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 Printable version |
Extensive haemorrhagic-bullous skin manifestation of systemic AA-amyloidosis associated with Iglmyeloma |
European Journal of Dermatology. Volume 10, Number 2, 139-42, March 2000, Cas cliniques
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 Free Article
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Author(s) : J.-U. Grundmann, B. Bonnekoh, H. Gollnick |
Summary : In an 86-year-old woman with a multiple myeloma of the IgG lambda subtype a coinciding systemic amyloidosis manifested as a macroglossia, diffuse alopecia and generalized cutaneous involvement. The skin was affected by milium-like papules, petechial haemorrhages and an increased tissue fragility with subsequent blister formation. The typical histology and immunohistology pattern revealed large intradermal amyloid masses, reacting positively with anti-amyloid A antibodies, which surrounded cuff-like dilatated blood capillaries. The abundance of these amyloid deposits led to significant deflexibilization and fragility of the capillaries and the dermal matrix eventually resulting in the haemorrhagic-bullous eruptions. The peculiar feature of the present case is the extensity of bullous-haemorrhagic skin damage due to amyloid A deposition without any detection of cutaneous IgGl as the myeloma-derived paraprotein assumed to be causative for the development of systemic AA amyloidosis. |
Keywords : amyloid, protein storage disease, plasma cell dyscrasia. |
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