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Primary systemic amyloidosis, acquired cutis laxa and cutaneous mucinosis in a patient with multiple myeloma / Amiloidose sistemica primaria, cutis laxa adquirida e mucinose cutanea em paciente com mieloma multiplo
Lavorato, Fernanda Guedes; Alves, Maria de Fatima Guimaraes Scotelaro; Maceira, Juan Manuel Pineiro; Unterstell, Natasha; Serpa, Laura Araujo; Azulay-Abulafia, Luna.
  • Lavorato, Fernanda Guedes; Rio de Janeiro State University. Pedro Ernesto University Hospital. Rio de Janeiro. BR
  • Alves, Maria de Fatima Guimaraes Scotelaro; Rio de Janeiro State University. Pedro Ernesto University Hospital. Rio de Janeiro. BR
  • Maceira, Juan Manuel Pineiro; Rio de Janeiro State University. Pedro Ernesto University Hospital. Rio de Janeiro. BR
  • Unterstell, Natasha; Rio de Janeiro State University. Pedro Ernesto University Hospital. Rio de Janeiro. BR
  • Serpa, Laura Araujo; Rio de Janeiro State University. Pedro Ernesto University Hospital. Rio de Janeiro. BR
  • Azulay-Abulafia, Luna; Rio de Janeiro State University. Pedro Ernesto University Hospital. Rio de Janeiro. BR
An. bras. dermatol ; 88(6,supl.1): 32-35, Nov-Dec/2013. tab, graf
Article in English | LILACS | ID: lil-696800
ABSTRACT
A 57-year-old woman presented with periorbital ecchymoses, laxity in skin folds, polyneuropathy and bilateral carpal tunnel syndrome. A skin biopsy of the axillary lesion demonstrated fragmentation of elastic fibers, but with a negative von Kossa stain, consistent with cutis laxa. The diagnosis of primary systemic amyloidosis was made by the presence of amyloid material in the eyelid using histopathological techniques, besides this, the patient was also diagnosed with purpura, polyneuropathy, bilateral carpal tunnel syndrome and monoclonal gammopathy. She was diagnosed as suffering from multiple myeloma based on the finding of 40% plasma cells in the bone marrow, component M in the urine and anemia. The patient developed blisters with a clear content, confirmed as mucinosis by the histopathological exam. The final diagnoses were primary systemic amyloidosis, acquired cutis laxa and mucinosis, all related to multiple myeloma.
RESUMO
Mulher de 57 anos, com equimose periorbitária, frouxidão cutânea nas dobras, polineuropatia e síndrome do túnel do carpo bilateral.O exame histopatológico da lesão axilar revelou fragmentação de fibras elásticas, porém a coloração de von Kossa foi negativa;o diagnóstico foi de cútis laxa. Amiloidose sistêmica primária foi confirmada pela presença de material amilóide no exame histopatológico da pálpebra, além de púrpura, polineuropatia, síndrome do túnel do carpo bilateral e gamopatia monoclonal. Foi diagnosticada como portadora de mieloma múltiplo por apresentar 40% de plasmócitos na medula óssea, componente M urinário e anemia. A paciente evoluiu com bolhas de conteúdo citrino, cujo exame histopatológico mostrou mucinose. Os diagnósticos finais foram amiloidose sistêmica primária, cútis laxa adquirida e mucinose, todos vinculados ao mieloma múltiplo.
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Full text: Available Index: LILACS (Americas) Main subject: Skin Diseases / Mucinoses / Cutis Laxa / Amyloidosis / Multiple Myeloma Limits: Female / Humans Language: English Journal: An. bras. dermatol Journal subject: Dermatology Year: 2013 Type: Article Affiliation country: Brazil Institution/Affiliation country: Rio de Janeiro State University/BR

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Full text: Available Index: LILACS (Americas) Main subject: Skin Diseases / Mucinoses / Cutis Laxa / Amyloidosis / Multiple Myeloma Limits: Female / Humans Language: English Journal: An. bras. dermatol Journal subject: Dermatology Year: 2013 Type: Article Affiliation country: Brazil Institution/Affiliation country: Rio de Janeiro State University/BR