Home Contact Sitemap

eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease multiple myeloma
Symptom C0002726|amyloidosis
Sentences 52
PubMedID- 21275130 The authors present an uncommon case of systemic amyloidosis associated with multiple myeloma in a 35-year old woman.
PubMedID- 24452148 Rapidly progressive al amyloidosis in a patient with relapsed multiple myeloma after achieving a complete response to tandem autologous pbsct.
PubMedID- 20224644 Her advanced multiple myeloma was associated with systemic amyloidosis involving gut and heart, which ultimately led to her demise.
PubMedID- 19740556 We present the case of a patient with cardiac amyloidosis due to multiple myeloma who presented with pre-syncopal episodes and intermittent brugada-like ecg pattern.
PubMedID- 21838455 A case of light chain (al) amyloidosis associated with igd multiple myeloma (mm): clinical features, laboratory findings and outcome.
PubMedID- 23420725 Association of lcdd and al amyloidosis with multiple myeloma (mm) at the time of diagnosis is common, but further progression to this condition is considered rare.
PubMedID- 21928004 Histopathological examination revealed that the patient suffered from al-type amyloidosis associated with multiple myeloma.
PubMedID- 20575017 multiple myeloma with lacrimal gland amyloidosis and sarcoidosis.
PubMedID- 21145774 Al amyloidosis with myeloma mimicking rheumatoid arthritis.
PubMedID- 22577608 In a horse with al-amyloidosis associated with multiple myeloma, diffuse severe extracellular amyloid deposits were present in the lamina propria of glandular stomach, duodenum, and jejunum.
PubMedID- 24612867 Further diagnostic work-up confirmed the diagnosis of systemic amyloidosis associated with multiple myeloma lambda light chains.
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- 20012043 However, little is known about the myeloma associated with al amyloidosis (mm/al).
PubMedID- 22241157 Systemic amyloidosis associated with igd-lambda multiple myeloma.
PubMedID- 25027215 Gastrointestinal amyloidosis in a patient with multiple myeloma.
PubMedID- 26366309 Upper gastrointestinal bleeding from gastric amyloidosis in a patient with smoldering multiple myeloma.
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- 23439244 Based on these findings, we diagnosed as al amyloidosis associated with multiple myeloma.
PubMedID- 22943012 Although incidence of other hematopoietic malignancies in the gastrointestinal tract such as plasma cell myeloma associated with amyloidosis, plasmablastic lymphoma, hodgkin disease, histiocytic sarcoma and mast cell sarcoma is extremely rare, these entities have been documented, with the latter two demonstrating aggressive clinical behavior.
PubMedID- 25221694 In addition, amyloidosis may be associated with multiple myeloma or chronic infections.
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- 22124598 We report the case of a patient with amyloidosis associated with multiple myeloma, showing clinical characteristics of pseudomyopathy.
PubMedID- 23257671 Fatal hepatic failure due to al amyloidosis in a patient with multiple myeloma.
PubMedID- 21428118 Diffuse interstitial or perivascular amyloid deposits in the lung can form in the context of systemic amyloidosis, usually associated with myeloma or monoclonal gammopathy, and less often with chronic inflammatory diseases.
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- 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- 24027647 It has been described in a few cases and when myeloma is associated with liver disease, amyloidosis, and renal disease .
PubMedID- 26050725 Gastric mucosal biopsy and general examination confirmed a diagnosis of al amyloidosis due to multiple myeloma.
PubMedID- 24406424 Al amyloidosis is associated with myeloma, and we showed recently that transthyretin-related hereditary amyloidosis was related to non-hodgkin lymphoma (nhl).
PubMedID- 21502717 Bone marrow aspiration and kidney biopsy determined that the cause of the nephrotic syndrome was renal amyloidosis due to multiple myeloma, and the patient was admitted to our department in july 2003.
PubMedID- 20697853 An unusual case of ige-multiple myeloma presenting with systemic amyloidosis 2 years after cervical plasmacytoma resection.
PubMedID- 22446653 The diagnosis of multiple myeloma associated with primary amyloidosis in a patient with terminal renal failure, was reached.
PubMedID- 21816711 Kidney failure in patients with presumed multiple myeloma also may result from amyloidosis, light chain deposition disease, or acute tubular necrosis caused by nephrotoxic agents; therefore, identification of patients at risk for kidney damage is essential.
PubMedID- 24179667 A 64-year-old female was diagnosed with systemic amyloidosis associated with multiple myeloma.
PubMedID- 22008141 The occurrence of systemic amyloidosis in myeloma is well documented, but the osseous location is rare and rarely revealed.
PubMedID- 24913114 In polish studies, there are no statistics and analyses of the factors that may influence the development of amyloidosis in patients with multiple myeloma.
PubMedID- 20470479 Discussion: primary amyloidosis associated with light chain myeloma is a rare, and often late, diagnosis with a dismal prognosis.
PubMedID- 25437571 Meticulous and appropriate treatment for severe complications involving amyloidosis associated with multiple myeloma can prevent a fatal outcome.
PubMedID- 23569501 Al type amyloidosis may develop 15% of cases of multiple myeloma .
PubMedID- 26113598 myeloma, kappa-light chain, with light-chain amyloidosis was diagnosed.
PubMedID- 25011639 Further investigation revealed that the patient had amyloid light-chain type amyloidosis due to multiple myeloma.
PubMedID- 26522192 amyloidosis with multiple myeloma presenting with acromegalic features.
PubMedID- 22993476 1 conjunctival involvement in amyloidosis associated with myeloma presents as subconjunctival hemorrhage presumably due to amyloid deposits in the walls of small vessels causing fragility.
PubMedID- 22481660 Primary systemic amyloidosis associated with multiple myeloma.
PubMedID- 25803181 We report a case of multiple myeloma-associated light-chain amyloidosis with severe cardiac involvement presenting with acute and rapidly deteriorating heart failure where full evaluation was not possible and in whom death would occur without ecmo support.
PubMedID- 25140565 11c-pib pet/ct in nasopharyngeal amyloidosis associated with 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.
PubMedID- 20561488 The diagnosis of generalised amyloidosis in association with multiple myeloma with cardiac and renal involvement was established.
PubMedID- 23788103 Triple-trouble cardiomyopathy: myocardial infarction, diastolic heart failure, and conduction defects due to amyloidosis associated with multiple myeloma.
PubMedID- 22363889 Moreover, multiple myeloma has been associated with cardiac amyloidosis which can exacerbate the heart failure that might already be present in patients with diabetes mellitus .

Page: 1 2