These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Search MEDLINE/PubMed

  • Title: Primary myoepithelioma of the dorsal spine: a case report and review of literature.
    Author: Savardekar AR, Goudihalli S, Chatterjee D, Ahuja CK, Salunke P.
    Journal: Spine (Phila Pa 1976); 2014 Nov 15; 39(24):E1488-92. PubMed ID: 25188604.
    Abstract:
    STUDY DESIGN: Case report and review of the relevant literature. OBJECTIVE: To present a case of primary spinal myoepithelioma and discuss its clinical, radiological and histopathological characteristics. We report a long-term follow-up of 5 years. SUMMARY OF BACKGROUND DATA: Myoepithelial neoplasms, represent a diverse morphological and biological spectrum of tumors, composed of epithelial and myoepithelial elements. Primary myoepithelioma of the bone is extremely rare and very few cases of spinal myoepitheliomas have been reported till date. METHODS: A 50-year male, presenting with complaints of paraparesis and difficulty in walking, was diagnosed to have an expansile lytic lesion involving the D10 vertebral body with paraspinal extension. The patient underwent D10 laminectomy and gross total resection of the tumor. Patient's power improved postoperatively, and he returned to his full functional status. RESULTS: Long-term follow-up of 5 years reveals 2 recurrences, despite gross total resection at the initial surgery followed by radiotherapy. Histopathology, at the third surgery, documents the transformation of myoepithelioma into myoepithelial carcinoma. CONCLUSION: Primary myoepithelioma of spine is very rare. Gross total resection with wide resection margins in the paraspinal region should be used to tackle this rare entity as the role of adjuvant therapy is doubtful. Long-term follow-up is a must.
    [Abstract] [Full Text] [Related] [New Search]