| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8790444 | American Journal of Ophthalmology | 2018 | 14 Pages |
Abstract
Primary amyloidosis-AL is the most common form diagnosed by mass spectrometric analysis in patients with OAA. Immunohistochemistry is ineffective in the characterization of the amyloid deposits in a significant number of cases. Evaluation to exclude systemic involvement or associated underlying lymphoproliferative disorder is warranted.
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Authors
Alexander D. Blandford, Sari Yordi, Saloni Kapoor, Gabrielle Yeaney, Claudiu V. Cotta, Jason Valent, Julian D. Perry, Arun D. Singh,