Literature DB >> 22481660

Primary systemic amyloidosis associated with multiple myeloma.

Ederson Valei Lopes de Oliveira1, Ana Carolina Garcia Pozetti, Eurides Maria de Oliveira Pozetti, João Roberto Antonio, Nilceo Schwery Michalany.   

Abstract

This case report is about a 48-year-old female patient with systemic amyloidosis and multiple myeloma simultaneously. Amyloid cutaneous infiltrative lesions like papules, nodules, or plaques with a serous-hemorrhagic aspect were found in the eyelids, neck and retroauricular region, among others. She had presented intermittent papular lesions on the upper eyelids one year before, which worsened following local trauma. A local skin biopsy showed amorphous and eosinophilic substance in the dermis. Congo red staining confirmed the amyloid deposits. Abnormal exams: proteinuria (570 mg/24h), Bence-Jones proteinuria and clonal plasma cells (70%) found in myelogram. Following the diagnosis of multiple myeloma based on amyloid skin lesions, the patient was referred to the Hematology service and died 5 months after the diagnosis.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22481660     DOI: 10.1590/s0365-05962012000100015

Source DB:  PubMed          Journal:  An Bras Dermatol        ISSN: 0365-0596            Impact factor:   1.896


  1 in total

1.  Primary systemic amyloidosis, acquired cutis laxa and cutaneous mucinosis in a patient with multiple myeloma.

Authors:  Fernanda Guedes Lavorato; Maria de Fátima Guimarães Scotelaro Alves; Juan Manuel Piñeiro Maceira; Natasha Unterstell; Laura Araújo Serpa; Luna Azulay-Abulafia
Journal:  An Bras Dermatol       Date:  2013 Nov-Dec       Impact factor: 1.896

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.