Literature DB >> 27894942

Masson Hemangioma-An Unusual Cause of Thoracic Compressive Myelopathy.

Bikash Ranjan Behera1, Rabi Narayan Panda2, Sanjib Mishra2, Manmath Kumar Dhir2.   

Abstract

BACKGROUND: Masson hemangioma is a rare pathologic entity characterized by intravascular papillary endothelial hyperplasia. Although benign, this hemangioma grows to form an expansile compressing mass. This lesion is mostly seen in skin and subcutaneous tissue. Occurrence in the central nervous system is rare. Still rarer is a spinal location with only 5 case reports published to date in the literature. CASE DESCRIPTION: A 32-year-old man presented with paraplegia secondary to extradural compression at the T4-5 level. Histopathologic features were consistent with intravascular papillary endothelial hyperplasia, also known as Masson hemangioma. Differential diagnosis, management, and review of literature are discussed in this report.
CONCLUSIONS: This rare pathology should be in the differential diagnosis when spinal cord compressive myelopathy is encountered.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Intravascular papillary endothelial hyperplasia; Masson hemangioma; Spinal cord compression

Mesh:

Year:  2016        PMID: 27894942     DOI: 10.1016/j.wneu.2016.11.099

Source DB:  PubMed          Journal:  World Neurosurg        ISSN: 1878-8750            Impact factor:   2.104


  2 in total

1.  Intravascular papillary endothelial hyperplasia as a rare cause of cervicothoracic spinal cord compression: A case report.

Authors:  Hong-Lin Gu; Xiao-Qing Zheng; Shi-Qiang Zhan; Yun-Bing Chang
Journal:  World J Clin Cases       Date:  2021-12-06       Impact factor: 1.337

2.  Masson's Hemangioma of the Urethra: A Case Report.

Authors:  Khadijeh Abdal; Mohammadreza Hafezi Ahmadi
Journal:  Iran J Med Sci       Date:  2018-05
  2 in total

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