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The series of volumes Progress in Surgical Pathology was conceived
in an attempt to honor the 70th birthday of Dr. Raffaele Lattes.
The original vol umes were the result of an initial call for papers
dedicated to progress in the field of surgical pathology with
contributors from all over the world. The pa pers published in
these volumes have represented examples of classical clin ical
pathologic correlations within the discipline of surgical
pathology; other papers reflect the work being done at the
interface between classical diagnos tic surgical pathology and
research in the realm of immunology, molecular biology, cell
biology, etc. These papers illustrate what is possible utilizing
all of the advances made in basic biology, while remembering that
the patholo gist remains an essential, crucial figure in the
analysis of tissues, both with respect to their diagnosis as weil
as the analysis of the dynamic interactions between cells. There
have also been papers that may be characterized as philosophical or
historical, which Iook at aspects of surgical pathology in a unique
way. Five volumes have been published since 1980. The last of these
was pub lished in 1983. For those of you who have been our loyal
readers, you may wonder why there has been a gap in the publication
of these volumes. This has been due to reorganization both among
ourselves as weil as with the pub lisher."
****VERKAUFSKATEGORIE*** 0 e
Contents: The Use of Immunohistochemistry: Present and Future - The
Expression of Vimentin in Epithelial Neoplasms - Morphologic
Manifestations of Malignant Lymphomas in the Spleen. A Histologic
and Immunohistochemical Study of 500 Biopsy Cases - Demonstration
of Epstein-Barr Viral Genomes in Routine Paraffin Sections of
Lymphoproliferative and Epithelial Lesions by in Situ Hybridization
- Carcinoma of the Lung;Changing Sex Distribution and
Histopathologic Cell Types - Pulmonary Pathology in Lung Transplant
Patients - Bronchiolitis Obliterans with Organizing Pneumonia and
Constrictive Bronchiolitis: Comparative Analysis ofTwo Distinct
Entities - Lymphoid Interstitial Pneunomia in HIV Infected
Individuals. Long-Term Clinicopathologic Observations in 52
Patients and Pathogenesis - Genital Human Papillomavirus (HPV)
Infections and Their Associations with Squamous Cell Cancer:
Reappraisal of the Morphologic, Epidemiologic and DNA Data -
Central and Peripheral Bronchial Carcinoids Possess Distinct
Peptide Immunostaining Patterns - Diagnosis of Rhabdomyosarcomas
with Particular Reference to Immunohistochemical Markers -
Borderline Lesionsof the Gastric Epithelium: New Indicators of
Cancer Risk and Clinical Implications - The Pathology of Secondary
Human Yolk Sac in Spontaneous Abortion: Findings in 103 Cases
This edition is devoted to benign gastrointestinal diseases and
provides an in-depth discussion of many lesions, both common and
uncommon. It is, for the most part, organised by category of
disease rather than by anatomic site. This approach allows for
comprehensive coverage of each entity and avoids redundant
descriptions of lesions that occur in multiple regions of the
gastrointestinal tract. Each disease entity is discussed from the
point of view of its demographics, pathophysiology, clinical
features, gross and microscopic pathology, and treatment. The text
is heavily illustrated with diagrams and gross and microscopic
photographs. Because of the extreme importance of clinical and
endoscopic correlation with interpretation of gastrointestinal
pathologic specimens, a practising gastroenterologist has been
included among the authors. He has added endoscopic pictures and
provides clinical insights critical to the understanding of
gastrointestinal diseases. In many areas, the authors refer to
animal models of disease since these have become powerful tools for
understanding gastrointestinal diseases. They also discuss some of
the molecular alterations that are present as these provide an
understanding of the pathophysiology of the disease. Finally, the
authors discuss the genetic predispositions to gastrointestinal
diseases that occur as a result of genetic loss, mutation,
overexpression of genes, or genetic polymorphisms.
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