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Cystic beta2-microglobulin amyloidoma in a patient on long-term hemodialysis.

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.
AuthorsHiroaki Ogata, Fumihiko Koiwa, Junko Takahashi, Ken Takahashi, Akira Shiokawa, Takashi Kitanosono, Eriko Kinugasa, Susumu Taguchi
JournalClinical and experimental nephrology (Clin Exp Nephrol) Vol. 10 Issue 2 Pg. 159-61 (Jun 2006) ISSN: 1342-1751 [Print] Japan
PMID16791406 (Publication Type: Case Reports, Journal Article)
Chemical References
  • beta 2-Microglobulin
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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