LymphedemaV1, Main, Exploration, bibRecord, 00C622

Endovascular papillary angioendothelioma‐like tumour associated with lymphoedema

Identifieur interne : 00C622 ( Main/Exploration ); précédent : 00C621; suivant : 00C623

Endovascular papillary angioendothelioma‐like tumour associated with lymphoedema

Auteurs : M. Fukunaga [Japon] ; S. Ushigome [Japon] ; Y. Shishikura [Japon] ; K. Yokoi [Japon] ; E. Ishikawa [Japon]

Source :

Histopathology [ 0309-0167 ] ; 1995-09.

RBID : ISTEX:DBF179368886F4C758F2F3A9754F320163955645

Descripteurs français

KwdFr :
- Arthropathie nerveuse (), Articulation du coude, Femelle, Humains, Hémangioendothéliome (), Hémangioendothéliome (anatomopathologie), Lymphoedème (), Lymphoedème (anatomopathologie), Sujet âgé, Tumeurs vasculaires (), Tumeurs vasculaires (anatomopathologie).
MESH :
- anatomopathologie : Hémangioendothéliome, Lymphoedème, Tumeurs vasculaires.
Pascal (Inist)
- Arthropathie nerveuse, Articulation du coude, Association morbide, Etude cas, Femelle, Homme, Humains, Hémangioendothéliome, Hémangioendothéliome végétant intravasculaire, Immunohistochimie, Lymphoedème, Sujet âgé, Tumeurs vasculaires.
Wicri :
- topic : Homme.

English descriptors

KwdEn :
- Aged, Arthropathy, Neurogenic (complications), Case study, Concomitant disease, Elbow Joint, Female, Hemangioendothelioma (complications), Hemangioendothelioma (pathology), Human, Humans, Immunohistochemistry, Lymphedema, Lymphedema (complications), Lymphedema (pathology), Vascular Neoplasms (chemistry), Vascular Neoplasms (complications), Vascular Neoplasms (pathology), Vegetant intravascular hemangioendothelioma.
MESH :
- chemistry : Vascular Neoplasms.
- complications : Arthropathy, Neurogenic, Hemangioendothelioma, Lymphedema, Vascular Neoplasms.
- pathology : Hemangioendothelioma, Lymphedema, Vascular Neoplasms.
- Aged, Elbow Joint, Female, Humans.

Abstract

A case of endovascular papillary angioendothelioma‐like tumour associated with lymphoedema is described. Microscopically, the tumour was composed of anastomosing vascular channels, some of which contained papillary projections, producing tuft‐like or glomeruloid appearances. The dermis also showed moderate lymphoedema and lymphocyic infiltrate. The tumour resembled endovascular papillary angioendothelioma but also had several features that differed from typical examples: occurrence in an old patient and less prominent endothelial hobnail features and lymphocytic infiltrate. Three types of proliferating cells were observed: 1 mature flattened endothelial cells, which were strongly positive for endothelial markers (factor VIII‐related antigen, CD31, CD34) and bound ulex europaeus agglutinin 1; 2 immature endothelial cells with round nuclei and vacuolated or pale cytoplasm, which were strongly positive for CD31 and muscle‐specific actin (HHF35) and focally positive for other endothelial markers; and 3 stromal spindle cells in papillary or glomeruloid areas, which were positive for vimentin, HHF35, and alpha‐smooth muscle actin but negative for desmin. The tumour was diploid by flow cytometry. The patient was well without disease twelve months after the excision. We postulate that this tumour was caused by circulatory disturbance, namely lymphoedema associated with syringomyelia and a Charcot's joint.

Url:

https://api.istex.fr/document/DBF179368886F4C758F2F3A9754F320163955645/fulltext/pdf

DOI: 10.1111/j.1365-2559.1995.tb00216.x

Affiliations:

Le document en format XML

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<front><div type="abstract">A case of endovascular papillary angioendothelioma‐like tumour associated with lymphoedema is described. Microscopically, the tumour was composed of anastomosing vascular channels, some of which contained papillary projections, producing tuft‐like or glomeruloid appearances. The dermis also showed moderate lymphoedema and lymphocyic infiltrate. The tumour resembled endovascular papillary angioendothelioma but also had several features that differed from typical examples: occurrence in an old patient and less prominent endothelial hobnail features and lymphocytic infiltrate. Three types of proliferating cells were observed: 1 mature flattened endothelial cells, which were strongly positive for endothelial markers (factor VIII‐related antigen, CD31, CD34) and bound ulex europaeus agglutinin 1; 2 immature endothelial cells with round nuclei and vacuolated or pale cytoplasm, which were strongly positive for CD31 and muscle‐specific actin (HHF35) and focally positive for other endothelial markers; and 3 stromal spindle cells in papillary or glomeruloid areas, which were positive for vimentin, HHF35, and alpha‐smooth muscle actin but negative for desmin. The tumour was diploid by flow cytometry. The patient was well without disease twelve months after the excision. We postulate that this tumour was caused by circulatory disturbance, namely lymphoedema associated with syringomyelia and a Charcot's joint.</div>
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Serveur d'exploration sur le lymphœdème

Endovascular papillary angioendothelioma‐like tumour associated with lymphoedema

Endovascular papillary angioendothelioma‐like tumour associated with lymphoedema

Source :

Descripteurs français

English descriptors

Abstract

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