Evidence map›Paper›PMID 41170443›Full record

ArticleFrontiers in ophthalmology2025

Case Report: Mature congenital teratoma masquerading as orbital cellulitis in a 12-day-old infant.

Alyssa C Huelsbeck, Colin P Froines, Suzanne W van Landingham

Abstract readCase Reports
In one paragraph

Article in Frontiers in ophthalmology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Alyssa C HuelsbeckSchool of Medicine and Public Health, University of Wisconsin, Madison, WI, United States.
Colin P FroinesDepartment of Ophthalmology and Visual Sciences, University of Wisconsin, Madison, WI, United States.
Suzanne W van LandinghamDepartment of Ophthalmology and Visual Sciences, University of Wisconsin, Madison, WI, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Congenital orbital teratoma is a rare neoplasm that typically presents as progressive, unilateral proptosis in an otherwise healthy newborn. Management includes prompt surgical excision, with guarded visual prognosis but excellent survival. Case presentation: A 12-day-old healthy infant presented with progressive left eye swelling and proptosis. She was initially diagnosed with orbital cellulitis and treated with IV antibiotics. Magnetic resonance imaging (MRI) showed a 1.5x1.9x2.1 cm left intraconal mass with 9mm of proptosis and significant mass effect. The patient underwent left lateral orbitotomy for biopsy and excision of the mass. Histopathologic examination showed neutrophilic inflammation and granulation tissue with foci of gastrointestinal epithelium, cartilage, squamous epithelium, and ganglion cells, consistent with mature congenital teratoma. The postoperative course was uncomplicated and there is no sign of recurrence at 21 months of age. Conclusion: Orbital teratoma should be suspected in a rapidly growing orbital mass in a newborn. Imaging showing characteristic findings should lead to prompt excisional biopsy. Tumor markers can be used to monitor for recurrence, which is rare.

Indexed as

case reportcongenital teratomaneonatal orbital massorbital cellulitisorbitotomyproptosis

Identifiers

PMID41170443
PMCPMC12569518

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