| Literature DB >> 16625338 |
Yasuhiro Horiuchi1, Junichi Hakugawa, Kazuhiro Shimizu, Ichiro Katayama, Tomayoshi Hayashi, Masahiro Kikuchi.
Abstract
The Sjögren syndrome often gives rise to complications such as pseudolymphomas and/or mucosa-/skin-associated lymphocytic tumors (MALT/SALT lymphomas). This paper presents a 74-year-old female patient with the Sjögren syndrome complicated by cutaneous plaques/tumors as cutaneous lymphoid hyperplasia over a 7-year follow-up study period. Immunohistochemical examination disclosed B-cell rich lymphoid follicle formation in the skin with the presence of T and B cells and a varied assortment of features to include abundant plasma cell infiltration. Based on the clinical course and histopathological findings, patient condition was considered benign and arises from reaction toward certain unknown microbes.Entities:
Mesh:
Year: 2006 PMID: 16625338 DOI: 10.1007/s00296-006-0130-7
Source DB: PubMed Journal: Rheumatol Int ISSN: 0172-8172 Impact factor: 2.631