Intravascular papillary endothelial hyperplasia (IPEH) : Masson's pseudoangiosarcoma on the forefoot

Intravascular papillary endothelial hyperplasia (IPEH)/Masson's pseudoangiosarcoma is a rare (orphan) disease of the forefoot that has not yet been described in Europe. The pathoanatomic examination of a young patient with a vague interdigital space-consuming lesion revealed a intravascular pap...

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Bibliographic Details
Published inDer Orthopäde Vol. 46; no. 4; pp. 366 - 369
Main Authors Rottler, P, Wilke, A, Frangen, T M, Kuhnen, C, Schley, B
Format Journal Article
LanguageGerman
Published Germany 01.04.2017
Subjects
Angiomatosis - diagnosis
Angiomatosis - surgery
Diagnosis, Differential
Female
Foot Diseases - diagnosis
Foot Diseases - surgery
Humans
Rare Diseases
Vascular Malformations - diagnosis
Vascular Malformations - surgery
Young Adult
Human forefoot
Differential diagnosis
Neoplasm, vascular
Orphan diseases
Toes
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Summary:Intravascular papillary endothelial hyperplasia (IPEH)/Masson's pseudoangiosarcoma is a rare (orphan) disease of the forefoot that has not yet been described in Europe. The pathoanatomic examination of a young patient with a vague interdigital space-consuming lesion revealed a intravascular papillary endothelial hyperplasia/Masson's pseudoangiosarcoma. The intravascular papillary endothelial hyperplasia can be mainly detected in the upper limbs as well as cervically. Heretofore, the intravascular papillary endothelial hyperplasia has only been described in Japan and the USA. For Europe, our case report is the first description of the clinical course of IPEH.
Bibliography:ObjectType-Case Study-2
SourceType-Scholarly Journals-1
ObjectType-Feature-4
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ISSN:1433-0431
DOI:10.1007/s00132-017-3396-4