医学
外科
弱点
强的松
组织病理学
脑膜
软组织
病理
作者
MenaG Kerolus,David L. Kramer,Karina Furlan,Sukriti Nag,John O’Toole
出处
期刊:Neurology India
[Medknow Publications]
日期:2022-01-01
卷期号:70 (3): 1180-1180
被引量:2
标识
DOI:10.4103/0028-3886.349607
摘要
IgG4-related disease is a rare, recently recognized chronic inflammatory disease. IgG4-related hypertrophic pachymeningitis (IgG4-RHP) of the central nervous system predominantly involves the cranial meninges. Spinal involvement remains rare.We report a case of recurrent cervicothoracic IgG4-RHP and review the surgical literature.A 35-year-old woman presented with a 6-month history of neck and right shoulder pain, progressive right triceps weakness and paresthesias in the right C8 and T1 dermatomes. MRI demonstrated a T2 hypointense epidural soft tissue mass extending from C6-T1. The patient underwent C6-T1 laminoforaminotomy and partial resection with near complete symptom resolution. Histopathology was consistent with diagnosis of IgG4-RHP. Eighteen months postoperatively, she experienced symptom recurrence necessitating re-operation and adjuvant postoperative prednisone with complete resolution at 40-months' follow-up.Of the now nineteen confirmed cases of IgG4-RHP, fifteen underwent surgery. A majority achieved partial resection. Three surgical patients did not receive adjuvant therapy with symptomatic recurrence between 2 and 18 months.
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