Related Experiment Video
Updated: Mar 18, 2026

Methods to Classify Cytoplasmic Foci as Mammalian Stress Granules
Published on: May 12, 2017
FSGS: from pathogenesis to the histological lesion
Andrea Angioi1, Antonello Pani2
1Division of Nephrology and Dialysis, Azienda Ospedaliera G.Brotzu, Cagliari, Italy.
Focal and segmental glomerulosclerosis (FSGS) presents diagnostic challenges, encompassing both a histological pattern and a specific kidney disease. Precise classification of FSGS lesions requires experienced renal teams due to complex etiological factors.
Area of Science:
- Nephrology
- Pathology
- Renal Medicine
Background:
- Focal and segmental glomerulosclerosis (FSGS) is a complex kidney disease.
- It can represent a histological pattern of injury or a distinct pauci-immune podocytopathy.
- Current understanding acknowledges diverse etiological classes contributing to FSGS lesions.
Purpose of the Study:
- To clarify the dual nature of FSGS terminology.
- To discuss the challenges in precise classification of FSGS lesions.
- To highlight the etiological diversity associated with FSGS.
Main Methods:
- Review of current and past literature on FSGS.
- Analysis of diagnostic criteria and clinical practice.
- Discussion of etiological factors including reactive, genetic, adaptive, proliferative, and inflammatory forms.
Main Results:
- FSGS can describe a morphological pattern or a specific podocytopathy.
- Practical tools for precise FSGS classification are limited.
- Diagnosis relies heavily on the expertise of nephrologists and pathologists.
Conclusions:
- Accurate diagnosis of FSGS requires a multidisciplinary approach.
- Further research may lead to improved classification tools.
- Clinical, serological, and histological expertise is crucial for managing FSGS.
More Related Videos
06:35An Immunohistopathologic Study to Profile the Folate Receptor Beta Macrophage and Vascular Immune Microenvironment in Giant Cell Arteritis
Published on: February 8, 2019
11:37Immunofluorescence Analysis of Stress Granule Formation After Bacterial Challenge of Mammalian Cells
Published on: July 3, 2017
Related Concept Videos
Cystic Fibrosis: Pathogenesis
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
Amyloid Fibrils
Amyloid deposits were observed as early as 1639 in the liver and the spleen. In 1854, Rudolph Virchow performed iodine staining,...
Gastritis-II: Pathophysiology
In acute gastritis, the gastric mucosa becomes swollen and red and undergoes superficial erosion. Superficial ulceration may lead to bleeding.
In chronic gastritis, persistent or repeated insults lead to chronic inflammatory changes and, eventually, thinning or atrophy of the gastric tissue.
Gastritis can stem from various causes, each...