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Poikilodermatous Plaque-like Hemangioma: Case Presentation and Literature Review
Pablo Díaz-Calvillo1,2, Francisco Vílchez-Márquez1,2, Francisco Manuel Ramos-Pleguezuelos3
1Department of Dermatology, Hospital Universitario Virgen de las Nieves, Avenida de Madrid 15, 18012 Granada, Spain.
Abstract:
Poikilodermatous plaque-like hemangioma (PPH) is a recently described clinical and pathological entity, with only 18 cases reported in the literature. Although uncommon, this benign condition presents consistent clinical and histological findings. We present a new case of PPH in an 81-year-old male and review the existing literature. The persistence over time and the need to distinguish PPH from more significant lesions underscore the importance of its clinical and pathological recognition.
Insights
Poikilodermatous plaque-like hemangioma (PPH) is a rare benign skin condition. Recognizing PPH is crucial to differentiate it from more serious lesions due to its persistent nature.
Area of Science:
- Dermatology
- Pathology
Background:
- Poikilodermatous plaque-like hemangioma (PPH) is a recently identified clinical and pathological entity.
- Literature reports only 18 cases, highlighting its rarity.
Observation:
- Presents a case of PPH in an 81-year-old male.
- Reviews existing literature on PPH.
Findings:
- PPH exhibits consistent clinical and histological features despite its rarity.
- The condition is benign.
Implications:
- Emphasizes the importance of accurate clinical and pathological recognition of PPH.
- Distinguishing PPH from potentially malignant lesions is critical for patient management.
