Pemphigus Foliaceus with Secondary Pseudomonas Aeruginosa Infection and Steroid-induced Hyperglycemia: a Case Report

Pemphigus foliaceus (PF) is a rare autoimmune blistering disorder caused by Immunoglobulin G (IgG) autoantibodies against desmoglein-1(Dsg-1), leading to superficial skin erosions without mucosal involvement. We report a case of a 71-year-old female who presented with flaccid blisters and crusted erosions over chest, back, neck, scalp, and face. A skin biopsy confirmed PF with subcorneal blister formation and Tzanck smear revealed acantholytic cells, supporting the diagnosis. She developed secondary Pseudomonas aeruginosa infection and steroid-induced hyperglycemia during treatment. Management included intravenous corticosteroids, targeted antibiotics, wound care, and monitoring of electrolytes and glucose levels. This case highlights the importance of early diagnosis, infection surveillance, and multidisciplinary care in PF to prevent complications and improve outcomes.

Authors

Publication Details

Journal
International Journal For Multidisciplinary Research
Published
2025-08-17
DOI
https://doi.org/10.36948/ijfmr.2025.v07i04.53941
Primary Topic
Autoimmune Bullous Skin Diseases
Type
article
Field-Weighted Citation Impact
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article

Pemphigus Foliaceus with Secondary Pseudomonas Aeruginosa Infection and Steroid-induced Hyperglycemia: a Case Report

Roshan Mathew, Alyssa Varghese, Lissy Skaria
International Journal For Multidisciplinary Research
Autoimmune Bullous Skin Diseases
article

Pemphigus Foliaceus with Secondary Pseudomonas Aeruginosa Infection and Steroid-induced Hyperglycemia: a Case Report

Roshan Mathew, Alyssa Varghese, Lissy Skaria
article en

Abstract

Pemphigus foliaceus (PF) is a rare autoimmune blistering disorder caused by Immunoglobulin G (IgG) autoantibodies against desmoglein-1(Dsg-1), leading to superficial skin erosions without mucosal involvement. We report a case of a 71-year-old female who presented with flaccid blisters and crusted erosions over chest, back, neck, scalp, and face. A skin biopsy confirmed PF with subcorneal blister formation and Tzanck smear revealed acantholytic cells, supporting the diagnosis. She developed secondary Pseudomonas aeruginosa infection and steroid-induced hyperglycemia during treatment. Management included intravenous corticosteroids, targeted antibiotics, wound care, and monitoring of electrolytes and glucose levels. This case highlights the importance of early diagnosis, infection surveillance, and multidisciplinary care in PF to prevent complications and improve outcomes.

International Journal For Multidisciplinary ResearchVol. 7(4)
Openalex Percentile: Top 69%
Autoimmune Bullous Skin Diseases
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