A case report of idiopathic hypertrophic pachymeningitis
Idiopathic hypertrophic pachymeningitis (IHP) is a condition characterised by diffuse or local thickening and fibrosis of dura matter caused by inflammation of unknown origin. It is a diagnosis of exclusion. Autoimmune disorders (notably ANCA-associated vasculitis (AAV) and IgG4-related disease) po...
Saved in:
Main Authors: | G. Makarevičius, J. Grigaitė, M. Jokubaitis, A. Klimašauskienė |
---|---|
Format: | Article |
Language: | English |
Published: |
Vilnius University Press
2022-03-01
|
Series: | Neurologijos seminarai |
Subjects: | |
Online Access: | https://www.journals.vu.lt/neurologijos_seminarai/article/view/29291 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Differential diagnosis of hypertrophic pachymeningitis: literature review
by: G. Makarevičius, et al.
Published: (2022-03-01) -
Human T follicular helper cells and their impact on IgE and IgG4 production across allergy, malignancy, and IgG4-related disease
by: Mitsuhiro Akiyama, et al.
Published: (2025-01-01) -
Research Progress of Perioperative Anesthesia Management in Patients with Hypertrophic Cardiomyopathy
by: LIN Shuantong, et al.
Published: (2025-01-01) -
Hypertrophic cardiomyopathy with mid-ventricular obstruction and apical aneurysm
by: N.D. Oryshchyn, et al.
Published: (2016-11-01) -
Cardiac Amyloidosis Masquerading as Hypertrophic Obstructive Cardiomyopathy: Co-existence or Coincidence?
by: Madhu Shukla, et al.
Published: (2024-07-01)