A Case of Cutaneous and Systemic Plasmacytosis with an Unusual Clinical Presentation.
- Author:
Deok Woo LEE
1
;
Ji Hye YANG
;
Chong Hyun WON
;
Sung Eun CHANG
;
Mi Woo LEE
;
Jee Ho CHOI
;
Kee Chan MOON
Author Information
1. Department of Dermatology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea. miumiu@amc.seoul.kr
- Publication Type:Case Report
- Keywords:
Cutaneous and systemic plasmacytosis;
Cutaneous plasmacytosis
- MeSH:
Humans;
Hypergammaglobulinemia;
Korea;
Neck;
Plasma Cells;
Skin Manifestations
- From:Korean Journal of Dermatology
2009;47(5):558-561
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Cutaneous and systemic plasmacytosis is a rare disorder that's characterized by a cutaneous plasma cell infiltrate accompanied by polyclonal hypergammaglobulinemia. Clinically, it appears as multiple red-brown plaques that mainly occur on the trunk, and this is sometimes associated with variable extracutaneous involvement. All the cases of cutaneous and systemic plasmacytosis reported in Korea have shown the typical skin manifestations on the trunk of the patients. Herein, we report on a case of cutaneous and systemic plasmacytosis and the patient presented with multiple erythematous to brownish patches on the face, neck and both axillary areas.
