Journal Article

IgG4-related hypertrophic pachymeningitis presenting with marked dural thickening, widespread white matter changes, and rectus gyrus transdiaphragmatic herniation into the sella turcica: a case report

Takai, Isamu, Hirata, Yuto, Hattori, Nobutaka, Tsutsumi, Satoshi, Hatano, Taku, Urabe, Takao, Nakahara, Toshiki, Ogawa, Takashi, Nakamura, Ryota, Yamashiro, Kazuo, Kiuchi, Reika, Watanabe, Masao

2026

Overview

IgG4-related disease is a clinically significant immune-mediated condition that can involve multiple organs. In the central nervous system, IgG4-related hypertrophic pachymeningitis is characterized by dural thickening, and the resulting mass effect may lead to various neurological deficits and characteristic imaging findings. A 54-year-old Japanese man presented with a 6-month history of slowly progressive right-sided visual impairment and visual field loss. Neurological examination revealed no abnormalities other than reduced visual acuity and visual field defects. Cranial magnetic resonance imaging revealed marked dural thickening extensively involving the bilateral frontotemporal regions, widespread frontal white matter lesions, and transdiaphragmatic herniation of the rectus gyrus into the sella turcica. The serum IgG4 level was elevated (429 mg/dL), and a dural biopsy revealed inflammatory cell infiltration with IgG4-positive plasma cells, leading to a diagnosis of IgG4-related hypertrophic pachymeningitis. Systemic evaluation, including laboratory screening and trunk computed tomography, revealed no other organ involvement apart from cervical and hilar lymphadenopathy. The patient responded well to steroid treatment (intravenous methylprednisolone followed by tapered oral prednisolone), with gradual improvement of the dural thickening, white matter lesions, rectus gyrus herniation, and visual field defects over 3 months. The serum IgG4 level decreased to 70.3 mg/dL. This case was characterized by pronounced dural thickening, widespread white matter lesions, and unprecedented rectus gyrus herniation into the sella turcica, a combination of features not previously reported. Neurologists should consider IgG4-related disease in the differential diagnosis of hypertrophic pachymeningitis accompanied by white matter lesions because early recognition and treatment may prevent irreversible neurological damage.

• Publisher: Frontiers Media SA,Frontiers Media S.A
• Subject: Acuity / Antigens / Biopsy / Blindness / Case Report / Central nervous system / Cerebrospinal fluid / Computed tomography / Differential diagnosis / Disease / Dura Mater - diagnostic imaging / Dura Mater - pathology / dural thickening / Humans / hypertrophic pachymeningitis / Hypertrophy / IgG4-related disease / Immunoglobulin G / Immunoglobulin G - blood / Immunoglobulin G - immunology / Immunoglobulin G4-Related Disease - diagnosis / Immunoglobulin G4-Related Disease - drug therapy / Lesions / Lymphadenopathy / Lymphatic system / Magnetic Resonance Imaging / Male / Meningitis - diagnosis / Meningitis - drug therapy / Meningitis - immunology / Meningitis - pathology / Methylprednisolone / Middle Aged / Neurological diseases / Paresis / Patients / Plasma cells / Prednisolone / Sella turcica (rectus gyrus transdiaphragmatic herniation) / Sella Turcica - diagnostic imaging / Sella Turcica - pathology / Steroids / Substantia alba / Visual field / Visual impairment / White Matter - diagnostic imaging / White Matter - pathology / white matter lesions