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Summary
This case report details lichen purpuricus, a rare skin condition. Histopathology revealed a dense dermal infiltrate and hemosiderin, aiding diagnosis when clinical presentation was unclear.
Area of Science:
- Dermatology
- Histopathology
Background:
- Lichen purpuricus is a rare dermatosis with variable clinical presentations.
- Accurate diagnosis can be challenging based on clinical examination alone.
Observation:
- A 19-year-old male presented with a recurrent eruption of asymptomatic, dark-red macules and papules on his left hand.
- The eruption had resolved spontaneously before reappearing, complicating initial clinical diagnosis.
Findings:
- Histopathological examination revealed a dense, band-like infiltrate in the upper dermis.
- The infiltrate consisted of lymphocytes, histiocytes, and extravasated red blood cells, with hemosiderin granules present.
Implications:
- Histopathological findings are crucial for diagnosing lichen purpuricus when clinical features are ambiguous.
- This case contributes to understanding the clinical and histopathological spectrum of lichen purpuricus.