Vascular Anomalies
Vascular anomalies are conditions that affect how your child’s arteries, veins, lymphatic vessels, or capillaries develop. Some are first noticed on a prenatal ultrasound, while others appear in infancy or early childhood. These conditions can range from simple birthmarks to complex malformations that affect blood flow or organ function.
Vascular anomalies symptoms
Vascular anomalies can look and behave differently depending on the vessel involved. You should contact your care team if you notice any of the following symptoms:
- Skin discoloration or visible markings
- Soft or firm masses under the skin
- Swelling in a limb or part of the body
- Rapidly growing lesions in infancy
- Breathing or feeding concerns
How vascular anomalies are diagnosed
Your child’s evaluation may begin even before birth through our fetal cardiology program, which uses advanced imaging to assess heart structure and blood flow. After birth, if symptoms appear, your child’s care team will review their health history, symptoms, and perform a thorough physical examination. They may also order diagnostic tests such as:
Our specialists will explain every step in clear, supportive language, so you understand what the findings mean and what to expect next.
Pediatric vascular anomaly treatment
Treatment depends on the type and severity of the anomaly. Many mild conditions only require monitoring, while others benefit from medication, procedures, or surgery. We tailor every plan to your child’s needs.
Some vascular anomalies simply need time and a careful watch. We track growth and symptoms and guide you on what to look for at home.
Certain anomalies — such as infantile hemangiomas — respond well to medications like beta-blockers, which can slow or shrink the growth
Laser treatment can improve the appearance or symptoms of skin-based vascular anomalies such as port-wine stains.
Our specialists use minimally invasive options such as sclerotherapy or embolization to reduce or block abnormal blood flow.
Surgery may be recommended for anomalies that cause symptoms, affect organ function, or don’t respond to other therapies. Our surgeons work closely with cardiology and imaging to plan the safest approach.
Coordinated, multidisciplinary care
Because vascular anomalies can affect breathing, feeding, circulation, or a child’s overall development, we bring together the right specialists at every stage of care. Our multidisciplinary team may include experts from otolaryngology, dermatology, oncology, cardiology, and pediatric surgery, ensuring your child receives comprehensive, well‑coordinated evaluation and treatment.
Support services for vascular anomalies
We know your family needs support beyond medical care. That’s why you have access to child life services, social work, nutrition guidance, and genetic counseling when appropriate. We’ll also help coordinate follow-up appointments and connect you with additional specialists as needed.
A collaborative approach to care
Your child’s care begins with a thorough evaluation by a pediatric cardiology, fetal cardiology, or vascular anomalies specialist. We review imaging together, explain the diagnosis in clear terms, and outline next steps. You’ll have a coordinated team guiding you from diagnosis to treatment and follow-up, with specialists collaborating behind the scenes to provide your child with the safest, most comprehensive care.
Common questions about vascular anomalies
Most pediatric vascular anomalies are congenital and not caused by anything a parent does during pregnancy. They often occur due to genetic changes that happen spontaneously.
Some do. Early evaluation helps us predict how an anomaly may behave and whether treatment is recommended now or later.
Our Care Team
Our providers specialize in diagnosing and treating vascular anomalies in infants, children, and adolescents.
Need help finding a vascular anomalies specialist?
Locations and Offices
Patient Stories
Support Groups
Heart Friends supports parents, siblings, and caregivers of children with congenital or acquired heart disease. A child’s heart condition is more than a medical experience. It affects every aspect of family life. Heart Friends gives you a community of families who truly understand, helping you find emotional support, educational tools, and social connections when it matters most.
What is Heart Friends?
Heart Friends is a statewide network for families receiving cardiac care at University of Iowa Health Care Stead Family Children’s Hospital, with chapters across Iowa.
With a mission to provide emotional and educational support, raise awareness of congenital heart disease, and build a strong community for families at every stage of the heart-care journey, Heart Friends offers:
- Emotional support and mentoring through peer connection with other families who have walked similar paths.
- Educational events that give you reliable information about congenital heart defects, treatments, and long-term care.
- Social gatherings and chapter events so your children and your family can meet others and just have fun.
All families have different needs, so we allow you to join at any point in your child's heart journey when you are ready to share with others. What we do is create connection, awareness, and a place where you feel heard and understood.
When to join Heart Friends
You may find Heart Friends helpful:
- When your child is newly diagnosed with a heart condition, and you’re looking for support and guidance.
- When you’re facing surgery or complex care and want families who’ve been there.
- When you’re feeling isolated, want to connect with other siblings or caregivers, or need educational resources.
- Even when your child is stable, but you want to join a community with social events and children’s activities with peers who understand.
If at any point in your heart-care journey you feel you’d benefit from connection, reassurance, or resources — it’s a good time to join.
What to expect
When you become part of Heart Friends, you’ll have access to:
- Chapters in multiple regions (UIHC, Dubuque chapter, Waterloo chapter and Central Iowa chapter) with local event invitations.
- Welcome materials and social media options
- Social gatherings (annual CHD Day events, sporting events, family events, parent events, and more!) where you and your children can meet others.
- Opportunities to volunteer or support awareness efforts if you’d like to give back.
Our program allows you to participate at your own pace and according to what your family needs.
Donate to Heart Friends
We are grateful for the many generous individuals and organizations who wish to bring cheer and comfort to our young patients and their families. You often ask how you can help. The biggest impact you can make is through a monetary donation to the Stead Family Children’s Hospital Fund. This fund provides support for the most urgent needs of Stead Family Children’s Hospital.
Give now
Heart Friends Support Group Contacts
UI Health Care Chapter
Trudy Pierick
[email protected]
Dubuque Chapter
Jesi Duve
[email protected]
Lindsey Schueller
[email protected]
Waterloo Chapter
Molly Burns
[email protected]
Kris Messner
[email protected]
Central Iowa Chapter
Brittany Devereaux
[email protected]
Autumn Wolbert
[email protected]
Awards and Recognition