# The Changing Trends in the Incidence and Clinical Presentation of Immunobullous Disorders Before and During the COVID-19 Era in a Tertiary Healthcare Centre in Andhra Pradesh

**Authors:** Pooja Unnikrishnan, Jami Vijayashree, Dilipchandra Chintada, Mohammed Khatija Begum, Pallavi Gullipalli, Sai Sriya Chalamalasetty

PMC · DOI: 10.7759/cureus.101337 · Cureus · 2026-01-12

## TL;DR

This study found that autoimmune blistering skin diseases increased during the COVID-19 era, with younger patients and more complex symptoms requiring advanced diagnosis.

## Contribution

The study identifies novel clinical trends in immunobullous disorders during the pandemic, including younger onset and atypical presentations requiring diagnostic confirmation.

## Key findings

- A 57.1% increase in AIBD incidence was observed during the COVID era.
- Atypical clinical patterns emerged, requiring histopathology and DIF for diagnosis.
- Mucosal involvement and recurrence rates increased during the pandemic period.

## Abstract

Background

Autoimmune immunobullous disorders (AIBDs) represent a heterogeneous group of chronic blistering dermatoses mediated by autoantibodies against desmosomal and hemidesmosomal adhesion molecules. The COVID-19 pandemic has generated significant interest in the interaction between SARS-CoV-2 infection, vaccination-related immune modulation, and the clinical behaviour of autoimmune diseases.

Objective

This study’s primary objective is to compare hospital-based temporal trends in the frequency, subtype distribution, and clinical presentation of AIBDs before and during the COVID-19 era in a tertiary healthcare centre in Andhra Pradesh. Secondary objectives included evaluation of changes in age at onset, sex distribution, mucosal and nail involvement, recurrence, and the emergence of atypical clinical morphologies requiring histopathology and direct immunofluorescence (DIF) for definitive diagnosis, as well as identification of independent predictors of subepidermal AIBD subtypes using multivariate logistic regression.

Methods

A retrospective observational analysis was performed on 42 histopathology and/or DIF-confirmed AIBD cases. Eighteen cases were recorded in the pre-COVID period (January 2018-December 2019) and 24 during the COVID era (January 2020-November 2023). Demographic trends, morphological patterns, mucosal involvement, anatomical distribution, severity, recurrence, and atypical phenotypes were compared between the two cohorts.

Results

A notable increase in overall incidence was observed during the COVID era (57.1%). Disease onset occurred at a younger age during COVID (mean 47.8 years) compared with the pre-COVID period (mean 53.6 years). Mucosal involvement increased from 33.3% pre-COVID to 50% during COVID. The COVID cohort exhibited higher recurrence rates and atypical morphology, including confluent mucosal and oesophageal lesions in epidermolysis bullosa acquisita, a “cluster of jewels” configuration and nail dystrophy in bullous pemphigoid, and healing with scarring and milia. These atypical patterns required more frequent reliance on biopsy and DIF for achieving a definitive diagnosis, as classical clinical presentation alone was insufficient.

Conclusion

The COVID-19 era was associated with both increased hospital-based case frequency and altered clinical expression of AIBDs, characterised by younger disease onset, greater mucosal involvement, and diagnostically challenging phenotypes. Possible contributors include post-COVID immune dysregulation, vaccination-associated immune activation, psychological stress, and lifestyle changes. Intensified clinical vigilance, early DIF-based confirmation, and timely initiation of steroid-sparing immunomodulatory therapy are essential to optimise outcomes in the evolving post-pandemic context.

## Linked entities

- **Diseases:** SARS-CoV-2 (MONDO:0100096), epidermolysis bullosa acquisita (MONDO:0018747), bullous pemphigoid (MONDO:0019082)

## Full-text entities

- **Diseases:** COVID (MESH:D000086382), epidermolysis bullosa acquisita (MESH:D016107), blistering dermatoses (MESH:D001768), nail dystrophy (MESH:D009260), immune dysregulation (OMIM:614878), chronic (MESH:D002908), post-COVID (MESH:D000094024), Mucosal involvement (MESH:D052016), bullous pemphigoid (MESH:D010391), oesophageal lesions (MESH:D000077277), Immunobullous Disorders (MESH:D009358), AIBDs (MESH:D001327)
- **Chemicals:** steroid (MESH:D013256)

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12894093/full.md

## References

20 references — full list in the complete paper: https://tomesphere.com/paper/PMC12894093/full.md

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Source: https://tomesphere.com/paper/PMC12894093