Extensive cutaneous involvement in pemphigus vulgaris in a pediatric patient: a rare clinical image
Sahil Vihirkar, Darshana Kumari Wankhede
Corresponding author: Sahil Vihirkar, Department of Child Health Nursing, Smt. Radhikabai Meghe Memorial College of Nursing Sawangi (Meghe), Datta Meghe Institute of Higher Education and Research, Sawangi (Meghe), Wardha, Maharashtra, India 
Received: 11 Oct 2025 - Accepted: 19 Oct 2025 - Published: 16 Jan 2026
Domain: Nursing education,Public Health Nursing,Pediatrics (general)
Keywords: Pemphigus vulgaris, pediatrics, autoimmune blistering disease, skin
Funding: This work received no specific grant from any funding agency in the public, commercial, or non-profit sectors.
©Sahil Vihirkar et al. Pan African Medical Journal (ISSN: 1937-8688). This is an Open Access article distributed under the terms of the Creative Commons Attribution International 4.0 License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Cite this article: Sahil Vihirkar et al. Extensive cutaneous involvement in pemphigus vulgaris in a pediatric patient: a rare clinical image. Pan African Medical Journal. 2026;53:19. [doi: 10.11604/pamj.2026.53.19.49727]
Available online at: https://www.panafrican-med-journal.com//content/article/53/19/full
Images in clinical medicine 
Extensive cutaneous involvement in pemphigus vulgaris in a pediatric patient: a rare clinical image
Extensive cutaneous involvement in pemphigus vulgaris in a pediatric patient: a rare clinical image
&Corresponding author
A 4-year-old child presented with multiple hyperpigmented and hypopigmented macules and plaques over both forearms, with a history of recurrent flaccid bullae and erosions at the same sites. Nikolsky sign was positive during the active phase. Tzanck smear showed acantholytic cells, and skin biopsy revealed intraepidermal acantholysis. Direct immunofluorescence demonstrated intercellular deposition of IgG and C3 in a fish-net pattern, confirming the diagnosis. The child was treated with systemic corticosteroids and azathioprine, leading to disease control. The present image shows the healing phase with post-inflammatory dyspigmentation and residual scarring, highlighting chronic sequelae of pediatric pemphigus vulgaris, a rare condition in this age group.
Figure 1: A) healed hyperpigmented and hypopigmented plaques over both forearms in a pediatric patient with a known history of pemphigus vulgaris; B) multiple hypopigmented and scarring lesions over the back in a child with previously treated tinea corporis (dermatophytosis)



