A 43-year-old man presented with severe heart failure secondary to high-risk light chain cardiac amyloidosis. He underwent chemotherapy and autologous stem cell transplantation with complete hematologic response. Serial cardiac magnetic resonance imaging post-transplant demonstrated gradual normalization of biventricular function and myocardial T1, a surrogate measure of disease burden
A 77-year-old man visited our hospital complaining of aggravated exertional chest pain. He was diagn...
Abstract INTRODUCTION: Amyloidosis is a systemic disease. Heart transplantation in this subset of p...
It is known that the prognosis of patients affected by light-chain (AL) or transthyretin-related (TT...
AbstractOur report describes a case of 57-year-old man with manifest heart failure on the basis of c...
AL amyloidosis and multiple myeloma result in extracellular deposition of insoluble fibrillary prote...
Background: AL amyloidosis and multiple myeloma result in extracellular deposition of insoluble fibr...
A 55-year-old woman presented with progressive heartfailure symptoms and was diagnosed by endomyocar...
Background: AL amyloidosis and multiple myeloma result in extracellular deposition of insoluble fibr...
International audienceSimultaneous cardiac and renal involvement is associated with a particularly p...
International audienceWe report the case of a 62-year-old man hospitalized in May 2015 for symptomat...
International audienceRecurrence in the allograft and progression in other organs increase mortality...
SummaryBackgroundImmunoglobulinic (AL) amyloidosis is a complication of plasma cell dyscrasia, chara...
International audienceBACKGROUND: Immunoglobulinic (AL) amyloidosis is a complication of plasma cell...
Amyloidosis is a multisystemic disease characterized by the accumulation of abnormal proteins in ext...
Cardiac transplantation is currently the only established surgical approach to the treatment of refr...
A 77-year-old man visited our hospital complaining of aggravated exertional chest pain. He was diagn...
Abstract INTRODUCTION: Amyloidosis is a systemic disease. Heart transplantation in this subset of p...
It is known that the prognosis of patients affected by light-chain (AL) or transthyretin-related (TT...
AbstractOur report describes a case of 57-year-old man with manifest heart failure on the basis of c...
AL amyloidosis and multiple myeloma result in extracellular deposition of insoluble fibrillary prote...
Background: AL amyloidosis and multiple myeloma result in extracellular deposition of insoluble fibr...
A 55-year-old woman presented with progressive heartfailure symptoms and was diagnosed by endomyocar...
Background: AL amyloidosis and multiple myeloma result in extracellular deposition of insoluble fibr...
International audienceSimultaneous cardiac and renal involvement is associated with a particularly p...
International audienceWe report the case of a 62-year-old man hospitalized in May 2015 for symptomat...
International audienceRecurrence in the allograft and progression in other organs increase mortality...
SummaryBackgroundImmunoglobulinic (AL) amyloidosis is a complication of plasma cell dyscrasia, chara...
International audienceBACKGROUND: Immunoglobulinic (AL) amyloidosis is a complication of plasma cell...
Amyloidosis is a multisystemic disease characterized by the accumulation of abnormal proteins in ext...
Cardiac transplantation is currently the only established surgical approach to the treatment of refr...
A 77-year-old man visited our hospital complaining of aggravated exertional chest pain. He was diagn...
Abstract INTRODUCTION: Amyloidosis is a systemic disease. Heart transplantation in this subset of p...
It is known that the prognosis of patients affected by light-chain (AL) or transthyretin-related (TT...