| Literature DB >> 28508971 |
Masaaki Yanishi1, Hiroyasu Tsukaguchi2, Takashi Yoshida3, Hisanori Taniguchi3, Kenji Yoshida3, Takao Mishima3, Yoshihiro Komai3, Kaneki Yasuda3, Masato Watanabe3, Motohiko Sugi3, Hidefumi Kinoshita3, Tadashi Matsuda3.
Abstract
Monoclonal gammopathy of undetermined significance (MGUS) is the common pre-malignant B cell disorders with a general prevalence of 3-5 % at age over 50. Because of the potential malignant transformation and immune insufficiency, pre-transplant MGUS recipient should be carefully followed after allograft transplantation. The post-transplant prognosis and quality of life (QOL) in patient with MGUS have not yet been fully determined. The aim of this study is to evaluate function and pathology of the renal allograft and self-assessment QOL changes during 2 years after transplantation in our case of MGUS-bearing recipient. We here studied the clinical course and QOL improvement before and 20 months after transplant in a 56-year-old woman, who had pre-existing MGUS and underwent living donor kidney transplantation. After the renal allograft transplant, the patients maintained normal GFR and had neither acute rejections nor histologic evidence of renal injuries related to the monoclonal gammopathy on the protocol biopsy of 1 year post-transplant. During further 20 months follow-up, the pre-transplant MGUS remained uneventful without any hematologic abnormalities and other medical complications, i.e., infection. Evaluation of QOL using a self-assessment questionnaire showed significant improvement for physical and mental items on both 6 and 18 months post-transplant. The renal transplant thus successfully provided a greater satisfaction for the recipient on both physical and mental health aspects. Our observations suggest that renal transplantation is beneficial even in those who had pre-existing MGUS if managed and followed carefully, which ultimately could significantly improve the patient QOL.Entities:
Keywords: Kidney transplantation; Monoclonal gammopathy; QOL
Year: 2016 PMID: 28508971 PMCID: PMC5413755 DOI: 10.1007/s13730-016-0218-1
Source DB: PubMed Journal: CEN Case Rep ISSN: 2192-4449