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Published on: June 16, 2015
Collagenous vasculopathy: a report of three cases
Tracy L Davis1, Rajni V Mandal, Caroline Bevona
1Diagnostic Pathology Medical Group, Inc., Sacramento, CA, USA.
Insights
Cutaneous collagenous vasculopathy (CCV) is a rare microangiopathy affecting superficial blood vessels. This study identifies CCV in three additional Caucasian males, highlighting distinct histopathological features.
Area of Science:
- Dermatology
- Vascular Biology
- Histopathology
Background:
- Cutaneous collagenous vasculopathy (CCV) is a rare idiopathic microangiopathy.
- CCV involves superficial blood vessels and was initially reported in a single male patient.
Observation:
- Three additional Caucasian males with CCV were identified.
- Patients presented with asymptomatic, blanchable telangiectasias on the forearms, abdomen, chest, and thighs.
- Associated conditions included diabetes, hypertension, hypercholesterolemia, psoriasis, arthritis, and atrial fibrillation.
Findings:
- Histopathology revealed ectatic superficial small blood vessels.
- Distinctive laminated, hyalinized concretions around vessels were observed, highlighted by PAS staining and collagen type IV immunohistochemistry.
- CCV exhibits unique histopathological features differentiating it from generalized essential telangiectasia (GET).
Implications:
- CCV may affect a different demographic population than GET.
- Further research into this uncommon entity is needed to elucidate its etiology.
- Increased awareness of CCV can aid in diagnosis and understanding of microangiopathies.
Abstract:
Cutaneous collagenous vasculopathy (CCV) is an idiopathic microangiopathy involving the superficial blood vessels that was initially reported in a 54-year-old male. We recently have identified this rarely reported entity in three Caucasian males. The first patient was a 59-year-old male with diabetes, hypertension and hypercholesterolemia who presented with multiple, red, blanchable, asymptomatic telangiectasias covering the extensor surface of the forearms, the lower abdomen and parts of the chest. The second patient was a 62-year-old male with psoriasis and extensive arthritis who presented with prominent telangiectasias on the left lateral distal thigh with mild overlying epidermal atrophy. The third patient was an 80-year-old male with atrial fibrillation who presented with blanching, telangiectatic areas on the abdomen, thighs and back. Histologically, the skin lesions showed ectatic superficial small blood vessels with laminated, hyalinized concretions around vessels that were highlighted with periodic acid-Schiff staining following diastase digestion and reactive by immunohistochemical staining with an antibody to collagen type IV. CCV is a rare and poorly understood entity with distinct histopathological features that may clinically resemble generalized essential telangiectasia (GET), yet which may affect a different demographic population than GET. Awareness of this uncommon entity may further help to elucidate its etiology.
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