Here, in this case, congo red stain was used for a definite diagnosis of ACD.[[12]] Various treatment modalities have been described for the treatment of ACD with varying success rates. The clinical, histopathological and treatment profile of these published cases of ACD has been compiled in [Table 1].[[4]],[[5]],[[6]],[[7]],[[8]],[[9]],[[10]]{Table 1} ACD must be differentiated from other causes of dyschromia including dyschromatosis universalis hereditaria, xeroderma pigmentosum and poikiloderma-like amyloidosis. Sir, In 1970, Morishima et al. introduced amyloidosis cutis dyschromica (ACD), a rare variant of primary cutaneous amyloidosis (PCA). [Extracted from the article]