Lichen Planus Pemphigoides: A Clinical, Histopathological, and Immunological Report of 12 Indian Patients
LPP is a rare subepidermal blistering disorder seen more commonly in adult females. DIF, ELISA, and salt-split indirect immunofluorescence are helpful tools in confirming the diagnosis of LPP and differentiating from bullous lichen planus. Oral corticosteroids comprised the mainstay of therapy. Azathioprine or dapsone were commonly used adjuvants.
Authors
- Rahul Mahajan (ORCID: https://orcid.org/0000-0003-4320-3193)
- Dipankar De (ORCID: https://orcid.org/0000-0001-8682-2598)
- Akash P. Mustari (ORCID: https://orcid.org/0000-0002-8224-0221)
- Vinod Kumar (ORCID: https://orcid.org/0000-0003-3733-4197)
- Sanjeev Handa
- Debajyoti Chatterjee
Institutions
- Post Graduate Institute of Medical Education and Research (IN)
Publication Details
- Journal
- Indian Dermatology Online Journal
- Published
- 2025-05-26
- DOI
- https://doi.org/10.4103/idoj.idoj_763_24
- Citations
- 1
- Primary Topic
- Autoimmune Bullous Skin Diseases
- Type
- article
- Field-Weighted Citation Impact
- 1.47