Newly Developed Multiple Myeloma in a Patient with Primary T-Cell Lymphoma of Bone.
10.3346/jkms.2008.23.3.544
- Author:
Jun Eul HWANG
1
;
Sang Hee CHO
;
Ok Ki KIM
;
Hyun Jeong SHIM
;
Se Ryeon LEE
;
Jae Sook AHN
;
Duk Hwan YANG
;
Yeo Kyeoung KIM
;
Je Jung LEE
;
Hyeoung Joon KIM
;
Ik Joo CHUNG
Author Information
1. Department of Internal Medicine, Division of Hemato-Oncology, Chonnam National University Medical School, Gwangju, Korea. ijchung@chonnam.ac.kr
- Publication Type:Case Report
- Keywords:
Lymphoma, Non-Hodgkin;
Multiple Myeloma;
T-Cell Lymphoma of Bone
- MeSH:
Bone Neoplasms/*complications/diagnosis/therapy;
Fatal Outcome;
Humans;
Kidney Failure, Acute/etiology;
Lymphoma, T-Cell/*complications/diagnosis/therapy;
Male;
Middle Aged;
Multiple Myeloma/*complications/diagnosis/therapy
- From:Journal of Korean Medical Science
2008;23(3):544-547
- CountryRepublic of Korea
- Language:English
-
Abstract:
Primary non-Hodgkin's lymphoma of bone (PLB) is rare, and generally presents as a single extensive and destructive bone lesion. Histopathologically, most cases present as diffuse large B-cell lymphoma, and T-cell lymphoma is rare. By contrast, multiple myeloma is a disease defined as the neoplastic proliferation of a single clone of plasma cells producing a monoclonal immunoglobulin. We report a case of multiple myeloma that developed during treatment of PLB in a type of T-cell. A 48-yr-old man was diagnosed as T-cell PLB, stage IE, 18 months ago. The patient received the chemoradiotherapy and salvage chemotherapy for PLB. However, the lymphoma progressed with generalized bone pain, and laboratory findings showed bicytopenia and acute renal failure. On bone marrow biopsy, the patient was diagnosed as having multiple myeloma newly developed with primary T-cell lymphoma of bone. In spite of chemotherapy, the patient died of renal failure.