PedAM
Pediatric Disease Annotations & Medicines
| Disease | amyloidosis |
| Phenotype | C1136084|plasma cell dyscrasia |
| Sentences | 9 |
| PubMedID- 22289269 | Al amyloidosis results from plasma cell dyscrasia that produces monoclonal light-chain igs, whose fragments deposit as this protein. |
| PubMedID- 21954412 | Al amyloidosis has been associated with plasma cell dyscrasias, such as, multiple myeloma. |
| PubMedID- 25852856 | Ig-related amyloidosis is associated with plasma cell dyscrasias and can rarely be seen with other lymphoproliferative disorders. |
| PubMedID- 25173210 | We report 2 cases of amyloidosis associated with plasma cell dyscrasia. |
| PubMedID- 22542865 | Hence, primary amyloidosis is associated with plasma cell dyscrasias, namely multiple myeloma and waldenström macroglobulinemia/lymphoplasmacytic lymphoma[2,4]. |
| PubMedID- 21883489 | Conclusions: our results show that the head and neck region is preferentially affected by systemic al-amyloidosis, usually associated with plasma cell dyscrasia. |
| PubMedID- 21927567 | Hepatic involvement is common in systemic amyloidosis and in patients with b-cell and plasma cell dyscrasia. |
| PubMedID- 21603298 | The primary amyloidosis has been associated with a monoclonal plasma cell dyscrasia, as at least 30% of those patients will eventually progress to multiple myeloma. |
| PubMedID- 24959390 | We present a relatively uncommon cause of heart disease, cardiac amyloidosis in a patient with a systemic plasma cell dyscrasia, and multiple myeloma. |
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