Cutaneous light chain amyloidosis with multiple myeloma: A concise review

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Immunoglobulin light chain amyloidosis associated with multiple myeloma in a young patient: a case report.

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.

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Tetany and osteolysis in light chain myeloma with amyloidosis.

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Case for diagnosis. Systemic light chain amyloidosis with cutaneous involvement*

Systemic light chain amiloydosis is a rare disease. Due to its typical cutaneous lesions, dermatologists play an essential role in its diagnosis. Clinical manifestations vary according to the affected organ and are often unspecific. Definitive diagnosis is achieved through biopsy. We report a patient with palpebral amyloidosis, typical bilateral ecchymoses and cardiac involvement, without plasm...

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The occurrence of Al amyloidosis (light-chain amyloidosis) in patients with multiple myeloma in Lower Silesia Region, Poland.

BACKGROUND The incidence of amyloidosis is difficult to determine because the disease is often undiagnosed or diagnosed incorrectly. In Polish studies, there are no statistics and analyses of the factors that may influence the development of amyloidosis in patients with multiple myeloma. OBJECTIVES The goal of this study was to estimate the incidence of AL amyloidosis in MM patients in Lower ...

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ژورنال

عنوان ژورنال: Hematology/Oncology and Stem Cell Therapy

سال: 2019

ISSN: 1658-3876

DOI: 10.1016/j.hemonc.2018.09.003