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Amyloid in bone marrow smears of patients affected by multiple myeloma
Authors:Fara Petruzziello  Pio Zeppa  Lucio Catalano  Immacolata Cozzolino  Giuseppe Gargiulo  Pellegrino Musto  Fiorella D’Auria  Vincenzo Liso  Rita Rizzi  Nadia Caruso  Catello Califano  Eugenio Piro  Maurizio Musso  Vincenza Bonanno  Antonietta Pia Falcone  Salvatore Tafuto  Francesco Di Raimondo  Michelino De Laurentiis  Fabrizio Pane  Lucio Palombini  Bruno Rotoli
Affiliation:1. Hematology, Department of Biochemistry and Medical Biotechnology, University Federico II, Naples, Italy
2. Department of Anatomopathology and Cytopathology, University Federico II, Naples, Italy
14. Department of Hematology, Federico II University, Via Pansini, 5, 80131, Naples, Italy
3. Stazione Zoologica Anton Dhorn, Naples, Italy
4. Hematology and Stem Cell Transplantation Unit, IRCCS, Rionero in Vulture, PZ, Italy
5. Hematology, AOUCP Bari, Bari, Italy
6. Hematology Unit, Annunziata Hospital, Cosenza, Italy
7. Department of Oncology and Hematology, PO Umberto I, Nocera Inferiore, Italy
8. Hematology Unit, AO Pugliese-Ciaccio, Catanzaro, Italy
9. Oncohematology Unit, Oncology Department La Maddalena, Palermo, Italy
10. Department of Hematology, IRCCS Casa Sollievo della Sofferenza, S. Giovanni Rotondo, FG, Italy
11. Oncohematology, PO S.Maria delle Grazie, Pozzuoli, Italy
12. Department of Hematology, AO Ferrarotto, Catania, Italy
13. Department of Endocrinology and Clinical Oncology, University Federico II, Naples, Italy
Abstract:Systemic AL amyloidosis is associated with nearly 15% of cases of multiple myeloma, but data on the frequency and significance of amyloid deposits in the bone marrow of patients affected by multiple myeloma without clinical signs of systemic amyloidosis are scanty. Bone marrow smears of 166 unselected patients affected by multiple myeloma (126 at diagnosis and 40 after treatment) were stained with Congo red and studied by transmission and birefringence microscopy. Both focal and diffuse storages were considered positive. Overall, 67 patients were positive and 99 were negative to Congo red and apple-green birefringence. In particular, 51 of the 126 patients studied at diagnosis and 16 of the 40 patients with advanced disease were positive. Seventeen patients were reassessed after a mean follow-up of 32 months (range: 6–91): disappearance of amyloid deposits was verified in three cases, all responsive to bortezomib-based regimens. The preliminary data available suggest that amyloid deposition in the marrow of myeloma patients is frequent, as it can be traced in nearly 40% of cases. We failed to find correlations between bone marrow amyloid deposits and immunoglobulin type, disease stage, plasma cells percentage, hemoglobin, calcium, creatinine, albumin, or β2microglobulin. Significantly higher incidence of moderate/severe peripheral neuropathy was found in patients with marrow amyloid exposed to potentially neurotoxic antineoplastic agents. Further studies and prolonged follow-up are needed to validate our findings and to define possible prognostic aspects.
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