Author(s)

Ching-Yueh Lin^1*, Yu-Chun Lin², Liang-Cheng Chen¹, Yung-Tsan Wu¹

¹Department of Physical Medicine and Rehabilitation, Tri-Service General Hospital, National Defense Medical Center, Taipei City.
²Department of Pathology, Tri-Service General Hospital, National Defense Medical Center, Taipei City.

Primary retroperitoneal tumors are rare, and benign retroperitoneal tumors are exceptionally rare. Herein, we present a very rare case of benign concomitant retroperitoneal intramuscular hemangioma and intravascular papillary endothelial hyperplasia, with the unusual presentation of lumbosacral plexopathy. After surgical treatment and rehabilitation, the patient recovered uneventfully. This case report should serve to remind physicians of the rare condition of a retroperitoneal tumor leading to a neurological deficit.

Hemangioma, Intravascular Papillary Endothelial Hyperplasia (IPEH), Lumbosacral Plexopathy, Masson’s Hemangioma, Retroperitoneal Tumor

Lin, C. , Lin, Y. , Chen, L. and Wu, Y. (2014) Concomitant Retroperitoneal Intramuscular Hemangioma and Intravascular Papillary Endothelial Hyperplasia: An Unusual Case Report. Case Reports in Clinical Medicine, 3, 262-266. doi: 10.4236/crcm.2014.35060.