Congenital phlebectasia digital illustration

Congenital phlebectasia Save


ICD-10 code: Q27.4

Chapter: Congenital malformations, deformations and chromosomal abnormalities

Congenital Phlebectasia: A Rare Vascular Abnormality

Congenital phlebectasia, also known as blue rubber bleb nevus syndrome, is a rare vascular abnormality that affects the veins and capillaries. It is a non-hereditary disorder that is usually present at birth or appears in early childhood. The condition is characterized by the formation of multiple, small, blue or purple lesions on the skin and internal organs. These lesions are made up of dilated veins and can cause a variety of symptoms depending on their location.

  1. Symptoms: The symptoms of congenital phlebectasia can vary depending on the location and size of the lesions. The most common symptoms include:
    • Blue or purple lesions on the skin
    • Bleeding from the lesions
    • Pain or discomfort in the affected area
    • Swelling or inflammation
    • Gastrointestinal bleeding
  2. Cause: The exact cause of congenital phlebectasia is unknown. However, researchers believe that it may be caused by a genetic mutation that affects the development of the veins and capillaries. The condition is not hereditary, but it can occur in multiple members of the same family.
  3. Treatment: There is no cure for congenital phlebectasia. Treatment is focused on managing the symptoms and preventing complications. In some cases, surgery may be necessary to remove the lesions or control bleeding. Medications, such as corticosteroids, may also be prescribed to reduce inflammation and pain.
  4. Prognosis: The prognosis for individuals with congenital phlebectasia varies depending on the severity and location of the lesions. In most cases, the condition is not life-threatening. However, complications such as gastrointestinal bleeding or thrombosis can be serious and require immediate medical attention.
  5. Prevention: There is no known way to prevent congenital phlebectasia. However, individuals with a family history of the condition may benefit from genetic counseling to assess their risk.

Congenital phlebectasia is a rare but serious condition that requires ongoing medical management. If you or a loved one is experiencing symptoms of this disorder, it is important to seek medical attention promptly. With proper treatment, the symptoms of congenital phlebectasia can be managed and complications can be prevented.

Diagnosis Codes for Congenital phlebectasia | Q27.4