Literature DB >> 11147847

Intraspinal osteolipoma. Case report.

Y C Lin1, C C Huang, H J Chen.   

Abstract

Lipomatous tumors can contain uncommon or rare components (such as fibrolipoma or angiolipoma) that may result in the development of symptoms. To the best of the authors' knowledge, lipoma associated with an osseous component has not been previously reported. A case of intraspinal extradural tumor composed of both adipose and bone tissue is presented. Current theories on the cause of lipoma with an osseous component are discussed. The tumor was histologically confirmed to be an osteolipoma, and the patient recovered well after resection.

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Year:  2001        PMID: 11147847     DOI: 10.3171/spi.2001.94.1.0126

Source DB:  PubMed          Journal:  J Neurosurg        ISSN: 0022-3085            Impact factor:   5.115


  5 in total

Review 1.  Osteochondrolipoma of the submandibular region: a case report and review of the literature.

Authors:  Raoulin Soulard; Anh Tuan Nguyen; Jean-Baptiste Souraud; Pierre-Antoine Oddon; Bernard Fouet; Olivier Cathelinaud
Journal:  Head Neck Pathol       Date:  2012-05-24

2.  Cervical paravertebral osteolipoma: case report and literature review.

Authors:  Pau Guirro; Guillem Saló; Antoni Molina; Andreu Lladó; Lluís Puig-Verdié; Manuel Ramírez-Valencia
Journal:  Asian Spine J       Date:  2015-04-15

3.  Isolated dorsal column dysfunction due to an intraspinal Osteolipoma - Case report and review of literature.

Authors:  Siddharth N Aiyer; Ajoy Prasad Shetty; Rishi Kanna; Anupama Maheswaran; S Rajasekaran
Journal:  J Clin Orthop Trauma       Date:  2016-11-29

4.  Pure intramuscular osteolipoma.

Authors:  Jin Seo Yang; Suk Hyung Kang; Yong Jun Cho; Hyuk Jai Choi
Journal:  J Korean Neurosurg Soc       Date:  2013-12-31

5.  Lumbar Intraspinal Osteolipoma Presenting as Cauda Equina Syndrome: A Case Report and Review of Literature.

Authors:  S Dilip Chand Raja; Rishi Mugesh Kanna; Ajoy Prasad Shetty; S Rajasekaran
Journal:  Case Rep Orthop       Date:  2018-10-22
  5 in total

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