Abstract |
A 72-year-old woman with Mikulicz disease with pathogically proven sclerosing sialadenitis showed systemic abnormal F-18 FDG uptake in the bilateral lacrimal and submandibular glands, pancreas, abdominal aortic wall, and a retroperitoneal fibroid mass on PET/CT scan, with marked elevation of the serum IgG4 level. This case supports Mikulicz disease being included as 1 of the disorders associated with a new clinical entity of systemic IgG4-related plasmacytic syndrome. A whole-body FDG-PET/CT scan can be expected as a useful tool for detecting systemic involvement in systemic IgG4-related plasmacytic syndrome.
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Authors | Kazuyoshi Suga, Yasuhiko Kawakami, Atsuto Hiyama, Kenji Hori, Megumi Takeuchi |
Journal | Clinical nuclear medicine
(Clin Nucl Med)
Vol. 34
Issue 3
Pg. 164-7
(Mar 2009)
ISSN: 1536-0229 [Electronic] United States |
PMID | 19352281
(Publication Type: Case Reports, Journal Article)
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Chemical References |
- Immunoglobulin G
- Fluorodeoxyglucose F18
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Topics |
- Aged
- Female
- Fluorodeoxyglucose F18
(metabolism)
- Humans
- Immunoglobulin G
(blood)
- Mikulicz' Disease
(blood, diagnostic imaging, pathology)
- Plasma Cells
(diagnostic imaging, pathology)
- Positron-Emission Tomography
- Tomography, X-Ray Computed
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