Hyperkeratotic cutaneous capillary-venous malformation

Hyperkeratotic cutaneous capillary-venous malformation
Synonyms	HCCVM
Pronounce	N/A
Specialty	N/A
Symptoms	Hyperkeratosis, capillary malformation, venous malformation
Complications	Pain, bleeding, infection
Onset	Childhood
Duration	Chronic
Types	N/A
Causes	Genetic mutation
Risks	Family history
Diagnosis	Clinical examination, skin biopsy, imaging studies
Differential diagnosis	Port-wine stain, venous malformation, arteriovenous malformation
Prevention	N/A
Treatment	Laser therapy, sclerotherapy, surgical excision
Medication	N/A
Prognosis	Variable, depends on size and location
Frequency	Rare
Deaths	N/A

Hyperkeratotic Cutaneous Capillary-Venous Malformation (HCCVM) is a rare skin disorder characterized by the presence of capillary-venous malformations that are associated with a hyperkeratotic surface. These malformations are a type of vascular anomaly that affects the blood vessels in the skin, leading to distinctive skin changes.

Overview

HCCVM is considered a rare condition and is part of a broader category of vascular anomalies, which include a wide range of vascular tumors and malformations. Unlike more common vascular anomalies, such as simple hemangiomas, HCCVMs are notable for their hyperkeratotic (thickened skin) surface, which can make diagnosis and treatment more challenging.

Causes

The exact cause of HCCVM is not fully understood, but it is believed to involve genetic mutations that affect the development and growth of blood vessels. These mutations may be sporadic or, in rare cases, inherited. The condition is characterized by an abnormal connection between capillaries (the smallest blood vessels) and veins, leading to the malformation.

Symptoms

Symptoms of HCCVM include:

• Visible capillary-venous malformations on the skin, which may appear as red to purple patches or lesions.
• Hyperkeratosis over the lesions, giving them a rough, thickened texture.
• Possible discomfort or pain in the affected area.
• In some cases, bleeding or ulceration of the lesions may occur.

Diagnosis

Diagnosis of HCCVM typically involves a combination of clinical examination and imaging studies. Dermoscopy and magnetic resonance imaging (MRI) can be particularly useful in assessing the extent of the malformation and its impact on surrounding tissues. Biopsy of the lesion may also be performed to confirm the diagnosis and rule out other conditions.

Treatment

Treatment options for HCCVM are limited and focus primarily on managing symptoms and preventing complications. Options may include:

• Topical treatments to reduce hyperkeratosis and improve skin texture.
• Laser therapy to reduce the visibility of the malformations.
• Surgical removal in cases where the malformation causes significant discomfort or is cosmetically concerning.

Prognosis

The prognosis for individuals with HCCVM varies depending on the size and location of the malformation, as well as the presence of any complications. While the condition itself is not life-threatening, it can impact quality of life due to cosmetic concerns or discomfort.

See Also

• Vascular anomaly
• Hemangioma
• Skin disorder

   This article is a medical stub. You can help WikiMD by expanding it!