Literature DB >> 8172222

The fibrillary glomerulopathies.

S M Korbet1, M M Schwartz, E J Lewis.   

Abstract

Fibrillary glomerulopathy is a category of glomerular disease that is defined by the ultrastructural feature of organized deposits of extracellular, nonbranching, microfibrils. The best-known disease in this category is amyloidosis, but cryoglobulinemia, light chain deposition disease, systemic lupus erythematosus, immunotactoid glomerulopathy, and diabetic fibrillosis may have similar ultrastructural findings and comprise the differential diagnosis of the fibrillary glomerulopathies. Because they have disease-specific therapeutic and prognostic implications, differentiating among these entities is important for nephrologists and nephropathologists. To aid the physician, we will review the fibrillary glomerulopathies using an algorithm based on morphology, clinical features, and serologic assessment. We believe this approach will prove to be practical and useful to the practicing nephrologist.

Entities:  

Mesh:

Year:  1994        PMID: 8172222     DOI: 10.1016/s0272-6386(12)70290-1

Source DB:  PubMed          Journal:  Am J Kidney Dis        ISSN: 0272-6386            Impact factor:   8.860


  11 in total

1.  Glomerular mesangial fibrillary deposits in a patient with diabetes mellitus.

Authors:  Ipek Isik Gonul; James Gough; Kim Jim; Hallgrimur Benediktsson
Journal:  Int Urol Nephrol       Date:  2007-01-09       Impact factor: 2.370

2.  Rare diagnosis in a patient with diabetes with nephrotic proteinuria.

Authors:  Ariana Azevedo; Patrícia Cotovio; Mário Góis; Fernando Nolasco
Journal:  BMJ Case Rep       Date:  2019-01-10

3.  Clinical Features and Outcomes of a Racially Diverse Population with Fibrillary Glomerulonephritis.

Authors:  Fernanda Payan Schober; Meghan A Jobson; Caroline J Poulton; Harsharan K Singh; Volker Nickeleit; Ronald J Falk; J Charles Jennette; Patrick H Nachman; William F Pendergraft Iii
Journal:  Am J Nephrol       Date:  2017-02-04       Impact factor: 3.754

4.  [Lupus nephritis with crystal structures in glomerulopathy ].

Authors:  M Otto; T Hansen; S Bertz; E H Strøm; S H Brorson; M J Mihatsch; J Kriegsmann
Journal:  Pathologe       Date:  2003-10       Impact factor: 1.011

5.  A case of immunotactoid glomerulopathy exhibiting nephrotic syndrome successfully treated with corticosteroids and antihypertensive therapy.

Authors:  Masaru Kinomura; Yohei Maeshima; Ryo Kodera; Hiroshi Morinaga; Daisuke Saito; Kazushi Nakao; Hiroyuki Yanai; Kenei Sada; Hitoshi Sugiyama; Hirofumi Makino
Journal:  Clin Exp Nephrol       Date:  2009-04-15       Impact factor: 2.801

Review 6.  Amyloid in surgical pathology.

Authors:  Christoph Röcken; Knut Sletten
Journal:  Virchows Arch       Date:  2003-06-11       Impact factor: 4.064

7.  Fibrillary glomerulonephritis and renal failure in a child with systemic lupus erythematosus.

Authors:  Shina Menon; Xu Zeng; Rudolph Valentini
Journal:  Pediatr Nephrol       Date:  2009-03-24       Impact factor: 3.714

8.  When the finding of glomerular fibrils in patients with nephrotic syndrome leads to an erroneous diagnosis.

Authors:  Ana Huerta; Beatriz Segovia; Aurelio Hernández; Enrique Morales; Jorge González; Eva Mérida; Miguel Angel Martínez; Manuel Praga
Journal:  NDT Plus       Date:  2008-11-12

9.  Ultrastructural pathology of nephropathies with organized deposits: a case series.

Authors:  Fabio Fabbian; Nevio Stabellini; Adriana Galdi; Sergio Sartori; Arrigo Aleotti; Luigi Catizone
Journal:  Cases J       Date:  2008-09-25

10.  Familial Mediterranean fever, inflammation and nephrotic syndrome: fibrillary glomerulopathy and the M680I missense mutation.

Authors:  Patrick W Fisher; L Tammy Ho; Robert Goldschmidt; Ronald J Semerdjian; Gregory W Rutecki
Journal:  BMC Nephrol       Date:  2003-08-11       Impact factor: 2.388

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