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Reticulate Acropigmentation of Dohi
*Corresponding author: Logamoorthy Ramamoorthy, Department of Dermatology, JIPMER, Puducherry, India. logamoorthy.r@gmail.com
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Received: ,
Accepted: ,
How to cite this article: Ramamoorthy L, Singh D. Reticulate Acropigmentation of Dohi. Indian J Postgrad Dermatol 2023;1:142-3.
A 15-year-old boy presented with complaints of asymptomatic hypo and hyperpigmented spots over dorsa of the hands and feet since birth. There was family history of similar complaints in father and paternal grandfather in the same distribution. There was no history of photosensitivity, photophobia or darkening of the lesions on sun exposure. On cutaneous examination, multiple hypo and hyperpigmented macules were present in symmetrical distribution over dorsum of both hands and feet. There were multiple freckles on his face. There were no palmar pits and his mucosae were normal [Figure 1]. The patient’s intelligence was normal and his systemic examination revealed no abnormality. Based on history and clinical examination [Figure 2], a diagnosis of reticulate acropigmentation of Dohi was made. Acropigmentation of Dohi has to be differentiated from other pigmentary disorders such as reticulate pigmentation of Kitamura and Dowling–Degos disease.[1] We present this case due to its rare occurrence. Identifying and differentiating the condition from other pigmentary dermatoses is important for appropriate counselling and prognostication.
Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent.
Conflicts of interest
There are no conflicts of interest.
Financial support and sponsorship
Nil.
References
- Reticulate acropigmentation of dohi: A case report with insight into genodermatoses with mottled pigmentation. Indian J Dermatol. 2012;57:42-4.
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