Hemangioma (Infantile) ICD-10: D18.01
Often searched as: red birthmark baby, raised red lump on baby skin, strawberry mark on baby, growing red bump on baby, red skin growth in infant, hemangioma photos, hemangioma treatment, infantile hemangioma…
Clinical urgency level
Systems Affected
Severity Levels
mild
Small, uncomplicated hemangioma on the trunk or limb, not near critical structures, involuting normally — observation only.
moderate
Hemangioma near the eye, nose, lips, or ear with risk of functional impairment; or ulcerating hemangioma causing pain and wound care challenges — requires medical treatment (propranolol).
severe
Large segmental hemangioma on the face (PHACE syndrome — heart, brain, eye anomalies), airway hemangioma (stridor, breathing difficulty), liver hemangiomatosis (heart failure risk), or multiple cutaneous hemangiomas (>5 — screen for internal hemangiomas) — urgent specialist evaluation required.
Red Flags
- Hemangioma near or over the eye (risk of amblyopia / permanent vision loss if untreated)
- Hemangioma on the nose, lips, or ear causing distortion or feeding problems
- Stridor (noisy breathing) in an infant with a facial hemangioma — possible airway involvement
- Ulceration with significant pain, bleeding, or signs of infection
- More than 5 small hemangiomas on the skin — screen for liver or internal hemangiomas
- Large hemangioma on the face (>5cm) with segmental distribution — possible PHACE syndrome workup needed
Clinical Presentation
Infantile hemangioma — bright red strawberry mark on the cheek of an infant
Source: Wikimedia Commons (CC BY-SA 3.0 )
Hemangioma image gallery — DermNet NZ
View gallery on DermNet NZ (image gallery reference)When to See a Doctor
See a pediatrician or pediatric dermatologist if your baby's hemangioma is near the eye, on the nose or lips, ulcerating, or growing rapidly. Hemangiomas near critical structures need early treatment with propranolol (oral) to prevent permanent complications. Most hemangiomas on the trunk or limbs away from critical areas can be monitored.
Differential Diagnosis
- Port wine stain (vascular malformation — present at birth, doesn't grow or involute)
- Pyogenic granuloma (fast-growing, bleeds easily — usually in older children)
- Venous malformation (soft, compressible, bluish — present at birth)
- Kaposiform hemangioendothelioma (KHE — rare, aggressive, can cause thrombocytopenia)
- Tufted angioma
- Naevus flammeus (salmon patch / stork bite — fades in first year)
Comorbidities
- PHACE syndrome (large facial hemangioma + posterior fossa brain anomalies + arterial/cardiac/eye anomalies)
- LUMBAR syndrome (lumbosacral hemangioma + spinal anomalies)
- Liver hemangiomatosis (multiple liver lesions — hypothyroidism and heart failure risk)
- Ulceration (most common complication — painful, infection-prone)
Prognosis
The vast majority of infantile hemangiomas follow a predictable course: rapid growth in the first 3–6 months of life, plateau, then slow involution beginning around age 1. By age 5, ~50% have involuted; by age 10, ~90%. However, residual fibrofatty tissue or skin changes may remain after involution. Propranolol (oral) is the first-line treatment for complicated or high-risk hemangiomas, achieving dramatic results when started early (first weeks to months of life). Timely treatment prevents the irreversible complications — amblyopia, airway compromise, permanent disfigurement.
Detailed Overview
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