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Nephrotic Syndrome I : Introduction

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Nephrotic Syndrome is a chronic kidney disorder defined by clinical findings such as severe proteinuria, hypoalbuminemia, hyperlipidemia, and edema. These symptoms result from damage to the glomeruli, the kidney’s filtering units, increasing their permeability to proteins.Definition and Meaning:Proteinuria, defined as the loss of more than 3.5 grams of protein per day in adults, is a crucial feature of nephrotic syndrome. This condition is often accompanied by edema, the accumulation of...
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Prostacyclin receptor agonists are a class of therapeutic agents integral to managing pulmonary arterial hypertension (PAH). These drugs operate by mimicking the action of prostaglandin I2, or PGI2, a naturally occurring compound in the body.
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Peptic Ulcer Disease I: Introduction01:30

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Peptic Ulcer Disease (PUD) is characterized by mucosal excavation in the esophagus, stomach, pylorus, or duodenum. It can manifest as acute or chronic based on the extent and duration of mucosal involvement.
An acute ulcer, marked by superficial erosion and minimal inflammation, swiftly resolves upon identifying and addressing the underlying cause. In contrast, a chronic ulcer persists, potentially eroding through the muscular wall and forming fibrous tissue.
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Treatment for Pulmonary Arterial Hypertension: Endothelin Receptor Antagonists01:18

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Endothelins (ETs) are potent vasoactive peptides critical in the human body's various physiological and pathological processes. One of the most promising therapeutic strategies for treating pulmonary arterial hypertension (PAH) involves counteracting the effects of these endothelins using a class of drugs known as endothelin receptor antagonists.
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Gastritis-II: Pathophysiology01:17

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Gastritis is marked by disruption of the mucosal barrier that usually protects the stomach tissue from digestive juices and manifests in acute and chronic forms.
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Eosinophilic Granulomatosis with Polyangiitis.

Ratnakar Shukla1, Ashwini Kandikatla2, Nitin J Nadkarni3

  • 1Department of Dermatology, All India Institute of Medical Sciences, Gorakhpur, Uttar Pradesh, India.

International Journal of Applied & Basic Medical Research
|June 27, 2022
PubMed
Summary

This report details a rare case of Eosinophilic Granulomatosis with Polyangiitis (EGPA), also known as Churg-Strauss syndrome, in a 58-year-old male. The patient presented with lower limb swelling and skin lesions, highlighting EGPA

Area of Science:

  • Rheumatology
  • Immunology
  • Dermatology

Background:

  • Eosinophilic Granulomatosis with Polyangiitis (EGPA), or Churg-Strauss syndrome, is a rare systemic necrotizing vasculitis affecting small-to-medium-sized vessels.
Keywords:
Churg–Strauss syndromeP-antineutrophil cytoplasmic antibodyeosinophiliaeosinophilic granulomatosis with polyangiitis

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  • EGPA is characterized by asthma, hypereosinophilia, and systemic vasculitis.