Causes and consequences of lymphatic disease.
Identifieur interne : 003E97 ( Ncbi/Curation ); précédent : 003E96; suivant : 003E98Causes and consequences of lymphatic disease.
Auteurs : Stanley G. Rockson [États-Unis]Source :
- Annals of the New York Academy of Sciences [ 1749-6632 ] ; 2010.
Descripteurs français
- KwdFr :
- MESH :
- anatomopathologie : Maladies lymphatiques.
- physiopathologie : Maladies lymphatiques.
- étiologie : Maladies lymphatiques.
- Homéostasie, Humains.
English descriptors
- KwdEn :
- MESH :
- etiology : Lymphatic Diseases.
- pathology : Lymphatic Diseases.
- physiopathology : Lymphatic Diseases.
- Homeostasis, Humans.
Abstract
The visceral manifestations of lymphatic disorders (lymphangiomatosis and lymphangiectasia) are particularly severe. Any pathology of the lymphatic vasculature, whether superficial or internal, regional, or systemic, is predominated by the appearance of lymphedema, the characteristic form of tissue edema that occurs when lymphatic dysfunction supervenes. Disease manifestations may include dysregulation of body fluid homeostasis, immune traffic impairment, and disturbances of lipid and protein reabsorption from the gut lumen. The appearance of lymphatic edema invokes complex biological alterations. Many of these changes seem to relate uniquely to chronic lymphatic edema, including a profound stimulus to collagen and adipose deposition. Despite the recent advances in our understanding of these disorders, substantial knowledge gaps remain; these gaps inhibit our ability to accurately identify, categorize, treat, and prevent these diseases. Future diagnostic, therapeutic, and reproductive decisions for affected individuals require an accurate knowledge of the clinical and laboratory presentation, mode of inheritance, treatment response, outcomes, and prognosis.
DOI: 10.1111/j.1749-6632.2010.05804.x
PubMed: 20961302
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Rockson</name><affiliation wicri:level="1"><nlm:affiliation>Center for Lymphatic and Venous Disorders, Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, California 94305, USA. rockson@stanford.edu</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Center for Lymphatic and Venous Disorders, Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, California 94305</wicri:regionArea><wicri:noRegion>California 94305</wicri:noRegion></affiliation></author></analytic><series><title level="j">Annals of the New York Academy of Sciences</title><idno type="eISSN">1749-6632</idno><imprint><date when="2010" type="published">2010</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Homeostasis</term><term>Humans</term><term>Lymphatic Diseases (etiology)</term><term>Lymphatic Diseases (pathology)</term><term>Lymphatic Diseases (physiopathology)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Homéostasie</term><term>Humains</term><term>Maladies lymphatiques (anatomopathologie)</term><term>Maladies lymphatiques (physiopathologie)</term><term>Maladies lymphatiques (étiologie)</term></keywords><keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Maladies lymphatiques</term></keywords><keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Lymphatic Diseases</term></keywords><keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Lymphatic Diseases</term></keywords><keywords scheme="MESH" qualifier="physiopathologie" xml:lang="fr"><term>Maladies lymphatiques</term></keywords><keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Lymphatic Diseases</term></keywords><keywords scheme="MESH" qualifier="étiologie" xml:lang="fr"><term>Maladies lymphatiques</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Homeostasis</term><term>Humans</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Homéostasie</term><term>Humains</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The visceral manifestations of lymphatic disorders (lymphangiomatosis and lymphangiectasia) are particularly severe. Any pathology of the lymphatic vasculature, whether superficial or internal, regional, or systemic, is predominated by the appearance of lymphedema, the characteristic form of tissue edema that occurs when lymphatic dysfunction supervenes. Disease manifestations may include dysregulation of body fluid homeostasis, immune traffic impairment, and disturbances of lipid and protein reabsorption from the gut lumen. The appearance of lymphatic edema invokes complex biological alterations. Many of these changes seem to relate uniquely to chronic lymphatic edema, including a profound stimulus to collagen and adipose deposition. Despite the recent advances in our understanding of these disorders, substantial knowledge gaps remain; these gaps inhibit our ability to accurately identify, categorize, treat, and prevent these diseases. Future diagnostic, therapeutic, and reproductive decisions for affected individuals require an accurate knowledge of the clinical and laboratory presentation, mode of inheritance, treatment response, outcomes, and prognosis.</div></front></TEI></record>Pour manipuler ce document sous Unix (Dilib)
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