| Literature DB >> 18266125 |
J Pérez-Martínez, M Marques, L Kilmurray, I Medina, S H Nam-Cha, F Llamas, C Gómez, A Barrientos, J Blanco.
Abstract
We report a 34-year-old man diagnosed with Langerhans cell histiocytosis (LCH) or histiocytosis X in 1980. He had multiple focal osseous lesions, difficult control of the disease activity and was treated many times with chemo- and radiotherapy for symptomatic control. His kidney disease started 20 years after the diagnosis with progressive renal failure and increasing non-nephrotic proteinuria, coinciding with two flares of LCH. A percutaneous renal biopsy demonstrated amyloidosis. There is only one case described in the amyloidosis literature associated with LCH.Entities:
Mesh:
Year: 2008 PMID: 18266125 DOI: 10.1080/13506120701816827
Source DB: PubMed Journal: Amyloid ISSN: 1350-6129 Impact factor: 7.141