Lichen planus pigmentosus inversus (LPP-I) is characterized by the presence of hyperpigmented or hypopigmented lesions on the flexural surfaces of the body. It is a rare variant of lichen planus pigmentosus with unknown etiology. We report a case of a male presented with LPP-I three months after diagnosis of ocular myasthenia gravis, highlighting the possible autoimmune association.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10008231PMC
http://dx.doi.org/10.7759/cureus.34823DOI Listing

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