| Literature DB >> 16791406 |
Hiroaki Ogata1, Fumihiko Koiwa, Junko Takahashi, Ken Takahashi, Akira Shiokawa, Takashi Kitanosono, Eriko Kinugasa, Susumu Taguchi.
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.Entities:
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Year: 2006 PMID: 16791406 DOI: 10.1007/s10157-006-0409-8
Source DB: PubMed Journal: Clin Exp Nephrol ISSN: 1342-1751 Impact factor: 2.617