Port-wine stain or infantile hemangioma: how to tell them apart
Two common vascular birthmarks that look similar but behave very differently. One persists and is treated with laser, the other usually grows then fades.

Port-wine stain and infantile hemangioma are the two most common vascular birthmarks in children. They can look similar to a worried parent, but they differ completely in when they appear, how they grow, how they change with age, and how they are treated [1][2].
Key points
- Port-wine stain is usually present at birth and persists
- Infantile hemangioma may be absent at birth, appears in the first weeks and grows quickly
- A port-wine stain is usually flat at first
- A hemangioma may be raised if superficial, or a bluish swelling if deep
- Port-wine stains do not fade on their own, while most hemangiomas shrink gradually over years
How to tell them apart
At birth, a port-wine stain is usually already visible, while a hemangioma may be absent or only a faint mark. In growth, a port-wine stain grows in proportion with the child, while a hemangioma grows rapidly during the first months.
In colour, a port-wine stain is pink, red or purple, while a hemangioma is bright red or bluish. In surface, a port-wine stain is usually flat and a hemangioma may be raised. Over time a port-wine stain persists and can darken and thicken, while a hemangioma gradually involutes.
In treatment, port-wine stains are treated with vascular laser, especially pulsed dye laser, while hemangiomas are observed or treated with oral propranolol when needed. In associations, port-wine stains in certain facial locations can be linked with Sturge-Weber syndrome, and large segmental facial hemangiomas can be linked with PHACE syndrome [1][5][6].
Port-wine stain
A port-wine stain, also called a capillary malformation, is a congenital change in the small blood vessels of the skin. It is typically present at birth, flat, pink to red or purple, well demarcated, and persistent [3].
As the child grows, the mark grows in proportion with the body. Over years it can become darker and thicker, and the surface may become rougher or cobblestoned.
When a port-wine stain needs further assessment
Particular attention is given to a port-wine stain on the forehead, upper eyelid or the ophthalmic (V1) distribution of the trigeminal nerve. These distributions can be associated with Sturge-Weber syndrome [5].
- Neurological problems or seizures
- Glaucoma and other eye complications
- Vascular changes in the membranes covering the brain
- A need for eye and neurological assessment depending on the site and size of the stain
Infantile hemangioma
An infantile hemangioma is a benign vascular tumour of childhood. It may not be obvious at birth, then appears and grows during the first weeks of life. It follows a pattern of appearance, rapid growth, plateau, then gradual involution [1][4].
Superficial hemangiomas are bright red, raised and soft or compressible. Deep hemangiomas appear bluish or skin coloured as a swelling under the skin and are less obvious. Both types can occur together in the same child.
When a hemangioma needs treatment
Most infantile hemangiomas need only observation. Early assessment matters for the higher risk group, and where treatment is needed, oral propranolol is the first line option in many suitable cases [1].
- Growing very rapidly
- Close to the eye with a risk to vision
- Around the nose or mouth
- Causing difficulty with feeding or breathing
- Ulcerated, painful or bleeding
- Very large or widespread
- Segmental or extensive on the face
What is PHACE syndrome
Large segmental facial hemangiomas can be associated with PHACE syndrome in some children [6].
- P posterior fossa brain malformations
- H hemangioma
- A arterial anomalies
- C cardiac defects
- E eye abnormalities
Do these marks disappear
Most infantile hemangiomas do involute after the growth phase, but involution takes several years and can leave fine telangiectasia, loose or redundant skin, fibrofatty tissue, or changes in skin colour and texture.
A port-wine stain usually does not fade. Untreated it persists for life and can darken and thicken with time. Pulsed dye laser is the most established treatment, lightening the mark over several sessions [3].
Not every red mark is a hemangioma
Many vascular skin marks look alike. Diagnosis rests on the timing of appearance, the shape, the texture, the site and the pattern of growth. These points let a dermatologist separate a port-wine stain from a hemangioma and from other vascular malformations [2].
When to see a dermatologist
Bring the child for assessment if there is a red mark present since birth, especially on the face, a red lesion that started enlarging quickly in the first weeks, a mark near the eye or on the eyelid, a large or multiple lesions, ulceration, bleeding or pain, or any problem with vision, breathing or feeding.
Early assessment matters because some vascular birthmarks need treatment during a narrow window to prevent complications.
Frequently asked questions
Is a port-wine stain dangerous?
It is usually benign, but the location matters. Marks on the forehead and upper eyelid may need further assessment to exclude an association with Sturge-Weber syndrome.
Is a hemangioma cancer?
No. An infantile hemangioma is benign and is not cancer.
Which one fades with time?
Infantile hemangioma usually involutes gradually, while a port-wine stain does not disappear on its own.
Does every hemangioma need propranolol?
No. Many small low risk hemangiomas need observation only. The doctor decides based on size, site, growth speed and possible complications.
Can laser treat a port-wine stain?
Yes. Pulsed dye laser is used in many cases and usually needs several sessions.
References and sources
- [1] Krowchuk DP, et al. American Academy of Pediatrics clinical practice guideline for the management of infantile hemangiomas. Pediatrics. 2019;143(1):e20183475.
- [2] International Society for the Study of Vascular Anomalies. ISSVA classification of vascular anomalies.
- [3] DermNet. Port-wine stain (capillary malformation).
- [4] DermNet. Infantile haemangioma.
- [5] DermNet. Sturge-Weber syndrome and capillary malformations.
- [6] DermNet. PHACE syndrome.
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