Idiopathic hypertrophic pachymeningitis: A case report and review of the literature

Abstract

We report the treatment and follow-up, including magnetic resonance imaging (MRI) of a patient with idiopathic hypertrophic pachymeningitis and review the literature published in 21th century, with emphasis on the management and clinical outcomes of this rare disorder. Hypertrophic pachymeningitis is extremely rare. It is a fibrosing inflammatory process which involves the dura mater. Numerous pathological entities produce thickening of the pachymeninges. Thus, idiopathic hypertrophic pachymeningitis is diagnosed by exclusion. We present a case of patient with idiopathic hypertrophic pachymeningitis who had varied clinical presentation. Imaging studies revealed diffuse thickening of the pachymeninges.

Authors and Affiliations

Anahita zoghi| Assistant Professor of Neurology Shahid Beheshti University of Medical Science Loghman Hakim Hospital, Iran, Navid Rahimi| MD Rheumatology Fellowship Iran University of Medical Science (IUMS) Hazrat Rasool General Hospital, Iran, Corresponding email: dr.navid57@gmail.com, Shervin shokouhi| Associate Professor of Infectious Disease Shahid Beheshti University of Medical Science Loghman Hakim Hospital, Iran, Ehsan sakhaee| MD Neurology Resident Shahid Beheshti University of Medical Science Loghman Hakim Hospital, Iran

Keywords

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  • EP ID EP11630
  • DOI -
  • Views 242
  • Downloads 10

How To Cite

Anahita zoghi, Navid Rahimi, Shervin shokouhi, Ehsan sakhaee (2016). Idiopathic hypertrophic pachymeningitis: A case report and review of the literature. International Journal of Medical Research & Health Sciences (IJMRHS), 5(4), 190-197. https://europub.co.uk/articles/-A-11630