Reticulate hypopigmentation of Dohi: a characteristic patterned pigmentary disorder: a rare clinical image
Garima Gupta, Shweta Parwe
Corresponding author: Shweta Parwe, Department of Panchkarma, Mahatma Gandhi Ayurveda College Hospital and Research Centre, Salod (Hirapur), Datta Meghe Institute of Higher Education and Research, Wardha, Maharashtra, India 
Received: 05 Dec 2025 - Accepted: 29 Dec 2025 - Published: 10 Feb 2026
Domain: Dermatology,Internal medicine
Keywords: Reticulate hypopigmentation of Dohi, dyschromatosis, genodermatosis, hypopigmented macules
Funding: This work received no specific grant from any funding agency in the public, commercial, or non-profit sectors.
©Garima Gupta 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: Garima Gupta et al. Reticulate hypopigmentation of Dohi: a characteristic patterned pigmentary disorder: a rare clinical image. Pan African Medical Journal. 2026;53:76. [doi: 10.11604/pamj.2026.53.76.50495]
Available online at: https://www.panafrican-med-journal.com//content/article/53/76/full
Images in clinical medicine 
Reticulate hypopigmentation of Dohi: a characteristic patterned pigmentary disorder: a rare clinical image
Reticulate hypopigmentation of Dohi: a characteristic patterned pigmentary disorder: a rare clinical image
&Corresponding author
A 23-year-old male presented with asymptomatic hypopigmented lesions over the dorsal aspects of the hands, feet, and neck, noticed since early childhood. The lesions were non-progressive and symmetrically distributed. Cutaneous examination revealed multiple, well-defined, reticulate hypopigmented macules over the acral regions without associated erythema, scaling, or atrophy. No involvement of the trunk, face, hair, nails, or mucosa was noted. There was no significant past medical history. The diagnostic approach was based on the characteristic acral distribution, reticulate pattern of hypopigmentation, early onset, and absence of inflammatory changes, which are typical features of reticulate hypopigmentation of Dohi, a rare inherited pigmentary disorder. The patient was counselled regarding the benign nature of the condition, and reassurance was provided. No active medical treatment was initiated. At short-term follow-up, the lesions remained stable without progression.
Figure 1: A) reticulate hypopigmented macules over the lateral neck; B) symmetrical reticulate hypopigmented macules over the dorsal hands and feet



