subsequent Fatal Venous Thromboembolism: PM 21817
Case 31: Coexistence of Acute-on-Chronic Rheumatic Heart Disease and Acute Poststreptococcal Glomerulonephritis: PM 21119
Case 32: A Classical Case of Marfan Syndrome with Aortic Root Dilatation, Aneurysm of the Ascending Aorta and Acute Aortic Dissection: PM 22554
Case 33: Adult Tetralogy of Fallot with Tricuspid Valve Infective Endocarditis and Thromboembolic Botryomycotic Cerebral Abscess: PM 26941
Case 34: Cocaine-induced Vasculopathy Leading to Cardiomyopathy, Renal Infarcts, Gangrene of Digits with Autoamputation: PM 23445
Case 35: Aftermath of Hypertension in a Middle-aged Male—Intraparenchymal Brain Hemorrhage, Pontine and Thalamic: PM 26485
Section 6: Systemic Vasculitides—Adult and Pediatric Cases
Systemic Vasculitides—Introduction
Small Vessel Vasculitides
Case 36: Renal Limited Microscopic Polyangiitis: PM 13127
Case 37: Microscopic Polyangiitis, ANCA Negative, with Florid Glomerulitis and Granulomatous Glomerulonephritis: PM 15649
Case 38: Microscopic Polyangiitis in a Child: PM 16450
Case 39: Microscopic Polyangiitis, ANCA Negative, Clinically Mimicking Granulomatosis with Polyangiitis (Wegener’s Granulomatosis) and Presenting with a Breast Mass: PM 18473
Case 40: Microscopic Polyangiitis—Chronic Phase: PM 18987
Case 41: Microscopic Polyangiitis with Acute Vasculitis of Small, Medium and Large-sized Arteries: PM 20415
Case 42: p-ANCA Positive Classic Polyarteritis Nodosa: PM 24277
Case 43: Takayasu’s Aortoarteritis, Pulmonary Hypertension, and Pulmonary Capillary Hemangiomatosis: PM 14993
Case 44: Takayasu Aortoarteritis, Presenting with Pulmonary Arterial Hypertension Secondary to Extensive Involvement of Right Pulmonary Artery: PM 25988
Case 45: Granulomatosis with Polyangiitis (Wegener’s Granulomatosis) with Left Foot Gangrene and Right Hemiplegia: PM 14106
Case 46: Granulomatosis with Polyangiitis—Wegener’s Granulomatosis, Presenting as an Anterior Mediastinal Mass: PM 18613
Case 47: Granulomatosis with Polyangiitis, i.e Wegener’s with Multiple Pulmonary Nodules and Total Splenic Necrosis: PM 21594
Case 48: c-ANCA Positive, Nonreactive, Disseminated Tuberculosis with Pulmonary and Mesenteric Vasculitis: PM 14513
Section 7: Primary Renal Mucormycosis—Adult and Pediatric Cases
Case 49: Isolated Bilateral Renal Mucormycosis with Contiguous Spread to the Adrenals, Mesentery, Pancreas and Colon in an Apparently Immunocompetent Adult: PM 27250
Case 50: Primary Bilateral Renal Mucormycosis in an Apparently Immunocompetent Child: PM 22863
Section 8: Histiocytosis—Pediatric and Adult Cases
Case 51: Primary/Familial Hemophagocytic Lymphohistiocytosis with Extensive Involvement of the Brain: PM 20788
Case 52: Langerhans Cell Histiocytosis Presenting as an Anterior Mediastinal Mass: PM 21476
Case 53: Macrophage Activation Syndrome—A Fatal Complication of Systemic Onset Juvenile Idiopathic Arthritis: PM 26202
Case 54: Epstein–Barr Virus-associated Secondary Hemophagocytic Lymphohistiocytosis—
A Rare Complication: PM 21703
Section 9: Primary Immunodeficiency—Pediatric Cases
Case 55: Disseminated Bacillus Calmette–Guérin Infection in a Case of Severe Combined
Immunodeficiency: PM 22931
Case 56: Chronic Granulomatous Disease of Childhood: PM 24170
Case 57: Disseminated Nonreactive Tuberculosis, PCR-Proven Dual Positivity for Mycobacterium Tuberculosis and Abscessus ? Mendelian Susceptibility to Mycobacterial Disease: PM 25174
Section 10: Infantile Nephrotic Syndrome
Case 58: Congenital Nephrotic Syndrome of the Finnish Type: PM 23777
Case 59: Infantile Nephrotic Syndrome—Diffuse Mesangial Sclerosis in a 10-Month-Old Male Child: PM 26462
Section 11: Infections—Pediatric Cases
Case 60: Disseminated Congenital Cytomegalovirus Infection with Islet Cell Hyperplasia as the Cause of Persistent Hypoglycemia in a Neonate: PM 23822
Case 61: Congenital Tuberculosis: An Underdiagnosed Entity: PM 24753
Case 62: Disseminated Cryptococcomas Mimicking Disseminated Malignancy, with Hepatic Dysfunction as the Initial Manifestation, in an Immunocompetent Child: PM 25744
Introduction to Tubercular Meningitis
Case 63: Catastrophic Posterior Circulation Tubercular Arteritis with Infarcts and Cortical
Venous Thrombosis—A Rare Co-existence: PM 26344
Case 64: Child with Disseminated Miliary Tuberculosis, Tubercular Meningitis with
Extensive Arteritis, Infarction and Ischemic Hepatitis: PM 25901
Case 65: Disseminated Cryptococcal Infection in an HIV-positive Child: PM 23563
Section 12: Cardiovascular System—Pediatric Case
Case 66: Transposition of Great Arteries: PM 24027
Section 13: Hematological Disorders—Pediatric Cases
Case 67: Child with Acute Lymphoblastic Leukemia on Induction Therapy with Febrile
Neutropenia and Disseminated Aspergillus Infection: PM 25927
Case 68: Myeloid Sarcoma of Lacrimal Sac as the First Manifestation of AML-M1 with Acute Diffuse Colorectal Neutropenic Colitis in a Child: PM 23395 576
Section 14: Storage Disorder
Case 69: Niemann–Pick Type B Presenting with Massive Splenohepatomegaly and Hypertensive Crisis in a 12-year-old Child: PM 27096
Section 15: Pediatric Renal Cystic Disease (Developmental/Genetic/Syndromes)
Pediatric Cystic Disease (Developmental/Genetic) of Kidney—Introduction
Section 15A: Renal Dysplasia
Case 70: Recurrent Bilateral Multicystic Dysplastic Kidneys, Consistent with Hereditary
Renal Adysplasia: PM 20505
Case 71: Symmetrically Enlarged, Solid Dysplastic Kidneys with Intrauterine Growth
Retardation: PM 24340
Case 72: Multicystic Dysplastic Kidneys with Dilated Ureters and Hypertrophied Urinary
Bladder Leading to Obstructed Labor and Uterine Rupture: PM 26207
Case 73-74: Renal Hypodysplasia: PM 19521, PM 25711 619
Nandita Bharadwaj Kakkar
Case 75: Bilateral Renal Agenesis: PM 24019
Case 76-80: Unilateral Renal Malformation: PM 22428, PM 22393, PM 26428, PM 26291, PM 26824
Case 81: Segmental Renal Dysplasia with Duplex Kidney and Ureterocele: PM 19965
Section 15B: Posterior Urethral Valve
Case 82-83: Posterior Urethral Valve Leading to Congenital Hydroureteronephrosis and
Hypertrophied Urinary Bladder: PM 18485, PM 26118
Section 15C: Renal Hypoplasia
Case 84: Neonate with Bilateral Simple Renal Hypoplasia, Lung Hypoplasia and Hydrocephalous: PM 27245
Case 85: Bilateral Simple Renal Hypoplasia, Cystic Periventricular Leukomalacia with Hydrocephalus ex vacuo in Surviving Twin, after death of Monochorionic Co-twin: PM 25677
Case 86: Segmental Hypoplasia (Ask-Upmark Kidney): S-14525/2008
Section 15D: Genetic Disorders
Case 87: A Classical Case of Autosomal Recessive Polycystic Kidney Disease: PM 22879
Case 88: Autosomal Dominant Polycystic Kidney Disease with Cyst Infection: PM 22828
Section 15E: Glomerulocystic Kidney Disease
Case 89: Co-existing Glomerulocystic Kidney Disease and Renal Tubular Dysgenesis with Late Onset Oligohydramnios and Renal Failure at D2 of Life: PM 28154
Case 90: Glomerulocystic Kidney Associated with Posterior Urethral Valve— A Rare Association: PM 28255
Section 15F: Syndromes
Case 91-92: Meckel–Gruber Syndrome: PM 20070, PM 26190
Case 93-94: Prune Belly Syndrome Leading to a Markedly Distended Urinary Bladder and
Hydroureteronephrosis: PM 23424, PM 25509
Case 95: Sirenomelia with Bilateral Renal Agenesis and Multiple Other Malformations: PM 27025
Section 16: Liver Disorders—Pediatric Cases
Case 96: Coexistence of Duarte 2 Variant of Galactosemia with Niemann–Pick Disease Type B, in an Infant: PM 23108
Case 97: A Classical Case of Galactosemia: PM 23869
Case 98: Galactosemia, Double Heterozygous for N314D and Q188R Mutations, with
Micronodular Cirrhosis and Absence of Steatosis: PM 25342
Case 99: A Case of Galactosemia, Double Heterozygous for Q188R and E308K Mutations with Early Neonatal Acute Liver Failure: PM 25552
Case 100: Neonate with Hemolytic Disease of Newborn (Due to Rh Isoimmunization—for both Rh-D Antigen and Rh-C Antigen), Conjugated Hyperbilirubinemia, and Associated Nonsyndromic Paucity of Intrahepatic Bile Ducts: PM 27937
Case 101: Indian Childhood Cirrhosis: PM 24527
Abbreviations
Index