Pemphigus Vulgaris Unveiled: From Nikolsky's Sign to Immunofluorescence

Abstract Oral pemphigus vulgaris (PV) is a rare, chronic, autoimmune, mucocutaneous disorder characterized by the formation of flaccid blisters and painful erosions, predominantly affecting the oral mucosa. This case report describes a 52-year-old female presenting with ulcerations in the buccal mucosa as well as alveolar mucosa, accompanied by a positive Nikolsky’s sign. Diagnostic investigations including cytology, histopathology, and direct immunofluorescence, confirmed the diagnosis of PV, revealing characteristic features such as suprabasilar split, Tzanck cells, and a “fish-net” pattern of IgG deposition. Early diagnosis and initiation of systemic corticosteroids and immunosuppressive therapy are crucial in reducing morbidity and preventing complications. This report, emphasizes the importance of early recognition, particularly by dental professionals, and highlight the advances in treatment strategies including the role of therapeutic agents like rituximab, in improving patient outcomes.

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Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2025-07-30
DOI
https://doi.org/10.5281/zenodo.18067111
Primary Topic
Autoimmune Bullous Skin Diseases
Type
article
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article

Pemphigus Vulgaris Unveiled: From Nikolsky's Sign to Immunofluorescence

International Journal of Medical Science and Innovative Research (IJMSIR)
Zenodo (CERN European Organization for Nuclear Research)
Autoimmune Bullous Skin Diseases
article

Pemphigus Vulgaris Unveiled: From Nikolsky's Sign to Immunofluorescence

International Journal of Medical Science and Innovative Research (IJMSIR)
article en

Abstract

Abstract Oral pemphigus vulgaris (PV) is a rare, chronic, autoimmune, mucocutaneous disorder characterized by the formation of flaccid blisters and painful erosions, predominantly affecting the oral mucosa. This case report describes a 52-year-old female presenting with ulcerations in the buccal mucosa as well as alveolar mucosa, accompanied by a positive Nikolsky’s sign. Diagnostic investigations including cytology, histopathology, and direct immunofluorescence, confirmed the diagnosis of PV, revealing characteristic features such as suprabasilar split, Tzanck cells, and a “fish-net” pattern of IgG deposition. Early diagnosis and initiation of systemic corticosteroids and immunosuppressive therapy are crucial in reducing morbidity and preventing complications. This report, emphasizes the importance of early recognition, particularly by dental professionals, and highlight the advances in treatment strategies including the role of therapeutic agents like rituximab, in improving patient outcomes.

Zenodo (CERN European Organization for Nuclear Research)
Innovative Research (United States) (US)
Openalex Percentile: Top 29%
Autoimmune Bullous Skin Diseases
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