Recently characterized vascular tumours of skin and soft tissues
Identifieur interne : 00D731 ( Main/Exploration ); précédent : 00D730; suivant : 00D732Recently characterized vascular tumours of skin and soft tissues
Auteurs : W. Y. W. Tsang [Royaume-Uni] ; J. K. C. Chan [Royaume-Uni] ; C. D. M. Fletcher [Royaume-Uni]Source :
- Histopathology [ 0309-0167 ] ; 1991-12.
Abstract
This review summarizes the clinicopathological features of a number of vascular tumours that have been characterized only in recent years. These include: glomeruloid haemangioma. a multifocal vascular lesion associated with POEMS syndrome; Kaposi‐like infantile haemangioendothelioma, a borderline malignant tumour occurring in the retroperitoneum of infants, mimicking Kaposi's sarcoma histologically; giant cell angioblastoma, characterized by proliferated vessels with a granuloma‐like appearance; benign lymphangioendothelioma (progressive lymphan‐gioma), a slowly‐growing macule or plaque over the trunk or limb, mimicking low‐grade angiosarcoma histologically; largetoid haemosiderotic haemangioma. a benign lesion with a distinctive annular appearance and histologically overlapping with benign lymphangioendothelioma; spindle cell haemangioendothelioma, a lesion located mostly in the distal extremities, characterized by cavernous vascular spaces, spindle cells with interspersed narrow vascular channels and scattered plump vacuolated endothelial cells; acquired tufted angioma. characterized by ‘cannon‐ball’; involve aent of the dermis by lobules of pericyte‐rich capillaries: sinusoidal haemangioma, a distinctive variant of cavernous haemangioma which may be confused with angiosarcoma; and epithelioid angiosarcoma, a highly aggressive tumour of deep soft tissue mimicking metastatic carcinoma and co‐expressing endothelial and epithelial markers.
Url:
DOI: 10.1111/j.1365-2559.1991.tb01497.x
Affiliations:
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Le document en format XML
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<front><div type="abstract" xml:lang="en">This review summarizes the clinicopathological features of a number of vascular tumours that have been characterized only in recent years. These include: glomeruloid haemangioma. a multifocal vascular lesion associated with POEMS syndrome; Kaposi‐like infantile haemangioendothelioma, a borderline malignant tumour occurring in the retroperitoneum of infants, mimicking Kaposi's sarcoma histologically; giant cell angioblastoma, characterized by proliferated vessels with a granuloma‐like appearance; benign lymphangioendothelioma (progressive lymphan‐gioma), a slowly‐growing macule or plaque over the trunk or limb, mimicking low‐grade angiosarcoma histologically; largetoid haemosiderotic haemangioma. a benign lesion with a distinctive annular appearance and histologically overlapping with benign lymphangioendothelioma; spindle cell haemangioendothelioma, a lesion located mostly in the distal extremities, characterized by cavernous vascular spaces, spindle cells with interspersed narrow vascular channels and scattered plump vacuolated endothelial cells; acquired tufted angioma. characterized by ‘cannon‐ball’; involve aent of the dermis by lobules of pericyte‐rich capillaries: sinusoidal haemangioma, a distinctive variant of cavernous haemangioma which may be confused with angiosarcoma; and epithelioid angiosarcoma, a highly aggressive tumour of deep soft tissue mimicking metastatic carcinoma and co‐expressing endothelial and epithelial markers.</div>
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