IgM monoclonal gammopathy with heavy-and-light-chain amyloidosis resembling fibrillary glomerulonephritis determined by tandem mass spectrometry: a case report

被引:6
作者
Adachi, Misa [1 ]
Kitamura, Mineaki [1 ,2 ]
Muta, Kumiko [1 ]
Maekawa, Akihiro [3 ]
Uramatsu, Tadashi [1 ]
Tadokoro, Masato [4 ]
Funakoshi, Satoshi [2 ]
Hisano, Satoshi [5 ]
Kuwahara, Naomi [6 ]
Shimizu, Akira [6 ]
Mukae, Hiroshi [7 ]
Nishino, Tomoya [1 ]
机构
[1] Nagasaki Univ, Dept Nephrol, Grad Sch Biomed Sci, Nagasaki, Japan
[2] Nagasaki Renal Ctr, Dept Nephrol, Nagasaki, Japan
[3] Nagasaki Med Ctr, Dept Nephrol, Omura, Japan
[4] Koritsu Shin Obama Hosp, Dept Nephrol, Nagasaki, Japan
[5] Univ Occupat & Environm Hlth, Sch Med, Dept Pathol, Kitakyushu, Fukuoka, Japan
[6] Nippon Med Sch, Dept Analyt Human Pathol, Tokyo, Japan
[7] Nagasaki Univ, Grad Sch Biomed Sci, Dept Resp Med, Nagasaki, Japan
关键词
Fibrillary glomerulonephritis; IgM gammopathy; Immunoglobulin heavy-and-light-chain amyloidosis; Laser micro dissection; Mass spectrometry; LASER MICRODISSECTION; DIAGNOSIS;
D O I
10.1186/s12882-020-01851-4
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background Fibrillary glomerulonephritis (FGN) is distinguished from amyloidosis by thicker fibrils and the lack of staining with histochemical dyes typically reactive with amyloid. However, congophilic FGN has been proposed recently and adding laser microdissection followed by mass spectrometry (LMD/MS) to conventional pathological methods would be helpful to diagnose FGN. Here, we report a patient initially diagnosed with FGN whose final pathological diagnosis was changed to immunoglobulin heavy-and-light-chain amyloidosis (AHL) after LMD/MS. Case presentation A 75-year-old male developed nephrotic syndrome. Protein electrophoresis showed IgM kappa type M proteinemia and he was diagnosed with IgM monoclonal gammopathy. A renal biopsy was performed and pathological examination showed marked periodic acid-Schiff-positive enlargement of the mesangial region and silver stain positivity, but weak direct fast scarlet staining. Immunofluorescence analysis showed monoclonal deposition of IgM-kappa chain in the glomerulus. Under electron microscopy, the fibrils were about 20 nm in diameter, which was thicker than typical amyloid fibrils. Based on these findings, the patient was diagnosed with FGN. Although cyclophosphamide and prednisolone were administered, his renal function deteriorated and progressed to end stage renal disease requiring maintenance hemodialysis. As congophilic FGN has been recognized since 2018, Congo red staining and LMD/MS were performed. The Congo red staining was positive and LMD/MS results indicated that this was a case of AHL. Conclusions We reported a case of mu and kappa chain AHL resembling FGN requiring LMD/MS for definitive diagnosis. Since FGN and amyloidosis exhibit pathological findings, even if Congo red staining is positive, LMD/MS needs to be considered in cases atypical pathological findings, such as silver stain positivity or thicker fibrils.
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页数:7
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