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Angiokeratoma corporis diffusum (ACD) is a rare clinical type of angiokeratoma and has been reported, mostly, in association with various life threatening conditions, of which Fabry disease is the most known. Rarely, it has been reported as an isolated finding without any systemic features. A 23-year-old male presented with numerous red papules of various sizes with a history of intermittent bleeding. Histopathology findings were consistent with angiokeratoma and our case was diagnosed as ACD. We herein present a case of cutaneous variant of ACD without any associated systemic associations. Also, the conditions associated with ACD have been briefly discussed. [ABSTRACT FROM AUTHOR]

Inverse (flexural) psoriasis is characterized by shiny, pink to red, sharply-demarcated thin plaques. Frequency of isolated involvement of these areas is very rare and the morphology is frequently altered by maceration and friction. All this leads to diagnostic confusion. We describe two cases of inverse psoriasis with isolated involvement of axillae. One patient presented with dry mildly scaly plaque, while the other presented with macerated plaque. Histopathology was consistent with the diagnosis of inverse psoriasis. Although there are previous reports, but localization of lesions only to axillae in a case of inverse psoriasis is unique. [ABSTRACT FROM AUTHOR]

The article discusses the case of a man with a solitary painful mass on his chest diagnosed as eccrine spiradenoma. A description of the lesion and nodule, the patient's history, and the mass and epithelial cords found under histopathological examination are presented. The nine unique tumors to be considered when diagnosing painful skin tumors, the occurrence of spiradenomas in Brooke-Spiegler syndrome, and the treatment option are discussed.