| Literature DB >> 26753903 |
Nishanth Sadashiva1, P Rajalakshmi2, Anita Mahadevan2, Vikas Vazhayil1, Kannepalli Narasinga Rao3, Sampath Somanna1.
Abstract
INTRODUCTION: Langerhans cell histiocytosis (LCH) is a rare condition, and even rare is cervical spine involvement. CASE REPORT: A 9-year-old girl had neck pain, neck tilt and left upper limb weakness, occasional fever and positive family history of tuberculosis. Imaging showed C5 vertebral body collapse with epidural and prevertebral soft tissue collection causing cord and nerve root compression. The patient underwent C5 corpectomy and fusion. Histopathological was suggestive of LCH. She underwent radiotherapy and was asymptomatic at 1-year follow-up.Entities:
Keywords: Eosinophilic granulomas; Hand-Schüller-Christian disease; Langerhans cell granulomatosis; Letterer-Siwe disease
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Year: 2016 PMID: 26753903 DOI: 10.1007/s00381-015-2989-7
Source DB: PubMed Journal: Childs Nerv Syst ISSN: 0256-7040 Impact factor: 1.475