Skip to main content
Top
Published in: BMC Nephrology 1/2019

Open Access 01-12-2019 | Acute Kidney Injury | Case report

Case report: a peculiar glomerulopathy in a patient suffering from nephrotic syndrome

Authors: Fabian Wöstmann, Roman-Ulrich Müller, Heike Göbel, Thomas Benzing, Jan U. Becker, Malte P. Bartram

Published in: BMC Nephrology | Issue 1/2019

Login to get access

Abstract

Background

Podocyte infolding glomerulopathy (PIG) is a rare histopathologic finding with global infolding of the podocytes into the glomerular basement membrane (GBM), accompanied by microstructures underneath. Described in 2002 for the first time, PIG was proposed as a new pathological entity in 2008 based on the largest case series so far. Yet all of the described cases derive from Asian countries. We report a case from Germany fulfilling the diagnostic criteria of PIG. Considering the scarcity of data on this entity especially in Western countries, collecting cases like ours and multicentric meta-analyses will be crucial to obtain a better understanding of PIG, its causes, clinical course and potential treatment options.

Case presentation

A 56-year-old Caucasian woman with a history of rheumatoid arthritis (RA), no other comorbidities and no known renal disease was admitted to the hospital with acute kidney injury (AKI) and nephrotic syndrome. Physical examination was unremarkable except for anasarca. Renal ultrasound revealed no abnormalities. Laboratory and urine analyses were consistent with the nephrotic syndrome and renal failure. Serological studies regarding ANA, ANCA, anti-PLA2R autoantibodies, complement, virus infections, immunofixation and quantitative light chain analysis were unremarkable. A renal biopsy was performed. Light microscopic examination showed flattened tubular epithelium consistent with acute tubular damage, no infiltrates and unremarkable glomeruli except diffuse and global holes in the GBM (Fig. 1a) and negative staining for immunoglobulin heavy-chains, light-chains and complement split products. Electron microscopy revealed a rare correlate for these holes: global peculiar infolding of podocyte cytoplasm into the GBM. Most of these infoldings were accompanied by condensation of the GBM underneath. No such condensation or electron dense deposits were found without these infoldings or outside the GBM.

Conclusion

Here we report the first case of PIG outside of Asia. Since there are only few reports about this specific finding, we feel there is a need to share information in an attempt to accumulate knowledge about this possible new entity and potential treatment options.
Literature
1.
go back to reference Joh K, Taguchi T, Shigematsu H, Kobayashi Y, Sato H, Nishi S, Katafuchi R, Nomura S, Fujigaki Y, Utsunomiya Y, Sugiyama H, Saito T, Makino H. Proposal of podocytic infolding glomerulopathy as a new disease entity. A review of 25 cases from nationwide research in Japan. Clin Exp Nephrol. 2008;12:421–31.CrossRef Joh K, Taguchi T, Shigematsu H, Kobayashi Y, Sato H, Nishi S, Katafuchi R, Nomura S, Fujigaki Y, Utsunomiya Y, Sugiyama H, Saito T, Makino H. Proposal of podocytic infolding glomerulopathy as a new disease entity. A review of 25 cases from nationwide research in Japan. Clin Exp Nephrol. 2008;12:421–31.CrossRef
2.
go back to reference Kwon KW, Jeong HJ, Lee JH. Podocytic infolding glomerulopathy. A case report. Ultrastruct Pathol. 2016;40:374–7.CrossRef Kwon KW, Jeong HJ, Lee JH. Podocytic infolding glomerulopathy. A case report. Ultrastruct Pathol. 2016;40:374–7.CrossRef
3.
go back to reference Matthai SM, Mohapatra A, Mathew AJ, Roy S, Varughese S, Danda D, Tamilarasi V. Podocyte Infolding Glomerulopathy (PIG) in a patient with undifferentiated connective tissue disease. Am J Kidney Dis. 2018;72(1):149–53.CrossRef Matthai SM, Mohapatra A, Mathew AJ, Roy S, Varughese S, Danda D, Tamilarasi V. Podocyte Infolding Glomerulopathy (PIG) in a patient with undifferentiated connective tissue disease. Am J Kidney Dis. 2018;72(1):149–53.CrossRef
4.
go back to reference Harada M, Kamijo Y, Ehara T, Shimojo H, Shigematsu H, Higuchi M. A case of podocytic infolding glomerulopathy with multiple myeloma. BMC Nephrol. 2014;15:32.CrossRef Harada M, Kamijo Y, Ehara T, Shimojo H, Shigematsu H, Higuchi M. A case of podocytic infolding glomerulopathy with multiple myeloma. BMC Nephrol. 2014;15:32.CrossRef
5.
go back to reference Fujigaki Y, Muranaka Y, Sakakima M, Ohta I, Sakao Y, Fujikura T, Sun Y, Katafuchi R, Joh K, Hishida A. Analysis of intra-GBM microstructures in a SLE case with glomerulopathy associated with podocytic infolding. Clin Exp Nephrol. 2008;12:432–9.CrossRef Fujigaki Y, Muranaka Y, Sakakima M, Ohta I, Sakao Y, Fujikura T, Sun Y, Katafuchi R, Joh K, Hishida A. Analysis of intra-GBM microstructures in a SLE case with glomerulopathy associated with podocytic infolding. Clin Exp Nephrol. 2008;12:432–9.CrossRef
6.
go back to reference Masuda Y, Mii A, Shimizu A, Fujita E, Aki K, Ishikawa K, Ishizaki M, Sato S, Hayama N, Iino Y, Katayama Y, Fukuda Y. Invagination and infolding of podocytes in glomerular basement membrane in the cases of primary membranous nephropathy. Clin Exp Nephrol. 2008;12:440–9.CrossRef Masuda Y, Mii A, Shimizu A, Fujita E, Aki K, Ishikawa K, Ishizaki M, Sato S, Hayama N, Iino Y, Katayama Y, Fukuda Y. Invagination and infolding of podocytes in glomerular basement membrane in the cases of primary membranous nephropathy. Clin Exp Nephrol. 2008;12:440–9.CrossRef
7.
go back to reference Matsuo T, Kobayashi Y, Nemoto N, Sano T, Kamata K, Shigematsu H. A nephrotic case of vesicoureteral reflux representing focal segmental glomerulosclerosis associated with podocytic infolding lesions. Clin Exp Nephrol. 2008;12:494–500.CrossRef Matsuo T, Kobayashi Y, Nemoto N, Sano T, Kamata K, Shigematsu H. A nephrotic case of vesicoureteral reflux representing focal segmental glomerulosclerosis associated with podocytic infolding lesions. Clin Exp Nephrol. 2008;12:494–500.CrossRef
8.
go back to reference Iguchi A, Sohma A, Yamazaki H, Ito T, Saeki T, Ito Y, Imai N, Osawa Y, Narita I. A case of podocytic infolding glomerulopathy with focal segmental glomerulosclerosis. Case reports in nephrology and urology. 2013;3:110–6.CrossRef Iguchi A, Sohma A, Yamazaki H, Ito T, Saeki T, Ito Y, Imai N, Osawa Y, Narita I. A case of podocytic infolding glomerulopathy with focal segmental glomerulosclerosis. Case reports in nephrology and urology. 2013;3:110–6.CrossRef
Metadata
Title
Case report: a peculiar glomerulopathy in a patient suffering from nephrotic syndrome
Authors
Fabian Wöstmann
Roman-Ulrich Müller
Heike Göbel
Thomas Benzing
Jan U. Becker
Malte P. Bartram
Publication date
01-12-2019
Publisher
BioMed Central
Published in
BMC Nephrology / Issue 1/2019
Electronic ISSN: 1471-2369
DOI
https://doi.org/10.1186/s12882-019-1478-8

Other articles of this Issue 1/2019

BMC Nephrology 1/2019 Go to the issue