LymphedemaV1, PascalFrancis, Corpus, bibRecord, 000A74

Lymphedema : classification, diagnosis and therapy

Identifieur interne : 000A74 ( PascalFrancis/Corpus ); précédent : 000A73; suivant : 000A75

Lymphedema : classification, diagnosis and therapy

Auteurs : A. Szuba ; S. G. Rockson

Source :

Vascular medicine : (London) [ 1358-863X ] ; 1998.

RBID : Pascal:98-0479728

Descripteurs français

Pascal (Inist)
- Lymphoedème, Classification, Symptomatologie, Diagnostic, Traitement, Technique, Homme.

English descriptors

KwdEn :
- Classification, Diagnosis, Human, Lymphedema, Symptomatology, Technique, Treatment.

Abstract

This review presents the diagnostic features, the pathophysiology and the available therapies for lymphedema. This disease is often able to be diagnosed by its characteristic cliniccal presentation, yet, in some cases, ancillary tests might be necessary to establish the diagnosis, particularly in the early stages of the disease and in edemas of mixed etiology. These diagnostic modalities are also useful in clinical studies. Available modalities include isotopic lymphoscintigraphy, indirect and direct lymphography, magnetic resonance imaging, computed tomography and ultrasonography. Lymphedema may be primary or secondary to the presence of other diseases and/or to the consequences of surgery. Primary lymphedema may occur at any phase of life but it most commonly appears at puberty. Secondary lymphedema is encountered more often. The most prevalent worldwide cause of lymphedema is filariasis, which is particularly common in south-east Asia. In the USA, postsurgical lymphedema of the extremity prevails. Complications of chronic limb lymphedema include recurrent cellulitis and lymphangiosarcoma. Most patients are treated conservatively, by means of various forms of compression therapy, including complex physical therapy, pneumatic pumps and compressive garments. Volume reducing surgery is performed rarely. Lymphatic microsurgery is still in an experimental stage, although a few centers consistently report favorable outcomes.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

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A03		`1`		`@0 Vasc. med. : (Lond.)`
A05				`@2 3`
A06				`@2 2`
A08	`01`	`1`	`ENG`	`@1 Lymphedema : classification, diagnosis and therapy`
A11	`01`	`1`		`@1 SZUBA (A.)`
A11	`02`	`1`		`@1 ROCKSON (S. G.)`
A14	`01`			`@1 Division of Cardiovascular Medicine, Stanford University School of Medicine @2 Stanford, CA @3 USA @Z 1 aut. @Z 2 aut.`
A20				`@1 145-156`
A21				`@1 1998`
A23	`01`			`@0 ENG`
A43	`01`			`@1 INIST @2 26454 @5 354000071196710090`
A44				`@0 0000 @1 © 1998 INIST-CNRS. All rights reserved.`
A45				`@0 158 ref.`
A47	`01`	`1`		`@0 98-0479728`
A60				`@1 P`
A61				`@0 A`
A64		`1`		`@0 Vascular medicine : (London)`
A66	`01`			`@0 GBR`
C01	`01`		`ENG`	@0 This review presents the diagnostic features, the pathophysiology and the available therapies for lymphedema. This disease is often able to be diagnosed by its characteristic cliniccal presentation, yet, in some cases, ancillary tests might be necessary to establish the diagnosis, particularly in the early stages of the disease and in edemas of mixed etiology. These diagnostic modalities are also useful in clinical studies. Available modalities include isotopic lymphoscintigraphy, indirect and direct lymphography, magnetic resonance imaging, computed tomography and ultrasonography. Lymphedema may be primary or secondary to the presence of other diseases and/or to the consequences of surgery. Primary lymphedema may occur at any phase of life but it most commonly appears at puberty. Secondary lymphedema is encountered more often. The most prevalent worldwide cause of lymphedema is filariasis, which is particularly common in south-east Asia. In the USA, postsurgical lymphedema of the extremity prevails. Complications of chronic limb lymphedema include recurrent cellulitis and lymphangiosarcoma. Most patients are treated conservatively, by means of various forms of compression therapy, including complex physical therapy, pneumatic pumps and compressive garments. Volume reducing surgery is performed rarely. Lymphatic microsurgery is still in an experimental stage, although a few centers consistently report favorable outcomes.
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C03	`02`	`X`	`FRE`	`@0 Classification @5 04`
C03	`02`	`X`	`ENG`	`@0 Classification @5 04`
C03	`02`	`X`	`GER`	`@0 Klassifizierung @5 04`
C03	`02`	`X`	`SPA`	`@0 Clasificación @5 04`
C03	`03`	`X`	`FRE`	`@0 Symptomatologie @5 07`
C03	`03`	`X`	`ENG`	`@0 Symptomatology @5 07`
C03	`03`	`X`	`SPA`	`@0 Sintomatología @5 07`
C03	`04`	`X`	`FRE`	`@0 Diagnostic @5 08`
C03	`04`	`X`	`ENG`	`@0 Diagnosis @5 08`
C03	`04`	`X`	`SPA`	`@0 Diagnóstico @5 08`
C03	`05`	`X`	`FRE`	`@0 Traitement @5 10`
C03	`05`	`X`	`ENG`	`@0 Treatment @5 10`
C03	`05`	`X`	`GER`	`@0 Aufbereiten @5 10`
C03	`05`	`X`	`SPA`	`@0 Tratamiento @5 10`
C03	`06`	`X`	`FRE`	`@0 Technique @5 11`
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C03	`06`	`X`	`SPA`	`@0 Técnica @5 11`
C03	`07`	`X`	`FRE`	`@0 Homme @5 13`
C03	`07`	`X`	`ENG`	`@0 Human @5 13`
C03	`07`	`X`	`SPA`	`@0 Hombre @5 13`
C07	`01`	`X`	`FRE`	`@0 Appareil circulatoire pathologie @5 37`
C07	`01`	`X`	`ENG`	`@0 Cardiovascular disease @5 37`
C07	`01`	`X`	`SPA`	`@0 Aparato circulatorio patología @5 37`
C07	`02`	`X`	`FRE`	`@0 Lymphatique pathologie @5 38`
C07	`02`	`X`	`ENG`	`@0 Lymphatic vessel disease @5 38`
C07	`02`	`X`	`SPA`	`@0 Linfático patología @5 38`
N21				`@1 313`

Format Inist (serveur)

NO :	PASCAL 98-0479728 INIST
ET :	Lymphedema : classification, diagnosis and therapy
AU :	SZUBA (A.); ROCKSON (S. G.)
AF :	Division of Cardiovascular Medicine, Stanford University School of Medicine/Stanford, CA/Etats-Unis (1 aut., 2 aut.)
DT :	Publication en série; Niveau analytique
SO :	Vascular medicine : (London); ISSN 1358-863X; Royaume-Uni; Da. 1998; Vol. 3; No. 2; Pp. 145-156; Bibl. 158 ref.
LA :	Anglais
EA :	This review presents the diagnostic features, the pathophysiology and the available therapies for lymphedema. This disease is often able to be diagnosed by its characteristic cliniccal presentation, yet, in some cases, ancillary tests might be necessary to establish the diagnosis, particularly in the early stages of the disease and in edemas of mixed etiology. These diagnostic modalities are also useful in clinical studies. Available modalities include isotopic lymphoscintigraphy, indirect and direct lymphography, magnetic resonance imaging, computed tomography and ultrasonography. Lymphedema may be primary or secondary to the presence of other diseases and/or to the consequences of surgery. Primary lymphedema may occur at any phase of life but it most commonly appears at puberty. Secondary lymphedema is encountered more often. The most prevalent worldwide cause of lymphedema is filariasis, which is particularly common in south-east Asia. In the USA, postsurgical lymphedema of the extremity prevails. Complications of chronic limb lymphedema include recurrent cellulitis and lymphangiosarcoma. Most patients are treated conservatively, by means of various forms of compression therapy, including complex physical therapy, pneumatic pumps and compressive garments. Volume reducing surgery is performed rarely. Lymphatic microsurgery is still in an experimental stage, although a few centers consistently report favorable outcomes.
CC :	002B12B03
FD :	Lymphoedème; Classification; Symptomatologie; Diagnostic; Traitement; Technique; Homme
FG :	Appareil circulatoire pathologie; Lymphatique pathologie
ED :	Lymphedema; Classification; Symptomatology; Diagnosis; Treatment; Technique; Human
EG :	Cardiovascular disease; Lymphatic vessel disease
GD :	Klassifizierung; Aufbereiten
SD :	Linfedema; Clasificación; Sintomatología; Diagnóstico; Tratamiento; Técnica; Hombre
LO :	INIST-26454.354000071196710090
ID :	98-0479728

Links to Exploration step

Pascal:98-0479728

Le document en format XML

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<front><div type="abstract" xml:lang="en">This review presents the diagnostic features, the pathophysiology and the available therapies for lymphedema. This disease is often able to be diagnosed by its characteristic cliniccal presentation, yet, in some cases, ancillary tests might be necessary to establish the diagnosis, particularly in the early stages of the disease and in edemas of mixed etiology. These diagnostic modalities are also useful in clinical studies. Available modalities include isotopic lymphoscintigraphy, indirect and direct lymphography, magnetic resonance imaging, computed tomography and ultrasonography. Lymphedema may be primary or secondary to the presence of other diseases and/or to the consequences of surgery. Primary lymphedema may occur at any phase of life but it most commonly appears at puberty. Secondary lymphedema is encountered more often. The most prevalent worldwide cause of lymphedema is filariasis, which is particularly common in south-east Asia. In the USA, postsurgical lymphedema of the extremity prevails. Complications of chronic limb lymphedema include recurrent cellulitis and lymphangiosarcoma. Most patients are treated conservatively, by means of various forms of compression therapy, including complex physical therapy, pneumatic pumps and compressive garments. Volume reducing surgery is performed rarely. Lymphatic microsurgery is still in an experimental stage, although a few centers consistently report favorable outcomes.</div>
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Lymphedema : classification, diagnosis and therapy

Lymphedema : classification, diagnosis and therapy

Source :

Descripteurs français

English descriptors

Abstract

Notice en format standard (ISO 2709)

Format Inist (serveur)

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri