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Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease
Published on: June 16, 2020
The gastric wall in systemic sclerosis patients: a morphological study.
Mirko Manetti1, Anna Franca Milia, Gemma Benelli
1Department of Anatomy, Histology and Forensic Medicine, University of Florence, Florence, Italy.
Summary
Systemic sclerosis causes organ failure due to fibrosis. In affected patients, gastric wall fibrosis and ultrastructural damage to smooth muscle and nerve cells are key histopathological findings.
Area of Science:
- Gastroenterology
- Rheumatology
- Pathology
Background:
- Systemic sclerosis (SSc) is a multisystem autoimmune disease characterized by fibrosis.
- Gastrointestinal dysmotility is a common and severe manifestation of SSc, impacting patient morbidity and mortality.
- Gastric involvement in SSc can lead to severe gastroesophageal dysfunction requiring surgical intervention.
Purpose of the Study:
- To investigate the histopathological changes in the gastric wall of patients with systemic sclerosis and severe gastroesophageal involvement.
- To evaluate the ultrastructural alterations in smooth muscle cells and nerve fibers within the gastric wall.
Main Methods:
- Analysis of full-thickness gastric biopsies from SSc patients undergoing surgery.
- Histopathological examination using light microscopy and transmission electron microscopy.
Main Results:
- Generalized fibrosis was observed throughout all layers of the gastric wall, with pronounced changes in the muscularis mucosae and muscle layers.
- Smooth muscle cells exhibited disarranged or absent myofilaments and thickened dense bodies.
- Nerve fibers showed ultrastructural alterations, including oedematous axoplasm and reduced cytoskeletal elements, ensheathed by abundant collagen and elastic fibers.
- Interstitial cells of Cajal were also enveloped by connective tissue, potentially disrupting cell-to-cell communication.
Conclusions:
- Prominent fibrosis and severe ultrastructural alterations of smooth muscle and nerve components are the primary histopathological hallmarks in the gastric wall of systemic sclerosis patients.
- These findings contribute to understanding the pathophysiology of SSc-associated gastrointestinal dysmotility.
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