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

Overview of attention for article published in Anais Brasileiros de Dermatologia, January 2017
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Title
Case for diagnosis. Systemic light chain amyloidosis with cutaneous involvement*
Published in
Anais Brasileiros de Dermatologia, January 2017
DOI 10.1590/abd1806-4841.20176958
Pubmed ID
Authors

João Renato Vianna Gontijo, Jackson Machado Pinto, Maysa Carla de Paula

Abstract

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 plasma cell dyscrasia or lymphomas. The patient died shortly after the diagnosis.

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Mendeley readers

The data shown below were compiled from readership statistics for 9 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 9 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 2 22%
Student > Bachelor 2 22%
Student > Doctoral Student 1 11%
Professor 1 11%
Student > Postgraduate 1 11%
Other 0 0%
Unknown 2 22%
Readers by discipline Count As %
Medicine and Dentistry 4 44%
Psychology 1 11%
Materials Science 1 11%
Social Sciences 1 11%
Unknown 2 22%