Mode
Text Size
Log in / Sign up

Review of single-stage surgery for orbital and parasellar infantile hemangioma in a 55-day-old infantA Baby Had Two Rare Brain Tumors at Once — and Surgeons Removed Both

AI-generated summary of the cited source, checked by automated accuracy review. How we work

Key Takeaway
Consider surgical resection for solitary orbital/parasellar IH with diagnostic uncertainty and significant symptomatology, noting limited generalizability.

This publication is a case report detailing the management of a 55-day-old female infant presenting with orbital and intracranial infantile hemangioma. The intervention involved a single-stage left pterional approach designed for the simultaneous resection of both orbital and parasellar lesions. The setting and specific follow-up duration were not reported in the source text. The primary outcomes assessed included achieving a definitive histopathological diagnosis and providing relief of mass effect. Secondary outcomes focused on the resolution of proptosis, the status of neurological deficits, and the extent of lesion resection.

The main results indicated that histopathological examination confirmed the diagnosis of cellular infantile hemangioma. Following the procedure, the patient experienced complete resolution of proptosis and no neurological deficits. Additionally, total resection of the lesions was achieved. The safety profile was characterized by an uneventful recovery, with no adverse events, serious adverse events, or discontinuations reported. However, the sample size was one, which inherently limits the statistical power and generalizability of these specific outcomes.

The authors acknowledge a key limitation: the absence of a management consensus for solitary orbital and parasellar infantile hemangiomas without cutaneous manifestations. Consequently, while the practice relevance suggests that isolated intracranial or orbital infantile hemangioma should be included in the differential diagnosis of pediatric masses even without skin involvement, the evidence is restricted to this single case. Surgical resection may be considered a safe and effective primary strategy when facing diagnostic uncertainty and significant symptomatology, but clinicians should interpret these results with caution given the lack of broader comparative data.

When a baby's eye begins to push forward

In the first weeks of life, a baby's face should be growing, not changing shape in alarming ways. But at 55 days old, this infant girl's left eye began visibly bulging outward — a condition called proptosis — and it was getting worse week by week.

It was the kind of finding that stops parents and pediatricians alike. Something was pushing the eye from behind.

What the scans showed — and what they didn't

Magnetic resonance imaging (MRI) revealed two distinct masses: one wrapped around the optic nerve inside the left orbit (the bony socket of the eye), and a second mass near the parasellar region — an area deep at the base of the skull, near where critical blood vessels and nerves cluster around the pituitary gland.

The imaging characteristics were concerning. The tumors looked, on the scan, very much like a meningioma — a type of tumor that can behave aggressively, particularly when it encases a nerve.

But the infant had no skin lesions. No telltale red birthmarks that often accompany the most common type of these tumors. Nothing on the outside to hint at what might be happening within.

The diagnosis that changes everything

Infantile hemangiomas (IHs) are the most common benign (non-cancerous) tumors of infancy. Most are visible on the skin as raised, red, or strawberry-like patches. They grow in the first year of life and then slowly shrink on their own.

But occasionally, hemangiomas grow inside the body — behind the eye, inside the skull, along internal organs — without any visible skin involvement. When that happens, they can be nearly impossible to diagnose without tissue.

Having two simultaneous deep hemangiomas — one orbital, one intracranial — with no external signs is exceptionally rare. The medical literature contains very few documented cases.

When surgery is both the question and the answer

The medical team faced a difficult situation. The imaging couldn't definitively distinguish between a hemangioma and something more dangerous. The infant was showing symptoms — the eye was already being displaced, and the mass near the brain base posed risk to surrounding structures.

A multidisciplinary team made the decision to operate — removing both lesions in a single surgery using a pterional approach (an entry through the side of the skull near the temple). The goal was twofold: relieve the pressure on the optic nerve and nearby brain structures, and obtain tissue to finally know what they were dealing with.

This kind of complex surgical decision in a 55-day-old infant requires a highly specialized team at a center experienced in pediatric neurosurgery.

Histopathological examination — looking at the tissue under a microscope — confirmed the diagnosis of cellular infantile hemangioma. Positive staining for two markers, GLUT-1 and CD31, is characteristic of IH and helped distinguish it from other vascular tumors or malignancies.

The infant recovered without complications. The proptosis resolved completely. No neurological deficits were observed. Follow-up imaging confirmed that both tumors had been fully removed.

Why this case matters beyond one baby

Infantile hemangiomas without skin involvement are easy to miss — or to misdiagnose as something more dangerous. This case adds to a small but growing body of evidence that deep IHs should be included in the differential diagnosis (the list of possibilities doctors consider) for any infant presenting with orbital masses or unexplained intracranial lesions, even without characteristic skin findings.

For clinicians caring for infants with unusual imaging findings, this case reinforces that hemangioma should remain on the radar — and that surgery can be both diagnostic and curative when other methods fall short.

What this means for parents

If your infant or young child develops progressive eye bulging, decreased vision, unexplained neurological symptoms, or visible swelling around the eye, seek evaluation promptly. These symptoms are not always serious, but they warrant immediate assessment by a pediatrician and, if indicated, a specialist in pediatric ophthalmology or neurology.

For most infantile hemangiomas — particularly the common surface variety — surgery is not needed, and many respond well to medications like propranolol. Internal hemangiomas are different, and management must be individualized.

The limits of a single case report

A case report represents a sample size of one. It documents what happened in this particular infant but cannot guide general treatment decisions on its own. The approach taken here — single-stage surgical resection — was appropriate given the specific clinical situation, but it is not a template that applies to all similar presentations.

What comes next

The authors call for greater awareness among radiologists, neonatologists, and pediatric neurosurgeons that internal IHs can mimic other lesions on imaging. Broader awareness and more documented cases will help the field develop clearer diagnostic criteria and management guidelines for this rare presentation — so that future infants benefit from faster, more confident diagnosis and care.

Study Details

Study typeGuideline
EvidenceLevel 5
PublishedApr 2026
View Original Abstract ↓
BackgroundSolitary orbital and parasellar infantile hemangiomas (IHs) without cutaneous manifestations are exceptionally rare, posing significant diagnostic and therapeutic challenges due to the absence of management consensus.Case presentationA 55-day-old female infant presented with progressive left-sided proptosis over the course of one month. Preoperative magnetic resonance imaging (MRI) revealed homogeneously enhancing masses in the left orbit (encasing the optic nerve) and the parasellar region, in which imaging characteristics resembled those of a meningioma. No cutaneous lesions or features of PHACE syndrome were identified. Following multidisciplinary team consultation, a single-stage left pterional approach for the simultaneous resection of both the orbital and parasellar lesions, with the aim of establishing a definitive histopathological diagnosis and relieving mass effect. Histopathological examination confirmed the diagnosis of cellular IH, which could be supported by characteristic morphology and positive immunohistochemical staining for GLUT-1 and CD31. Postoperative recovery was uneventful, with complete resolution of proptosis and no neurological deficits. Imaging confirmed total resection of both lesions.ConclusionsThis case emphasizes that isolated intracranial/orbital IH should be included in the differential diagnosis of pediatric masses, even in the absence of skin involvement. When facing diagnostic uncertainty and significant symptomatology, surgical resection can be a safe and effective primary strategy, providing definitive diagnosis and immediate decompression.
Free Newsletter

Clinical research that matters. Delivered to your inbox.

Join thousands of clinicians and researchers. No spam, unsubscribe anytime.