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A Case of Intravascular Large B-cell Lymphoma Mimicking Systemic Lupus Erythematosus / 대한내과학회지
Korean Journal of Medicine ; : 746-751, 2015.
Article in Korean | WPRIM | ID: wpr-46988
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.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Arthritis / Psychotic Disorders / Seizures / Serositis / Autoimmune Diseases / Thrombocytopenia / Lymphoma, Non-Hodgkin / B-Lymphocytes / Lymphoma, B-Cell / Early Diagnosis Type of study: Diagnostic study / Screening study Language: Korean Journal: Korean Journal of Medicine Year: 2015 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Arthritis / Psychotic Disorders / Seizures / Serositis / Autoimmune Diseases / Thrombocytopenia / Lymphoma, Non-Hodgkin / B-Lymphocytes / Lymphoma, B-Cell / Early Diagnosis Type of study: Diagnostic study / Screening study Language: Korean Journal: Korean Journal of Medicine Year: 2015 Type: Article