Herrero Laura, Naranjo-Hans Dolores, Solé Manel, Santamaría Gorane, Bargalló Xavier, Velasco Martín, Fernández Pedro Luis
Department of Pathology, Hospital Clinic, University of Barcelona, Barcelona, Spain.
Pathobiology. 2015;82(6):264-8. doi: 10.1159/000440866. Epub 2015 Oct 30.
Amyloidosis involving the breast is a rare finding and it may present as a solitary mass called 'amyloid tumor'. According to the largest case series, the amyloid deposits are usually of the AL type (commonly x03BA; light chain).
We report 3 cases diagnosed at our institution in the period from 2000 to 2015. Radiological, histological and immunohistochemical studies were performed.
Together with a case presenting in a patient with multiple myeloma, we describe 2 unique presentations including 1 associated with CREST syndrome in a patient with a previous history of breast carcinoma and another, also associated with cancer, with transthyretin deposits in a woman with a TTR gene mutation and a family history of familial amyloidotic polyneuropathy. These cases are an example of the vast heterogeneity of this disorder regarding its clinical presentation, the type of amyloid deposits and other diseases associated with breast amyloidosis.
