Abstract | BACKGROUND: CASE DESCRIPTION: We report a case of a 62-year-old man who presented with visual disturbance and quadrantanopia of the right eye. Magnetic resonance imaging revealed uniformly enhancing masses located near the right paraclinoid at the right Meckel's cave and along the left foramen magnum. He had experienced autoimmune pancreatitis 7 years previously, and the condition had responded to steroid therapy. Laboratory data revealed elevation of IgG (1877 mg/dL) and IgG4 (405 ng/dL). The right paraclinoidal lesion causing visual disturbance was subtotally removed, which provided sufficient decompression of the right optic nerve. IgG4 was strongly positive on immunohistochemical staining, and we started oral corticosteroid medication. Consequently, all lesion masses shrank remarkably within 1 month. CONCLUSION: There have been a growing number of reports of such multiple pseudotumors associated with IgG4-related disease. In differential diagnosis, this disease entity requires special attention when multiple dural-based tumors are observed. Preoperative presumption is very important because this disease is likely to respond to steroid therapy.
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Authors | Atsushi Okano, Hirofumi Nakatomi, Junji Shibahara, Tsukasa Tsuchiya, Nobuhito Saito |
Journal | World neurosurgery
(World Neurosurg)
Vol. 83
Issue 6
Pg. 1181.e1-4
(Jun 2015)
ISSN: 1878-8769 [Electronic] United States |
PMID | 25725165
(Publication Type: Case Reports, Journal Article, Review)
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Copyright | Copyright © 2015 Elsevier Inc. All rights reserved. |
Chemical References |
- Adrenal Cortex Hormones
- Immunoglobulin G
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Topics |
- Adrenal Cortex Hormones
(therapeutic use)
- Autoimmunity
- Diagnosis, Differential
- Granuloma, Plasma Cell
(complications, diagnosis, drug therapy)
- Humans
- Immunoglobulin G
(blood)
- Male
- Meningeal Neoplasms
(diagnosis)
- Meningioma
(diagnosis)
- Middle Aged
- Pancreatitis
(immunology)
- Pseudotumor Cerebri
(complications, diagnosis, drug therapy)
- Treatment Outcome
- Vision Disorders
(etiology)
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