AL amyloidosis that presented with marked hepatomegaly and polyclonal hypergammaglobulinemia
Author:
Affiliation:
1. Department of Hematology, Tenri Hospital
2. Department of Gastroenterology, Tenri Hospital
3. Department of Diagnostic Pathology, Tenri Hospital
Publisher
Tenri Foundation, Tenri Institute of Medical Research
Link
https://www.jstage.jst.go.jp/article/tenrikiyo/20/1/20_20-008/_pdf
Reference27 articles.
1. 1. Kastritis E, Dimopoulos MA. Recent advances in the management of AL Amyloidosis. Br J Haematol 2016;172:170-186.
2. 2. Muchtar E, Buadi FK, Dispenzieri A, et al. Immunoglobulin light-chain amyloidosis: From basics to new developments in diagnosis, prognosis and therapy. Acta Haematol 2016;135:172-190.
3. 3. McKenna RW, Kyle RA, Kuehl WM, et al. Plasma cell neoplasms. In: Swerdlow SH, Campo E, Harris NL, et al., eds. World Health Organization Classification of Tumours of Haematopoietic and Lymphoid Tissues. Lyon: IARC; 2008:200-213.
4. 4. Kyle RA, Gertz MA. Primary systemic amyloidosis: Clinical and laboratory features in 474 cases. Semin Hematol 1995;32:45-59.
5. 5. Gertz MA, Comenzo R, Falk RH, et al. Definition of organ involvement and treatment response in immunoglobulin light chain amyloidosis (AL): A consensus opinion from the 10th International Symposium on Amyloid and Amyloidosis, Tours, France, 18-22 April 2004. Am J Hematol 2005;79:319-328.
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