The authors present an uncommon case of systemic amyloidosis associated with multiple myeloma in a 35-year old woman. Systemic amyloidosis commonly presents in association with clonal plasma cell proliferative disorders, and less frequently as secondary or of a hereditary origin. Amyloidosis is usually associated with multiple myeloma in older patients and frequently has an unfavourable prognosis. Keywords: Amyloidosis, multiple myeloma "Amiloidosis de Cadenas Ligeras de Asociada con Mieloma Múltiple en un Paciente Joven: Reporte de un Caso" RESUMEN Los autores presentan aquí un caso raro de amiloidosis sistémica asociado con mieloma múltiple en una mujer de 35 años de edad. La amiloidosis sistémica nor...
Multiple myeloma (MM) is an immunoglobulin-producing tumor of plasma cells, which occurs commonly in...
International audienceIntroductionAL amyloidosis is caused by the proliferation of an immunoglobulin...
Amyloidosis is a systemic illness characterized by the extracellular deposition of abnormal proteins...
Introduction: Primary systemic amyloidosis is part of the spectrum of plasma cell neoplasms, in whic...
The clinical spectrum of plasma cell dyscrasias includes primary amyloidosis and multiple myeloma. T...
This case report is about a 48-year-old female patient with systemic amyloidosis and multiple myelom...
We report a case of multiple myeloma associated with light-chain amyloidosis in a 62-year old woman....
Amyloidosis is a disease of unknown cause, characterized by the accumulation of amorphous protein ma...
Multiple myeloma, being a malignant proliferation of plasma cells in the bone marrow, has clinical s...
Amyloid light chain (AL) amyloidosis and multiple myeloma (MM) are both clonal plasma cell disorders...
International audienceUNLABELLED: DEFINITION OF THE DISEASE: AL amyloidosis results from extra-cellu...
The diagnosis of primary systemic amyloidosis, also known as AL (amyloid light-chain) amyloidosis, i...
Amyloidosis is a rare disease that is often seen in conjunction with multiple myeloma (MM). Its dama...
报告1例原发性系统性淀粉样变性并发多发性骨髓瘤.患者男,68岁.表现为紫癜、瘀斑、斑块的原发性系统性淀粉样变性,患者曾被多次误诊,最终确诊为原发性系统性淀粉样变性并发多发性骨髓瘤.中文核心期刊要目总览...
Immunoglobulin light chain (AL) amyloidosis is a systemic disease in which different systems such as...
Multiple myeloma (MM) is an immunoglobulin-producing tumor of plasma cells, which occurs commonly in...
International audienceIntroductionAL amyloidosis is caused by the proliferation of an immunoglobulin...
Amyloidosis is a systemic illness characterized by the extracellular deposition of abnormal proteins...
Introduction: Primary systemic amyloidosis is part of the spectrum of plasma cell neoplasms, in whic...
The clinical spectrum of plasma cell dyscrasias includes primary amyloidosis and multiple myeloma. T...
This case report is about a 48-year-old female patient with systemic amyloidosis and multiple myelom...
We report a case of multiple myeloma associated with light-chain amyloidosis in a 62-year old woman....
Amyloidosis is a disease of unknown cause, characterized by the accumulation of amorphous protein ma...
Multiple myeloma, being a malignant proliferation of plasma cells in the bone marrow, has clinical s...
Amyloid light chain (AL) amyloidosis and multiple myeloma (MM) are both clonal plasma cell disorders...
International audienceUNLABELLED: DEFINITION OF THE DISEASE: AL amyloidosis results from extra-cellu...
The diagnosis of primary systemic amyloidosis, also known as AL (amyloid light-chain) amyloidosis, i...
Amyloidosis is a rare disease that is often seen in conjunction with multiple myeloma (MM). Its dama...
报告1例原发性系统性淀粉样变性并发多发性骨髓瘤.患者男,68岁.表现为紫癜、瘀斑、斑块的原发性系统性淀粉样变性,患者曾被多次误诊,最终确诊为原发性系统性淀粉样变性并发多发性骨髓瘤.中文核心期刊要目总览...
Immunoglobulin light chain (AL) amyloidosis is a systemic disease in which different systems such as...
Multiple myeloma (MM) is an immunoglobulin-producing tumor of plasma cells, which occurs commonly in...
International audienceIntroductionAL amyloidosis is caused by the proliferation of an immunoglobulin...
Amyloidosis is a systemic illness characterized by the extracellular deposition of abnormal proteins...