A Case of Intravascular Large B-cell Lymphoma Mimicking Systemic Lupus Erythematosus.
10.3904/kjm.2015.89.6.746
- Author:
Chan Keol PARK
1
;
Jeong Chan LEE
;
Seong Wook KANG
;
Seung Cheol SHIM
;
Hwan Jung YUN
;
Jin Man KIM
;
In Seol YOO
Author Information
1. Department of Internal Medicine, Chungnam National University Hospital, Daejeon, Korea.
- Publication Type:Case Report
- Keywords:
Lymphoma;
Lupus erythematosus, Systemic
- MeSH:
Anemia;
Arthritis;
Autoimmune Diseases;
B-Lymphocytes*;
Diagnosis;
Early Diagnosis;
Exanthema;
Fever;
Lupus Erythematosus, Systemic*;
Lymphoma;
Lymphoma, B-Cell*;
Lymphoma, Non-Hodgkin;
Nephritis;
Psychotic Disorders;
Seizures;
Serositis;
Thrombocytopenia
- From:Korean Journal of Medicine
2015;89(6):746-751
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Intravascular large B-cell lymphoma (IVLBCL) is a rare subtype of non-Hodgkin's lymphoma (NHL) and that progresses rapidly and is usually fatal. Because it usually presents with nonspecific symptoms, such as fever, the early diagnosis of IVLBCL is very difficult and it is often misdiagnosed as another disease. Systemic lupus erythematosus (SLE) is an autoimmune disease that affects various organs. The clinical manifestation of SLE ranges from rash and arthritis through anemia and thrombocytopenia to serositis, nephritis, seizures, and psychosis. Thus, it can be easily confused with many other disorders. We report a case of IVLBCL mimicking SLE in the initial diagnosis.
