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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease amyloidosis
Symptom C0026764|multiple myeloma
Sentences 28
PubMedID- 24913114 The occurrence of al amyloidosis (light-chain amyloidosis) in patients with multiple myeloma in lower silesia region, poland.
PubMedID- 25437571 Pathological findings suggested that the causative factor was amyloidosis with multiple myeloma.
PubMedID- 21927567 To date, there has only been a few case reports that have described primary amyloidosis associated with multiple myeloma and this resulted in subacute or acute, fulminant hepatic failure (3-5).
PubMedID- 24452148 Rapidly progressive al amyloidosis in a patient with relapsed multiple myeloma after achieving a complete response to tandem autologous pbsct.
PubMedID- 25210137 One such example is al amyloidosis associated with multiple myeloma, in which overproduced immunoglobulin light chains get deposited onto tissues, leading to tissue dysfunction.
PubMedID- 22124598 We report the case of a patient with amyloidosis associated with multiple myeloma, showing clinical characteristics of pseudomyopathy.
PubMedID- 22512230 The patient had been diagnosed with multiple myeloma associated with light-chain amyloidosis after biopsy of the gastric mucosa and bone marrow aspirate.
PubMedID- 20224644 Her advanced multiple myeloma was associated with systemic amyloidosis involving gut and heart, which ultimately led to her demise.
PubMedID- 21883489 Eleven patients had systemic involvement by amyloidosis (associated either with multiple myeloma or plasma cell dyscrasia/monoclonal gammopathies), while three presented the localized type, one of them associated with plasmacytoma.
PubMedID- 22577608 Clinical signs including rapid weight loss, muscle atrophy, soft unformed stool, and ventral edema were noted in a case of a horse gelding with al amyloidosis associated with multiple myeloma .
PubMedID- 22446653 The diagnosis of multiple myeloma associated with primary amyloidosis in a patient with terminal renal failure, was reached.
PubMedID- 23257671 Fatal hepatic failure due to al amyloidosis in a patient with multiple myeloma.
PubMedID- 21928004 Histopathological examination revealed that the patient suffered from al-type amyloidosis associated with multiple myeloma.
PubMedID- 22241157 Systemic amyloidosis associated with igd-lambda multiple myeloma.
PubMedID- 25140565 11c-pib pet/ct in nasopharyngeal amyloidosis associated with multiple myeloma.
PubMedID- 25027215 Gastrointestinal amyloidosis in a patient with multiple myeloma.
PubMedID- 20561488 The diagnosis of generalised amyloidosis in association with multiple myeloma with cardiac and renal involvement was established.
PubMedID- 20575017 multiple myeloma with lacrimal gland amyloidosis and sarcoidosis.
PubMedID- 24250091 1 amyloidosis in multiple myeloma is characterized by the elaboration of excess light chains by the host.
PubMedID- 24179667 A 64-year-old female was diagnosed with systemic amyloidosis associated with multiple myeloma.
PubMedID- 22481660 Primary systemic amyloidosis associated with multiple myeloma.
PubMedID- 20697853 An unusual case of ige-multiple myeloma presenting with systemic amyloidosis 2 years after cervical plasmacytoma resection.
PubMedID- 25221694 In addition, amyloidosis may be associated with multiple myeloma or chronic infections.
PubMedID- 25275414 We present a case of a primary systemic amyloidosis associated with multiple myeloma in a 48-year-old woman whose tc-mdp spect/ct study revealed extraosseous periarticular uptake in amyloid deposits with no abnormal focal tracer uptake in the bone.
PubMedID- 23788103 Triple-trouble cardiomyopathy: myocardial infarction, diastolic heart failure, and conduction defects due to amyloidosis associated with multiple myeloma.
PubMedID- 23439244 Based on these findings, we diagnosed as al amyloidosis associated with multiple myeloma.
PubMedID- 26366309 Upper gastrointestinal bleeding from gastric amyloidosis in a patient with smoldering multiple myeloma.
PubMedID- 22909024 Most patients have evidence of isolated monoclonal gammopathy or smoldering myeloma, and the occurrence of al amyloidosis in patients with symptomatic multiple myeloma or other b-cell lymphoproliferative disorders is unusual.

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