Rottler P, Wilke A, Frangen T M, Kuhnen C, Schley B
Orthopädie und orthopädische Rheumatologie, Elisabeth-Klinik Bigge, Heinrich-Sommer-Straße 4, 59939, Olsberg, Deutschland.
Institut für Pathologie, Clemenshospital Münster, 48153, Münster, Deutschland.
Orthopade. 2017 Apr;46(4):366-369. doi: 10.1007/s00132-017-3396-4.
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.
血管内乳头状内皮增生症(IPEH)/马松假血管肉瘤是一种罕见(孤儿)的前足疾病,在欧洲尚未有相关描述。对一名患有模糊的指间间隙占位性病变的年轻患者进行的病理解剖检查显示为血管内乳头状内皮增生症/马松假血管肉瘤。血管内乳头状内皮增生症主要可在上肢以及颈部检测到。迄今为止,血管内乳头状内皮增生症仅在日本和美国有相关描述。对于欧洲而言,我们的病例报告是对IPEH临床病程的首次描述。