Literature DB >> 30941743

Mucocutaneous manifestations in systemic amyloidosis A retrospective analytical study in a tertiary care center.

Luis-Rodrigo Flores-Bozo1, Josune Echevarría-Keel1, Judith Domínguez-Cherit1, Lilly Esquivel-Pedraza1,2, Silvia Méndez-Flores1.   

Abstract

BACKGROUND: The mucocutaneous clinical profile of patients with amyloidosis in Latin America has been scarcely reported.
OBJECTIVE: To describe clinical characteristics of skin and mucosal manifestations in systemic amyloidosis in a tertiary care center in Mexico City.
METHODS: A cross sectional, retrospective analytical study was performed in patients with systemic amyloidosis over a 15-year period. Statistical analysis was done.
RESULTS: A total of 98 patients were included (53 [54%] men; overall median age = 49 years old). Acquired systemic immunoglobulin light chain amyloidosis (AL) was the most common (49%) type, followed by (24.5%) wild-type transthyretin amyloidosis (H-TTR) (24.5%), undetermined cases (21%), and reactive systemic amyloidosis (AA) (6.1%). There were mucocutaneous manifestations in 34.7% of cases, mostly multiple myeloma-related AL (ALMM). Head and neck was the most often affected site (38.2%), and purpuric macules were the most common morphology (44.1%). Mucocutaneous affectation was predominantly observed in AL (50.0%) compared to other types (20.0%) of amyloidosis (P = 0.01). Likewise, involvement of organs was also significantly different among the diverse amyloidosis types (P < 0.05). The most frequent comorbidities were hypertension (18.3%) and hypothyroidism (18.3%).
CONCLUSION: The clinical spectrum of manifestations in amyloidosis is wide. Involvement of skin and mucosa in amyloidosis is common; significant differences were observed concerning distribution of mucocutaneous amyloid manifestations among the different types of amyloidosis.
© 2019 The International Society of Dermatology.

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Year:  2019        PMID: 30941743     DOI: 10.1111/ijd.14443

Source DB:  PubMed          Journal:  Int J Dermatol        ISSN: 0011-9059            Impact factor:   2.736


  1 in total

1.  Autopsy findings in a patient with primary systemic AL (kappa light chain) amyloidosis.

Authors:  Felipe Lourenço Ledesma; Jussara Bianchi Castelli
Journal:  Autops Case Rep       Date:  2021-05-06
  1 in total

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