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Idiopathic Hypertrophic Spinal Pachymeningitis with Spinal Cord Lesion: A Case Report

Idiopathic hypertrophic spinal pachymeningitis (IHSP) is a rare, diffuse inflammatory fibrosis of the dura mater that can lead to spinal cord compression. Though the optimal treatment is controversial, some reports recommend decompressive surgery and postoperative steroid therapy. However, we encoun...

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Autores principales: Park, Jae yeon, Choi, Il, Khil, Eun Kyung, Kim, Wu Jae, Shin, Il Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Neurotraumatology Society 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7607016/
https://www.ncbi.nlm.nih.gov/pubmed/33163452
http://dx.doi.org/10.13004/kjnt.2020.16.e17
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author Park, Jae yeon
Choi, Il
Khil, Eun Kyung
Kim, Wu Jae
Shin, Il Young
author_facet Park, Jae yeon
Choi, Il
Khil, Eun Kyung
Kim, Wu Jae
Shin, Il Young
author_sort Park, Jae yeon
collection PubMed
description Idiopathic hypertrophic spinal pachymeningitis (IHSP) is a rare, diffuse inflammatory fibrosis of the dura mater that can lead to spinal cord compression. Though the optimal treatment is controversial, some reports recommend decompressive surgery and postoperative steroid therapy. However, we encountered a case of pachymeningitis that worsened after decompressive surgery. A 79-year-old woman presented with gait disturbance and bilateral lower extremity weakness that began 6 months prior. She had radiating pain on the C5 and T1 dermatomes and clumsiness in both hands. Magnetic resonance imaging (MRI) revealed diffuse thickening of the posterior longitudinal ligament of C6 to T4/5 and ligamentum flavum of C3/4 to T4/5, causing central canal stenosis and compressive myelopathy. She underwent posterior decompressive laminectomy from C4 to T1 total (T2 subtotal) and cervicothoracic screw fixation. During surgery, we found severe adhesion of the posterior longitudinal ligament and ligamentum flavum to the dura mater. Chronic inflammation with fibrosis and lymphoplasmacytic infiltration were present. After surgery, the patient's motor weakness worsened. Despite steroid treatment, her symptom severity fluctuated. Follow-up MRI obtained 3 months postoperation revealed high signal intensity from C5 to T2, possibly indicating aggravated compressive myelopathy. Thus, in this case, decompressive surgery and steroid therapy were detrimental.
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spelling pubmed-76070162020-11-05 Idiopathic Hypertrophic Spinal Pachymeningitis with Spinal Cord Lesion: A Case Report Park, Jae yeon Choi, Il Khil, Eun Kyung Kim, Wu Jae Shin, Il Young Korean J Neurotrauma Case Report Idiopathic hypertrophic spinal pachymeningitis (IHSP) is a rare, diffuse inflammatory fibrosis of the dura mater that can lead to spinal cord compression. Though the optimal treatment is controversial, some reports recommend decompressive surgery and postoperative steroid therapy. However, we encountered a case of pachymeningitis that worsened after decompressive surgery. A 79-year-old woman presented with gait disturbance and bilateral lower extremity weakness that began 6 months prior. She had radiating pain on the C5 and T1 dermatomes and clumsiness in both hands. Magnetic resonance imaging (MRI) revealed diffuse thickening of the posterior longitudinal ligament of C6 to T4/5 and ligamentum flavum of C3/4 to T4/5, causing central canal stenosis and compressive myelopathy. She underwent posterior decompressive laminectomy from C4 to T1 total (T2 subtotal) and cervicothoracic screw fixation. During surgery, we found severe adhesion of the posterior longitudinal ligament and ligamentum flavum to the dura mater. Chronic inflammation with fibrosis and lymphoplasmacytic infiltration were present. After surgery, the patient's motor weakness worsened. Despite steroid treatment, her symptom severity fluctuated. Follow-up MRI obtained 3 months postoperation revealed high signal intensity from C5 to T2, possibly indicating aggravated compressive myelopathy. Thus, in this case, decompressive surgery and steroid therapy were detrimental. Korean Neurotraumatology Society 2020-06-05 /pmc/articles/PMC7607016/ /pubmed/33163452 http://dx.doi.org/10.13004/kjnt.2020.16.e17 Text en Copyright © 2020 Korean Neurotraumatology Society https://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Park, Jae yeon
Choi, Il
Khil, Eun Kyung
Kim, Wu Jae
Shin, Il Young
Idiopathic Hypertrophic Spinal Pachymeningitis with Spinal Cord Lesion: A Case Report
title Idiopathic Hypertrophic Spinal Pachymeningitis with Spinal Cord Lesion: A Case Report
title_full Idiopathic Hypertrophic Spinal Pachymeningitis with Spinal Cord Lesion: A Case Report
title_fullStr Idiopathic Hypertrophic Spinal Pachymeningitis with Spinal Cord Lesion: A Case Report
title_full_unstemmed Idiopathic Hypertrophic Spinal Pachymeningitis with Spinal Cord Lesion: A Case Report
title_short Idiopathic Hypertrophic Spinal Pachymeningitis with Spinal Cord Lesion: A Case Report
title_sort idiopathic hypertrophic spinal pachymeningitis with spinal cord lesion: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7607016/
https://www.ncbi.nlm.nih.gov/pubmed/33163452
http://dx.doi.org/10.13004/kjnt.2020.16.e17
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