Light- and Heavy-chain Deposition Disease (LHCDD): Difficulty in Diagnosis and Treatment-Reference-Cited by-同舟云学术

Light- and Heavy-chain Deposition Disease (LHCDD): Difficulty in Diagnosis and Treatment

Published:2005 Issue:9 Volume:44 Page:915-916
ISSN:0918-2918
Container-title:Internal Medicine
language:en
Short-container-title:Intern. Med.

Author:

SUZUKI Kenshi¹

Affiliation:

1. Department of Hematology, Japanese Red Cross Medical Center, Hiroo, Shibuya-ku, Tokyo

Publisher

Japanese Society of Internal Medicine

Subject

General Medicine,Internal Medicine

Link

http://www.jstage.jst.go.jp/article/internalmedicine/44/9/44_9_915/_pdf

Reference5 articles.

1. 1) Buxbaum J. Mechanisms of disease: monoclonal immunoglobulin deposition. Amyloidosis, light chain deposition disease, and light and heavy chain deposition disease. Hematol Oncol Clin North Am 6: 323-346, 1992.

2. 2) Gallo GR, Lazowski P, Kumar A, et al. Renal and cardiac manifestations of B-cell dyscrasias with nonamyloidotic monoclonal light chain and light and heavy chain deposition diseases. Adv Nephrol Necker Hosp 28: 355-382, 1998.

3. High dose Chemotherapy and Stem Cell Support in a Patient of Light- and Heavy-chain Deposition Disease with Abnormal Marrow Cell Surface Antigens and No Monoclonal protein

4. 4) Fermand JP, Ravaud P, Chevret S, et al. High-dose therapy and autologous peripheral blood stem cell transplantation in multiple myeloma: Up-front or rescue treatment? Results of a multicenter sequential randomized clinical trial. Blood 92: 3131-3136, 1998.

5. 5) Skinner M, Sanchorawala V, Seldin DC, et al. High-dose melphalan and autologous stem-cell transplantation in patients with AL amyloidosis: An 8-year study. Ann Intern Med 140: 85-93, 2004.

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