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A Case of Multiple Intravascular Papillary Endothelial Hyperplasia / 대한피부과학회지
Korean Journal of Dermatology ; : 375-378, 2005.
Article in Korean | WPRIM | ID: wpr-192716
ABSTRACT
Intravascular papillary endothelial hyperplasia (IPEH), also known as Masson's pseudoangiosarcoma, is an unusual pattern of organization of a thrombus within a vein, or within one or more of the component vessels of various vascular abnormalities, such as cavernous hemangioma, pyogenic granuloma and lymphangioma. It is characterized by the development of endothelial-lined papillary projections in a vascular lumen. Lesions of IPEH usually occur on the head, neck or upper extremities as a solitary reddish or bluish nodule. Herein we report a 34-year-old female who presented with multiple bluish nodules on the left hand, which upon histopathological examination showed intravascular papillary endothelial hyperplasia.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Thrombosis / Veins / Granuloma, Pyogenic / Upper Extremity / Hand / Head / Hemangioma, Cavernous / Hyperplasia / Lymphangioma / Neck Limits: Adult / Female / Humans Language: Korean Journal: Korean Journal of Dermatology Year: 2005 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Thrombosis / Veins / Granuloma, Pyogenic / Upper Extremity / Hand / Head / Hemangioma, Cavernous / Hyperplasia / Lymphangioma / Neck Limits: Adult / Female / Humans Language: Korean Journal: Korean Journal of Dermatology Year: 2005 Type: Article