Abstract |
We report a patient with beta2 microglobulin amyloidosis (beta2M) in whom cystic tumors were seen in the bilateral axillary region. The patient was a 68-year-old woman who had been on hemodialysis for more than 20 years because of IgA nephropathy. Computed tomography-guided biopsy was performed to confirm the diagnosis. Congo red staining, beta2M immunohistochemistry, and electron microscopy examination of the biopsied sample showed extended beta2M deposits in the cystic tumor. beta2M-related amyloidosis in patients with long-term dialysis commonly presents as osteoarticular disease, although a soft-tissue pseudotumor, known as amyloidoma, has been reported. This is the first report in the English-language literature of amyloidosis presenting as bilateral axillary cystic tumors.
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Authors | Hiroaki Ogata, Fumihiko Koiwa, Junko Takahashi, Ken Takahashi, Akira Shiokawa, Takashi Kitanosono, Eriko Kinugasa, Susumu Taguchi |
Journal | Clinical and experimental nephrology
(Clin Exp Nephrol)
Vol. 10
Issue 2
Pg. 159-61
(Jun 2006)
ISSN: 1342-1751 [Print] Japan |
PMID | 16791406
(Publication Type: Case Reports, Journal Article)
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Chemical References |
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Topics |
- Aged
- Amyloidosis
(etiology, pathology)
- Axilla
(pathology)
- Cysts
(etiology)
- Female
- Glomerulonephritis, IGA
(therapy)
- Humans
- Renal Dialysis
(adverse effects)
- beta 2-Microglobulin
(immunology)
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