Primary cutaneous amyloidosis (PCA) is a chronic pruritic skin disorder of unknown origin. We report on the case of a 48-year-old Indian woman with diffuse biphasic amyloidosis in which UVA1 phototherapy resulted in marked improvement of skin lesions and pruritus. UVA1 phototherapy was administered as monotherapy five times a week for 3 weeks with an exposure at a single dose of 130 J/cm2 resulting in a cumulative UVA1 dose of 1950 J/cm2. After treatment, the skin appeared less pigmented with flattened papules, and the histology revealed the disappearance of amyloid deposits and the presence of melanophages in the dermis. A comprehensive review of the literature on the treatment options for PCA showed no controlled trials available. However, case series indicated phototherapy (UVB, narrow band UVB, photochemotherapy) as the most successful treatment

Ultraviolet-A1 phototherapy in the treatment of primary diffuse cutaneous amyloidosis: an additional phototherapy regimen for cutaneous amyloidosis with review of treatment options

GISONDI, Paolo;GIROLOMONI, Giampiero
2015-01-01

Abstract

Primary cutaneous amyloidosis (PCA) is a chronic pruritic skin disorder of unknown origin. We report on the case of a 48-year-old Indian woman with diffuse biphasic amyloidosis in which UVA1 phototherapy resulted in marked improvement of skin lesions and pruritus. UVA1 phototherapy was administered as monotherapy five times a week for 3 weeks with an exposure at a single dose of 130 J/cm2 resulting in a cumulative UVA1 dose of 1950 J/cm2. After treatment, the skin appeared less pigmented with flattened papules, and the histology revealed the disappearance of amyloid deposits and the presence of melanophages in the dermis. A comprehensive review of the literature on the treatment options for PCA showed no controlled trials available. However, case series indicated phototherapy (UVB, narrow band UVB, photochemotherapy) as the most successful treatment
2015
primary cutaneous amyloidosis; biphasic amyloidosis; ultraviolet A1 phototherapy
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11562/934699
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