OBJECTIVE: Idiopathic hypertrophic cranial pachymeningitis is a rare disease, of
undetermined pathogenesis, that is characterized by inflammation and fibrosis of the dura …

Background Idiopathic hypertrophic pachymeningitis (IHP) is a rare inflammatory disease
that causes focal or diffuse thickening of the dura mater. However, longitudinal follow up …

Background.—Idiopathic hypertrophic cranial pachymeningitis (IHCP) is an uncommon
disorder due to localized or diffuse thickening of the dura mater. While headache is the most …

Spinal idiopathic hypertrophic pachymeningitis (IHP) is a rare, chronic, nonspecific,
granulomatous inflammatory disorder of the dura with unknown etiology. It can cause a …

Idiopathic hypertrophic cranial pachymeningitis is a rare condition. A case of idiopathic
hypertrophic cranial pachymeningitis presenting as Tolosa-Hunt syndrome is being …

Hypertrophic cranial pachymeningitis (HCP) is a rare inflammatory disease of unknown
origin in which recurrence is frequently observed in spite of the initial response to steroid …

Idiopathic hypertrophic pachymeningitis (IHP) is a rare, chronic nonspecific and
granulomatous inflammatory disorder of the dura with unknown etiology. The diagnosis can …

A 42-year-old man presented with complaints of chronic daily right frontal headaches for the
past 9 months. His headaches were worse in the morning and throbbing in nature. The …

Background: Hypertrophic pachymeningitis (HPM) is a unique disorder characterized by
thickening and fibrosis of the dura mater. Clinically it presents with headache, cranial nerve …

抄録 A 51-year-old female presented with an extremely rare case of idiopathic hypertrophic
cranial pachymeningitis manifesting as markedly thickened frontotemporal meninges with …