Cargando…
IgM monoclonal gammopathy with heavy-and-light-chain amyloidosis resembling fibrillary glomerulonephritis determined by tandem mass spectrometry: a case report
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 (L...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7245905/ https://www.ncbi.nlm.nih.gov/pubmed/32448180 http://dx.doi.org/10.1186/s12882-020-01851-4 |
_version_ | 1783537843154452480 |
---|---|
author | Adachi, Misa Kitamura, Mineaki Muta, Kumiko Maekawa, Akihiro Uramatsu, Tadashi Tadokoro, Masato Funakoshi, Satoshi Hisano, Satoshi Kuwahara, Naomi Shimizu, Akira Mukae, Hiroshi Nishino, Tomoya |
author_facet | Adachi, Misa Kitamura, Mineaki Muta, Kumiko Maekawa, Akihiro Uramatsu, Tadashi Tadokoro, Masato Funakoshi, Satoshi Hisano, Satoshi Kuwahara, Naomi Shimizu, Akira Mukae, Hiroshi Nishino, Tomoya |
author_sort | Adachi, Misa |
collection | PubMed |
description | 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 κ 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-κ 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 μ and κ 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. |
format | Online Article Text |
id | pubmed-7245905 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-72459052020-06-01 IgM monoclonal gammopathy with heavy-and-light-chain amyloidosis resembling fibrillary glomerulonephritis determined by tandem mass spectrometry: a case report Adachi, Misa Kitamura, Mineaki Muta, Kumiko Maekawa, Akihiro Uramatsu, Tadashi Tadokoro, Masato Funakoshi, Satoshi Hisano, Satoshi Kuwahara, Naomi Shimizu, Akira Mukae, Hiroshi Nishino, Tomoya BMC Nephrol Case Report 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 κ 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-κ 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 μ and κ 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. BioMed Central 2020-05-24 /pmc/articles/PMC7245905/ /pubmed/32448180 http://dx.doi.org/10.1186/s12882-020-01851-4 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Adachi, Misa Kitamura, Mineaki Muta, Kumiko Maekawa, Akihiro Uramatsu, Tadashi Tadokoro, Masato Funakoshi, Satoshi Hisano, Satoshi Kuwahara, Naomi Shimizu, Akira Mukae, Hiroshi Nishino, Tomoya IgM monoclonal gammopathy with heavy-and-light-chain amyloidosis resembling fibrillary glomerulonephritis determined by tandem mass spectrometry: a case report |
title | IgM monoclonal gammopathy with heavy-and-light-chain amyloidosis resembling fibrillary glomerulonephritis determined by tandem mass spectrometry: a case report |
title_full | IgM monoclonal gammopathy with heavy-and-light-chain amyloidosis resembling fibrillary glomerulonephritis determined by tandem mass spectrometry: a case report |
title_fullStr | IgM monoclonal gammopathy with heavy-and-light-chain amyloidosis resembling fibrillary glomerulonephritis determined by tandem mass spectrometry: a case report |
title_full_unstemmed | IgM monoclonal gammopathy with heavy-and-light-chain amyloidosis resembling fibrillary glomerulonephritis determined by tandem mass spectrometry: a case report |
title_short | IgM monoclonal gammopathy with heavy-and-light-chain amyloidosis resembling fibrillary glomerulonephritis determined by tandem mass spectrometry: a case report |
title_sort | igm monoclonal gammopathy with heavy-and-light-chain amyloidosis resembling fibrillary glomerulonephritis determined by tandem mass spectrometry: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7245905/ https://www.ncbi.nlm.nih.gov/pubmed/32448180 http://dx.doi.org/10.1186/s12882-020-01851-4 |
work_keys_str_mv | AT adachimisa igmmonoclonalgammopathywithheavyandlightchainamyloidosisresemblingfibrillaryglomerulonephritisdeterminedbytandemmassspectrometryacasereport AT kitamuramineaki igmmonoclonalgammopathywithheavyandlightchainamyloidosisresemblingfibrillaryglomerulonephritisdeterminedbytandemmassspectrometryacasereport AT mutakumiko igmmonoclonalgammopathywithheavyandlightchainamyloidosisresemblingfibrillaryglomerulonephritisdeterminedbytandemmassspectrometryacasereport AT maekawaakihiro igmmonoclonalgammopathywithheavyandlightchainamyloidosisresemblingfibrillaryglomerulonephritisdeterminedbytandemmassspectrometryacasereport AT uramatsutadashi igmmonoclonalgammopathywithheavyandlightchainamyloidosisresemblingfibrillaryglomerulonephritisdeterminedbytandemmassspectrometryacasereport AT tadokoromasato igmmonoclonalgammopathywithheavyandlightchainamyloidosisresemblingfibrillaryglomerulonephritisdeterminedbytandemmassspectrometryacasereport AT funakoshisatoshi igmmonoclonalgammopathywithheavyandlightchainamyloidosisresemblingfibrillaryglomerulonephritisdeterminedbytandemmassspectrometryacasereport AT hisanosatoshi igmmonoclonalgammopathywithheavyandlightchainamyloidosisresemblingfibrillaryglomerulonephritisdeterminedbytandemmassspectrometryacasereport AT kuwaharanaomi igmmonoclonalgammopathywithheavyandlightchainamyloidosisresemblingfibrillaryglomerulonephritisdeterminedbytandemmassspectrometryacasereport AT shimizuakira igmmonoclonalgammopathywithheavyandlightchainamyloidosisresemblingfibrillaryglomerulonephritisdeterminedbytandemmassspectrometryacasereport AT mukaehiroshi igmmonoclonalgammopathywithheavyandlightchainamyloidosisresemblingfibrillaryglomerulonephritisdeterminedbytandemmassspectrometryacasereport AT nishinotomoya igmmonoclonalgammopathywithheavyandlightchainamyloidosisresemblingfibrillaryglomerulonephritisdeterminedbytandemmassspectrometryacasereport |