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An Unusual Presentation of a Cervical Paraspinal Leiomyoma in an Adolescent Female.

Authors :
Swarz, Jeffrey A.
Anilkumar, Arayamparambil C.
Miller, Douglas C.
Litofsky, N. Scott
Tanaka, Tomoko
Source :
Pediatric & Developmental Pathology; May/Jun2018, Vol. 21 Issue 3, p335-340, 6p
Publication Year :
2018

Abstract

Objective We describe an apparently unique case of an extra-uterine leiomyoma in the cervical paraspinal tissue including its evaluation and management. Methods A 14-year-old girl was referred to the neurology clinic for an abnormal head CT following a concussion. MRI revealed a homogenously enhancing left cervical paraspinal mass. The patient underwent complete resection and subsequent genetic testing and counseling were obtained to determine the presence of Li–Fraumeni Syndrome (LFS) or Hereditary Leiomyomatosis and Renal Cell Cancer (HLRCC) mutations. Result Histopathological examination proved that the tumor was a benign leiomyoma. Genomic testing for Fumarate Hydratase Gene, HLRCC, TP53 mutations or deletions, and LFS sequencing were negative. Further testing showed no immunosuppression. Conclusions To the best of our knowledge, this is the only case of paraspinal leiomyoma to have been reported to date. We emphasize the importance of considering immunosuppression, LFS, or HLRCC as an underlying cause in extra-uterine leiomyata. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10935266
Volume :
21
Issue :
3
Database :
Complementary Index
Journal :
Pediatric & Developmental Pathology
Publication Type :
Academic Journal
Accession number :
130022935
Full Text :
https://doi.org/10.1177/1093526617706815