L. Penchansky

Pediatric Bone Marrow

• Gebundenes Buch

Produktbeschreibung

No other book covers as extensively the pathology of the bone marrow in children. It provides a wide background for the understanding of bone marrow disease in children and its difference from that of the adult population. It illustrates the morphology of the peripheral blood, bone marrow aspirate and bone marrow biopsy. It is useful for the diagnosis of pediatric disorders in the bone marrow as a guide for pediatric pathologists, hematologists, oncologists and medical technologists or any physician involved in the diagnosis of pediatric bone marrow disorders.

Produktdetails

• Verlag: Springer, Berlin
• 2004
• Seitenzahl: 312
• Erscheinungstermin: 3. Dezember 2003
• Englisch
• Abmessung: 285mm x 215mm x 23mm
• Gewicht: 1138g
• ISBN-13: 9783540442059
• ISBN-10: 3540442057
• Artikelnr.: 12353563

Autorenporträt

Lila Penchansky, Pittsburgh, USA

Inhaltsangabe

1 Normal Bone Marrow.
References.
2 Inherited Bone Marrow Failure.
Inherited Hematopoietic Syndromes Associated with Pancytopenia.
Fanconi Anemia.
Laboratory Findings.
Dyskeratosis Congenita.
Laboratory Findings.
Shwachman
Diamond Syndrome.
Laboratory Findings.
Congenital Amegakaryocytic Thrombocytopenia.
Laboratory Findings.
Rare Familial Marrow Failure Syndromes.
Inherited Hematopoietic Syndromes Associated with Single Cytopenia.
Diamond
Blackfan Anemia.
Laboratory Findings.
Congenital Dyserythropoietic Anemias.
Severe Congenital Neutropenia.
Laboratory Findings.
Cyclic Neutropenia.
Laboratory Findings.
Chronic Benign Neutropenia.
Thrombocytopenia with Absent Radii.
Laboratory Findings.
Inherited Disorders of the Leukocytes Associated with Change in their Morphology.
Pelger
Hüet Anomaly.
May
Hegglin Anomaly.
Chédiak
Higashi Syndrome.
Alder
Reilly Anomaly.
Other Morphological Abnormalities.
Inherited Immunodeficiency.
Reticular Dysgenesis (Alymphocytic Neutropenia).
Laboratory Findings.
X
Linked Agammaglobulinemia (Bruton Agammaglobulinemia).
Laboratory Findings.
Cartilage
Hair Hypoplasia.
Laboratory Findings.
Wiskott
Aldrich Syndrome.
Laboratory Findings.
Omenn Syndrome.
Laboratory Findings.
Inherited Sideroblastic Anemias.
Laboratory Findings.
?
Aminolevulinate Synthase (ALAS2) Deficiency.
Pearson Syndrome.
Osteopetrosis.
Laboratory Findings.
References.
3 Macrophage
and Dendritic
Cell
Related Disorders Including the Lysosomal Storage Disorders.
Storage Disorders.
Gaucher Disease.
Laboratory Findings.
Niemann
Pick Disease.
Laboratory Findings.
Wolman Disease.
Fabry Disease.
Sialidoses.
Gangliosidosis GM1 and GM2.
Fucosidosis.
OC
Mannosidosis.
Glycogen Storage Diseases.
Mucopolysaccharidosis.
Cystinosis.
Primary Hyperoxaluria.
Sea
blue Histiocytosis.
Histiocytosis.
Langerhans Cell Histiocytosis.
Laboratory Findings.
Xanthoma Disseminatum.
Macrophage
Related Disorders.
Hemophagocytic Syndrome.
Laboratory Findings.
References.
4 Bone Marrow Infections.
Infection
Associated Hemophagocytic Syndrome.
Granulomas.
Bacterial Infections.
Mycobacteria.
Ehrlichiosis.
Fungus.
Viruses.
Human Parvovirus B19.
Epstein
Barr
Virus.
Cytomegalovirus.
Human Immune Deficiency Virus.
Human Herpesvirus Type 6.
Other Viruses.
Parasites.
Malaria.
Other Parasites.
References.
5 Bone Marrow Metastases.
Laboratory Findings.
Neuroblastoma.
Laboratory Findings.
Rhabdomyosarcoma.
Laboratory Findings.
wing Family of Tumors.
Laboratory Findings.
Desmoplastic Small Round
Cell Tumor.
Central Nervous System.
Laboratory Findings.
Other Metastatic Tumors.
References.
6 Hematologie Manifestations of Trisomy 21.
Laboratory Findings.
Acute Megakaryoblastic Leukemia (FAB M7).
Laboratory Findings.
Cytochemistry and Immunocytochemistry.
Electron Microscopy.
Cytogenetic and Molecular Genetics.
References.
7 Myelodysplastic Syndromes.
Myelodysplastic and Myeloproliferative Disorders.
Myelodysplastic Syndromes.
Juvenile Myelomonocytic Leukemia.
Laboratory Findings.
Monosomy 7 Syndrome.
Unclassifiable Myelodysplastic Syndromes.
MDSs that Fit the FAB Classification in Children.
Laboratory Findings.
Myeloproliferative Disorders.
Chronic Myelogenous Leukemia.
Laboratory Findings.
Chronic Neutrophilic Leukemia.
Polycythemia Disorders.
Polycythemia Vera.
Laboratory Findings.
Essential Thrombocythemia.
Laboratory Findings.
Hypereosinophilic Syndrome/ Chronic Eosinophilic Leukemia.
Laboratory Findings.
Systemic Mastocytosis.
Laboratory Findings.
References.
8 Acute Myeloid Leukemia.
Acute Myelogenous Leukemia.
Laboratory Findings.
Acute Myeloid Leukemia.
with Minimal Differentiation (FAB Mo).
Acute Myeloid Leukemia without Maturation (FAB M1).
Acute Myeloid Leukemia with Maturation (FABM2).
Acute Promyelocytic Leukemia (FAB M3).
Acute Myelomonocytic Leukemia (FAB M4).
Acute Monoblastic Leukemia (M5).
Acute Erythroleukemia (M6).
Acute Megakaryoblastic Leukemia (M7).
Acute Basophilic Leukemia.
Minimal Residual Disease.
Therapy
Related Acute Leukemia.
Congenital Leukemia.
Recurrent Chromosomal Abnormalities.
Acute Leukemia of Ambiguous Lineage.
References.
9 Acute Lymphoblastic Leukemia and Lymphoma.
Acute Lymphocytic Leukemia/ Lymphoblastic Lymphoma.
Laboratory Findings.
Minimal Residual Disease.
Lymphomas.
Non
Hodgkin Lymphomas.
Large
Cell Lymphomas.
Anaplastic Large
Cell Lymphoma.
Laboratory Findings.
Hodgkin Lymphoma.
Laboratory Findings.
References.
10 Anemias.
Microcytic Anemias.
Iron Deficiency Anemia.
Laboratory Findings.
Macrocytic Anemias.
B12 and Folk Deficiency.
Laboratory Findings.
Normocytic Anemias.
Hemolytic Anemias.
Hereditary Hemolytic Anemias.
Red Blood Cell Membrane Disorders.
Hereditary Spherocytosis.
Laboratory Findings.
Hereditary Elliptocytosis Syndromes.
Laboratory Findings.
Other Inherited Disorders of the Red
Cell Membrane.
Hereditary Anemias Due to Hemoglobin Abnormalities.
Sickle Cell Anemia.
Laboratory Findings.
Thalassemia Syndromes.
?
Thalassemias.
Laboratory Findings.
?
Thalassemias.
Acquired Hemolytic Anemia.
Hemolytic Disease of Newborn.
Laboratory Findings.
Autoimmune Hemolytic Anemia.
Laboratory Findings.
Acquired Non
Immune Hemolytic Anemias.
Paroxysmal Nocturnal Hemoglobinuria.
Transient Erythroblastopenia of Childhood.
Aplastic Anemia.
Laboratory Findings.
References.

Rezensionen

From the reviews:

"The author has succeeded in developing a text atlas that provides a guide to the diagnosis of the common and unusual paediatric haematologic conditions, as well as of non-haematologic disorders that affect the bone marrow. The book is well written, concise and easy to understand. ... This book is a most valuable text atlas for paediatric pathologists, paediatric haematologists and all those involved in the diagnosis of pediatric bone marrow disorders. As a paediatric pathologist, this book is useful for my practice ... ." -- Dr M C Cohen, acpNews, Summer, 2005