“…Histopathologically, sub-epithelial fibrin deposition was the most common histological description with 23.7% cases [15,16,19,21,26,31,32,35,40], interestingly only described in females, followed by epithelial disorganization and amyloid like material, and acute and chronic inflammation [9,10,14,20,23,31] seen in both sexes with 18.4% (n=7) of cases; this is an important fact to mention, according to Günhan Ö et al in 2012, there are histological early and late changes of ligneous disease, where PMN exudation, immunoreactivity to fibrinogen, keratin positivity and amorphous accumulation, occurs at early stage principally, and sub-epithelial amorphous accumulation occurs at late stage with chronic inflammation cells [13] (Figure 2). This is key to allow accuracy in the diagnosis, where the differentiation between amyloid and other proteins like fibrin, with a similar histologic appearance [29], could be excluded with a Congo red positively for amyloid and using special stains such as Fibrin and MSB to confirm fibrin deposition, which in this study was found in 22.4% of the cases [1,9,10,38].…”