Teaching NeuroImages: Idiopathic hypertrophic spinal pachymeningitis mimicking epidural lymphoma.
نویسندگان
چکیده
A 41-year-old man presented with bilateral leg numbness and paraparesis for 3 months. MRI showed a circumferential long epidural mass extending from T2 to T4 level (figure 1). Histologic examination demonstrated dense fibrous tissue with inflammatory infiltrate (figure 2). By exclusion of trauma, infectious diseases, and autoimmune diseases, idiopathic hypertrophic spinal pachymeningitis (IHSP) was diagnosed. IHSP is a rare inflammatory disease characterized by hypertrophic inflammation of the dura mater. The typical MRI finding of IHSP is a long epidural mass of low T2 signal intensity with peripheral enhancement. Homogeneous enhancement is typical of and could be mistaken for epidural lymphoma.
منابع مشابه
Idiopathic Hypertrophic Spinal Pachymeningitis: A Rare Entity
We describe a case of idiopathic hypertrophic spinal pachymeningitis in a 62 -year -old gentleman presenting with progressive myelopathy of two years. The imaging and corresponding histological findings are discussed and correlated.
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متن کاملTeaching NeuroImage: idiopathic hypertrophic spinal pachymeningitis.
A 42-year-old woman had progressive numbness from both feet to mid chest for 2 weeks. Examination showed a sensory level at T8, no weakness, and brisk reflexes throughout. MRI showed T2–T5 dural thickening (figure 1). Testing revealed an elevated sedimentation rate and normal chest x-ray, CSF analyses, and tests for rheumatologic diseases and infections. Dural biopsy showed an inflammatory infi...
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عنوان ژورنال:
- Neurology
دوره 84 9 شماره
صفحات -
تاریخ انتشار 2015