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Poikilodermatous plaque-like hemangioma: Case series of a newly defined entity
Kristina Semkova1, Richard Carr2, Mark Grainger3
1Department of Dermatopathology, St. John's Institute of Dermatology, Guys and St Thomas' Foundation Trust, London, England.
Background:
We present a distinctive type of acquired vascular proliferation, for which we propose the name of poikilodermatous plaque-like hemangioma.
Objective:
The aim of this study was to summarize the clinical and histopathologic features in a case series of poikilodermatous plaque-like hemangioma.
Methods:
Sixteen cases were identified from the routine clinical and referral practices of the authors. Clinical characteristics, including demographic details and clinical morphology, were collated. The salient histopathologic features, including immunohistochemical staining results, were summarized.
Results:
The lesions were usually solitary erythematous-to-violaceous poikilodermatous plaques on the lower extremities and pelvic girdle, with an indolent clinical course. Mean age of affected patients was 72 (range 58-80) years, and there was a male predominance. Histology comprised a distinctive band-like proliferation of vascular channels suggestive of postcapillary venules within the superficial dermis with a background of fibrosis, edema, and loss of elastic fibers. Despite the clinical atrophic appearance, acanthosis was a frequent finding.
Limitations:
Retrospective study.
Conclusion:
Poikilodermatous plaque-like hemangioma is a distinctive and previously undescribed vascular proliferation defined by a constellation of consistent and reproducible clinical and histologic features.
Insights
A new vascular skin condition, poikilodermatous plaque-like hemangioma, is described. This acquired condition presents as distinct plaques with specific clinical and histological features.
Area of Science:
- Dermatology
- Pathology
- Vascular Biology
Background:
- Presents a novel vascular proliferation termed poikilodermatous plaque-like hemangioma.
- This condition is acquired and characterized by unique clinical and histological findings.
Purpose of the Study:
- To summarize the clinical and histopathologic features of poikilodermatous plaque-like hemangioma.
- To define this previously undescribed vascular proliferation.
Main Methods:
- Retrospective case series analysis of 16 patients.
- Collated clinical characteristics including demographics and morphology.
- Summarized histopathologic features and immunohistochemical results.
Main Results:
- Lesions typically appeared as solitary, erythematous-to-violaceous, poikilodermatous plaques on lower extremities and pelvic girdle.
- Affected patients had a mean age of 72 years, with a male predominance and an indolent clinical course.
- Histology revealed band-like vascular proliferation (postcapillary venules) in the superficial dermis, accompanied by fibrosis, edema, and elastic fiber loss; acanthosis was common despite an atrophic appearance.
Conclusions:
- Poikilodermatous plaque-like hemangioma is a distinct, previously undescribed vascular proliferation.
- The condition is defined by a consistent set of clinical and histological features.
- Further research may elucidate the pathogenesis and optimal management.
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