IgG4-related hypertrophic pachymeningitis: a case report / 中华神经科杂志
Chinese Journal of Neurology
; (12): 699-704, 2023.
Article
in Zh
| WPRIM
| ID: wpr-994884
Responsible library:
WPRO
ABSTRACT
A case of IgG4-related hypertrophic pachymeningitis was reported. The patient was an elderly female, with the course of disease more than 8 years. Clinical manifestations included recurrent headache, vision and hearing loss, exophthalmos and thyroid dysfunction. Finally, she was diagnosed as IgG4-related disease and IgG4-related hypertrophic pachymeningitis by PET-CT and dural biopsy. After treatment with methylprednisolone and mycophenolate mofetil, the patient′s clinical symptoms improved.
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Index:
WPRIM
Language:
Zh
Journal:
Chinese Journal of Neurology
Year:
2023
Type:
Article