Cystic [beta]2-microglobulin amyloidoma in a patient on long-term hemodialysis

We report a patient with β2 microglobulin amyloidosis (β2M) 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...

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Veröffentlicht in:Clinical and experimental nephrology 2006-06, Vol.10 (2), p.159
Hauptverfasser: Ogata, Hiroaki, Koiwa, Fumihiko, Takahashi, Junko, Takahashi, Ken, Shiokawa, Akira, Kitanosono, Takashi, Kinugasa, Eriko, Taguchi, Susumu
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Sprache:eng
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Zusammenfassung:We report a patient with β2 microglobulin amyloidosis (β2M) 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, β2M immunohistochemistry, and electron microscopy examination of the biopsied sample showed extended β2M deposits in the cystic tumor. β2M-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.
ISSN:1342-1751
1437-7799
DOI:10.1007/s10157-006-0409-8