Horiuchi Yasuhiro, Hakugawa Junichi, Shimizu Kazuhiro, Katayama Ichiro, Hayashi Tomayoshi, Kikuchi Masahiro
Department of Dermatology, Nagasaki University School of Medicine, 1-7-1 Sakamoto, 852-8501 Nagasaki, Japan.
Rheumatol Int. 2006 Sep;26(11):1044-9. doi: 10.1007/s00296-006-0130-7. Epub 2006 Apr 20.
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.