Schamberg’s Disease: A Rare Case Report from a Tertiary Care Hospital in Gujarat

Pigmented purpuric dermatoses (PPDs) comprise a collection of disorders characterized by many petechial hemorrhages due to underlying capillaritis. Specific clinical characteristics facilitate the categorization of PPD into different variants, with Schamberg's disease being the most frequently encountered. Treatment may not always yield positive results, and recurrences are common. We report the case of a 38-year-old male patient who presented with numerous reddish lesions on his lower and upper limbs, as well as his trunk. He exhibited purpuric eruptions and brownish discolorations that were diffusely spread across these areas. A biopsy indicated Schamberg's disease. The patient was treated with oral anti-inflammatory drugs. After 3 months of follow-up, there was significant improvement in the existing lesions, and no new lesions had developed.