Spinal Langerhans cell histiocytosis with cord compression and neurological deficits: A case report
- PMID: 37269759
- PMCID: PMC10248222
- DOI: 10.1016/j.ijscr.2023.108351
Spinal Langerhans cell histiocytosis with cord compression and neurological deficits: A case report
Abstract
Introduction and importance: Langerhans cell histiocytosis (LCH) is a rare idiopathic disease that uncommonly affect the spine in adults.
Case presentation: In this report, we presented a rare adult case of symptomatic spinal LCH with asymptomatic systemic involvement. She was a 46-year-old previously healthy lady who presented with subacute thoracic sensory level, urine retention, constipation, and pyramidal paraplegia. Her magnetic resonance imaging (MRI) of the spine revealed T6 compression fracture with an epidural mass compressing the cord.
Clinical discussion: Sellar MRI showed pituitary gland enlargement with hyperintense signal in the posterior lobe. Positron emission tomography (PET)/computed tomography (CT) scan showed an increased uptake in the right parotid gland uptake and renal cortex, indicating systemic involvement.
Conclusion: Surgical excision, decompression, and screw fixation were performed, and the patient improved. The prognosis is usually good in patients with solitary spinal LCH.
Keywords: Histiocytosis; Langerhans cell histiocytosis; Spinal cord.
Copyright © 2023 The Authors. Published by Elsevier Ltd.. All rights reserved.
Conflict of interest statement
Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
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