LymphedemaV1, PascalFrancis, Corpus, bibRecord, 000D54

Angiosarcoma in congenital hereditary lymphoedema (Milroy's disease) : diagnostic beacons and a review of the literature

Identifieur interne : 000D54 ( PascalFrancis/Corpus ); précédent : 000D53; suivant : 000D55

Angiosarcoma in congenital hereditary lymphoedema (Milroy's disease) : diagnostic beacons and a review of the literature

Auteurs : T. W. Offori ; C. C. Platt ; M. Stephens ; G. B. Hopkinson

Source :

Clinical and experimental dermatology [ 0307-6938 ] ; 1993.

RBID : Pascal:93-0352233

Descripteurs français

Pascal (Inist)
- Lymphoedème, Angiosarcome, Congénital, Complication, Diagnostic, Immunohistochimie, Histochimie, Anatomopathologie, Exploration, Etude cas.

English descriptors

KwdEn :
- Angiosarcoma, Case study, Complication, Congenital, Diagnosis, Exploration, Histochemistry, Immunohistochemistry, Lymphedema, Pathology.

Abstract

In cases of congenital lymphoedema the finding of ulceration, violaceous nodules or papules, or apparent traumatic ecchymoses¹ should act as a diagnostic beacon warning of dangers. A case is reported of a high-grade angiosarcoma developing in a patient with congenital hereditary lymphoedema (Milroy's disease). This is the second paper to report this complication, the third case report and the first case in which the diagnosis is substantiated by immunohistochemistry and lectin histochemistry. A review of cases of angiosarcoma complicating congenital hereditary and non-hereditary lymphoedema is also presented

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

A01	`01`	`1`		`@0 0307-6938`
A02	`01`			`@0 CEDEDE`
A03		`1`		`@0 Clin. exp. dermatol.`
A05				`@2 18`
A06				`@2 2`
A08	`01`	`1`	`ENG`	`@1 Angiosarcoma in congenital hereditary lymphoedema (Milroy's disease) : diagnostic beacons and a review of the literature`
A11	`01`	`1`		`@1 OFFORI (T. W.)`
A11	`02`	`1`		`@1 PLATT (C. C.)`
A11	`03`	`1`		`@1 STEPHENS (M.)`
A11	`04`	`1`		`@1 HOPKINSON (G. B.)`
A14	`01`			`@1 North Staffordshire hosp. cent., dep. surgery @2 Stroke-on-Trent @3 GBR @Z 1 aut. @Z 4 aut.`
A20				`@1 174-177`
A21				`@1 1993`
A23	`01`			`@0 ENG`
A43	`01`			`@1 INIST @2 16224 @5 354000037105150240`
A44				`@0 0000`
A45				`@0 20 ref.`
A47	`01`	`1`		`@0 93-0352233`
A60				`@1 P @3 EC`
A61				`@0 A`
A64		`1`		`@0 Clinical and experimental dermatology`
A66	`01`			`@0 GBR`
C01	`01`		`ENG`	@0 In cases of congenital lymphoedema the finding of ulceration, violaceous nodules or papules, or apparent traumatic ecchymoses¹ should act as a diagnostic beacon warning of dangers. A case is reported of a high-grade angiosarcoma developing in a patient with congenital hereditary lymphoedema (Milroy's disease). This is the second paper to report this complication, the third case report and the first case in which the diagnosis is substantiated by immunohistochemistry and lectin histochemistry. A review of cases of angiosarcoma complicating congenital hereditary and non-hereditary lymphoedema is also presented
C02	`01`	`X`		`@0 002B12B04`
C03	`01`	`X`	`FRE`	`@0 Lymphoedème @2 NM @2 L1`
C03	`01`	`X`	`ENG`	`@0 Lymphedema @2 NM @2 L1`
C03	`01`	`X`	`SPA`	`@0 Linfedema @2 NM @2 L1`
C03	`02`	`X`	`FRE`	`@0 Angiosarcome @2 NM`
C03	`02`	`X`	`ENG`	`@0 Angiosarcoma @2 NM`
C03	`02`	`X`	`SPA`	`@0 Angiosarcoma @2 NM`
C03	`03`	`X`	`FRE`	`@0 Congénital @2 L1`
C03	`03`	`X`	`ENG`	`@0 Congenital @2 L1`
C03	`03`	`X`	`SPA`	`@0 Congénito @2 L1`
C03	`04`	`X`	`FRE`	`@0 Complication`
C03	`04`	`X`	`ENG`	`@0 Complication`
C03	`04`	`X`	`SPA`	`@0 Complicación`
C03	`05`	`X`	`FRE`	`@0 Diagnostic`
C03	`05`	`X`	`ENG`	`@0 Diagnosis`
C03	`05`	`X`	`SPA`	`@0 Diagnóstico`
C03	`06`	`X`	`FRE`	`@0 Immunohistochimie`
C03	`06`	`X`	`ENG`	`@0 Immunohistochemistry`
C03	`06`	`X`	`SPA`	`@0 Inmunohistoquímica`
C03	`07`	`X`	`FRE`	`@0 Histochimie`
C03	`07`	`X`	`ENG`	`@0 Histochemistry`
C03	`07`	`X`	`SPA`	`@0 Histoquímica`
C03	`08`	`X`	`FRE`	`@0 Anatomopathologie`
C03	`08`	`X`	`ENG`	`@0 Pathology`
C03	`08`	`X`	`SPA`	`@0 Anatomía patológica`
C03	`09`	`X`	`FRE`	`@0 Exploration`
C03	`09`	`X`	`ENG`	`@0 Exploration`
C03	`09`	`X`	`SPA`	`@0 Exploración`
C03	`10`	`X`	`FRE`	`@0 Etude cas`
C03	`10`	`X`	`ENG`	`@0 Case study`
C03	`10`	`X`	`SPA`	`@0 Estudio caso`
C07	`01`	`X`	`FRE`	`@0 Appareil circulatoire pathologie`
C07	`01`	`X`	`ENG`	`@0 Cardiovascular disease`
C07	`01`	`X`	`SPA`	`@0 Aparato circulatorio patología`
C07	`02`	`X`	`FRE`	`@0 Lymphatique pathologie`
C07	`02`	`X`	`ENG`	`@0 Lymphatic vessel disease`
C07	`02`	`X`	`SPA`	`@0 Linfático patología`
C07	`03`	`X`	`FRE`	`@0 Peau pathologie`
C07	`03`	`X`	`ENG`	`@0 Skin disease`
C07	`03`	`X`	`SPA`	`@0 Piel patología`
C07	`04`	`X`	`FRE`	`@0 Maladie congénitale`
C07	`04`	`X`	`ENG`	`@0 Congenital disease`
C07	`04`	`X`	`SPA`	`@0 Enfermedad congénita`
C07	`05`	`X`	`FRE`	`@0 Vaisseau sanguin pathologie`
C07	`05`	`X`	`ENG`	`@0 Vascular disease`
C07	`05`	`X`	`SPA`	`@0 Vaso sanguíneo patología`
C07	`06`	`X`	`FRE`	`@0 Tumeur maligne`
C07	`06`	`X`	`ENG`	`@0 Malignant tumor`
C07	`06`	`X`	`SPA`	`@0 Tumor maligno`
C07	`07`	`X`	`FRE`	`@0 Homme`
C07	`07`	`X`	`ENG`	`@0 Human`
C07	`07`	`X`	`SPA`	`@0 Hombre`
C07	`08`	`X`	`FRE`	`@0 Femelle`
C07	`08`	`X`	`ENG`	`@0 Female`
C07	`08`	`X`	`SPA`	`@0 Hembra`
N21				`@1 132`

Format Inist (serveur)

NO :	PASCAL 93-0352233 INIST
ET :	Angiosarcoma in congenital hereditary lymphoedema (Milroy's disease) : diagnostic beacons and a review of the literature
AU :	OFFORI (T. W.); PLATT (C. C.); STEPHENS (M.); HOPKINSON (G. B.)
AF :	North Staffordshire hosp. cent., dep. surgery/Stroke-on-Trent/Royaume-Uni (1 aut., 4 aut.)
DT :	Publication en série; Etude de cas, cas et faits cliniques; Niveau analytique
SO :	Clinical and experimental dermatology; ISSN 0307-6938; Coden CEDEDE; Royaume-Uni; Da. 1993; Vol. 18; No. 2; Pp. 174-177; Bibl. 20 ref.
LA :	Anglais
EA :	In cases of congenital lymphoedema the finding of ulceration, violaceous nodules or papules, or apparent traumatic ecchymoses¹ should act as a diagnostic beacon warning of dangers. A case is reported of a high-grade angiosarcoma developing in a patient with congenital hereditary lymphoedema (Milroy's disease). This is the second paper to report this complication, the third case report and the first case in which the diagnosis is substantiated by immunohistochemistry and lectin histochemistry. A review of cases of angiosarcoma complicating congenital hereditary and non-hereditary lymphoedema is also presented
CC :	002B12B04
FD :	Lymphoedème; Angiosarcome; Congénital; Complication; Diagnostic; Immunohistochimie; Histochimie; Anatomopathologie; Exploration; Etude cas
FG :	Appareil circulatoire pathologie; Lymphatique pathologie; Peau pathologie; Maladie congénitale; Vaisseau sanguin pathologie; Tumeur maligne; Homme; Femelle
ED :	Lymphedema; Angiosarcoma; Congenital; Complication; Diagnosis; Immunohistochemistry; Histochemistry; Pathology; Exploration; Case study
EG :	Cardiovascular disease; Lymphatic vessel disease; Skin disease; Congenital disease; Vascular disease; Malignant tumor; Human; Female
SD :	Linfedema; Angiosarcoma; Congénito; Complicación; Diagnóstico; Inmunohistoquímica; Histoquímica; Anatomía patológica; Exploración; Estudio caso
LO :	INIST-16224.354000037105150240
ID :	93-0352233

Links to Exploration step

Pascal:93-0352233

Le document en format XML

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<front><div type="abstract" xml:lang="en">In cases of congenital lymphoedema the finding of ulceration, violaceous nodules or papules, or apparent traumatic ecchymoses<sup>1</sup>
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<server><NO>PASCAL 93-0352233 INIST</NO>
<ET>Angiosarcoma in congenital hereditary lymphoedema (Milroy's disease) : diagnostic beacons and a review of the literature</ET>
<AU>OFFORI (T. W.); PLATT (C. C.); STEPHENS (M.); HOPKINSON (G. B.)</AU>
<AF>North Staffordshire hosp. cent., dep. surgery/Stroke-on-Trent/Royaume-Uni (1 aut., 4 aut.)</AF>
<DT>Publication en série; Etude de cas, cas et faits cliniques; Niveau analytique</DT>
<SO>Clinical and experimental dermatology; ISSN 0307-6938; Coden CEDEDE; Royaume-Uni; Da. 1993; Vol. 18; No. 2; Pp. 174-177; Bibl. 20 ref.</SO>
<LA>Anglais</LA>
<EA>In cases of congenital lymphoedema the finding of ulceration, violaceous nodules or papules, or apparent traumatic ecchymoses<sup>1</sup>
 should act as a diagnostic beacon warning of dangers. A case is reported of a high-grade angiosarcoma developing in a patient with congenital hereditary lymphoedema (Milroy's disease). This is the second paper to report this complication, the third case report and the first case in which the diagnosis is substantiated by immunohistochemistry and lectin histochemistry. A review of cases of angiosarcoma complicating congenital hereditary and non-hereditary lymphoedema is also presented</EA>
<CC>002B12B04</CC>
<FD>Lymphoedème; Angiosarcome; Congénital; Complication; Diagnostic; Immunohistochimie; Histochimie; Anatomopathologie; Exploration; Etude cas</FD>
<FG>Appareil circulatoire pathologie; Lymphatique pathologie; Peau pathologie; Maladie congénitale; Vaisseau sanguin pathologie; Tumeur maligne; Homme; Femelle</FG>
<ED>Lymphedema; Angiosarcoma; Congenital; Complication; Diagnosis; Immunohistochemistry; Histochemistry; Pathology; Exploration; Case study</ED>
<EG>Cardiovascular disease; Lymphatic vessel disease; Skin disease; Congenital disease; Vascular disease; Malignant tumor; Human; Female</EG>
<SD>Linfedema; Angiosarcoma; Congénito; Complicación; Diagnóstico; Inmunohistoquímica; Histoquímica; Anatomía patológica; Exploración; Estudio caso</SD>
<LO>INIST-16224.354000037105150240</LO>
<ID>93-0352233</ID>
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Angiosarcoma in congenital hereditary lymphoedema (Milroy's disease) : diagnostic beacons and a review of the literature

Angiosarcoma in congenital hereditary lymphoedema (Milroy's disease) : diagnostic beacons and a review of the literature

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