Podocyte Infolding Glomerulopathy (PIG) in a Patient With Undifferentiated Connective Tissue Disease: A Case Report.

Podocyte infolding glomerulopathy (PIG) is a recently described pathologic entity characterized by diffuse podocyte infolding into the glomerular basement membrane (GBM) associated with ultrastructurally demonstrable microspherular aggregates. The clinical features, significance, and pathogenesis of this condition are still not well delineated because only a few cases have been documented to date, all from Japan. We report a case of PIG associated with undifferentiated connective tissue disease in an Indian woman who presented with nephrotic syndrome while undergoing treatment for an autoimmune disorder. Ultrastructural analysis of the kidney biopsy specimen revealed unusual subepithelial aggregates of microspherules admixed with few microtubules alongside extensive infolding of podocyte foot processes into the underlying GBMs. Characteristic clustering of these microparticles near the invaginated tips of podocyte foot processes in the GBM was observed on transmission electron microscopy. The patient's clinical condition responded favorably to immunosuppressive therapy. The clinical, light microscopic, and diagnostic electron microscopic features of this condition are highlighted in this report in an attempt to contribute some insights into the possible pathogenetic mechanisms of this obscure entity.

[1]  H. Shigematsu,et al.  A case of podocytic infolding glomerulopathy with multiple myeloma , 2014, BMC Nephrology.

[2]  H. Makino,et al.  Proposal of podocytic infolding glomerulopathy as a new disease entity , 2008, Clinical and Experimental Nephrology.

[3]  Y. Fukuda,et al.  Invagination and infolding of podocytes in glomerular basement membrane in the cases of primary membranous nephropathy , 2008, Clinical and Experimental Nephrology.

[4]  H. Kitamura,et al.  A case report of glomerulopathy-associated podocytic infolding in a patient with tumor lysis syndrome , 2008, Clinical and Experimental Nephrology.

[5]  Y. Fukuda,et al.  A case of lupus nephritis with diffuse podocytic infolding into the glomerular basement membrane , 2008, Clinical and Experimental Nephrology.

[6]  T. Akizawa,et al.  A case of lupus nephritis coexisting with podocytic infolding associated with Takayasu’s arteritis , 2008, Clinical and Experimental Nephrology.

[7]  Shinsuke Nomura,et al.  Unusual glomerulopathy with aggregated subepithelial microspheric particles resembling membranous nephropathy: a variant of glomerulopathy associated with podocytic infolding? , 2008, Clinical and Experimental Nephrology.

[8]  H. Sugiyama,et al.  Unique microstructures and podocytic infolding in glomerular basement membrane associated with collagen diseases: a report of three cases , 2008, Clinical and Experimental Nephrology.

[9]  R. Katafuchi,et al.  Analysis of intra-GBM microstructures in a SLE case with glomerulopathy associated with podocytic infolding , 2008, Clinical and Experimental Nephrology.

[10]  Kentaro Koike,et al.  A case of glomerulopathy showing podocytic infolding in association with Sjögren’s syndrome and primary biliary cirrhosis , 2008, Clinical and Experimental Nephrology.

[11]  C. Alpers,et al.  Membranous glomerulopathy with spherules: an uncommon variant with obscure pathogenesis. , 2006, American journal of kidney diseases : the official journal of the National Kidney Foundation.

[12]  J. Haymann,et al.  Antenatal membranous glomerulonephritis with vascular injury induced by anti-neutral endopeptidase antibodies: toward new concepts in the pathogenesis of glomerular diseases. , 2003, Journal of the American Society of Nephrology : JASN.

[13]  J. Haymann,et al.  Antenatal membranous glomerulonephritis due to anti-neutral endopeptidase antibodies. , 2002, The New England journal of medicine.