Evidence map›Paper›PMID 40794370›Full record

ArticleJournal of ultrasound2025

Not only vascular lesions: a case report of infantile fibrosarcoma.

L Marone, A Masucci, F Barbato, F Ausiello, R Zeccolini, M E Errico, F Esposito

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Article in Journal of ultrasound, 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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5 · Who and what money

Authors and funding

7 authors.

L MaroneRadiology Department, University "Luigi Vanvitelli", Naples, Italy. lauramarone95@outlook.it.ORCID http://orcid.org/0009-0001-3141-1967
A MasucciRadiology Department, University "Federico II", Naples, Italy.
F BarbatoDermatology Department, Santobono-Pausilipon Children Hospital, Naples, Italy.
F AusielloDermatology Department, Santobono-Pausilipon Children Hospital, Naples, Italy.
R ZeccoliniRadiology Department, University "Luigi Vanvitelli", Naples, Italy.
M E ErricoPathology Department, Santobono-Pausilipon Children Hospital, Naples, Italy.
F EspositoEmergency Radiology Department, Santobono-Pausilipon Children Hospital, Naples, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo present a rare case of congenital infantile fibrosarcoma (IFS) mimicking a vascular anomaly and to emphasize the diagnostic value of color Doppler and contrast-enhanced ultrasound (CEUS) in differentiating IFS from benign vascular tumors such as congenital hemangioma. MATERIALS AND

methodsWe present the case of a 4-month-old male with a congenital lumbosacral mass initially suggestive of congenital hemangioma. Ultrasound and Doppler examination demonstrated a highly vascularized lesion; however, the imaging findings remained equivocal for a definitive diagnosis of hemangioma. MRI confirmed a solid, hypervascular lesion without spinal involvement. Histopathology identified a spindle cell neoplasm consistent with IFS, likely driven by an NTRK rearrangement. The mass was surgically excised with a good postoperative recovery.

resultsDoppler and CEUS findings showed vascular features atypical for congenital hemangiomas, which generally present with diffuse, centripetal enhancement and sustained contrast uptake. In contrast, this lesion exhibited an organized radial vascular pattern with early unidirectional enhancement and rapid washout. However, imaging findings remained equivocal for a definitive diagnosis of hemangioma, necessitating further histopathological evaluation, leading to timely surgical management.

conclusionsThis case underscores the diagnostic challenge in distinguishing IFS from benign vascular tumors and highlights the importance of histological evaluation. Early recognition is essential, as IFS, though locally aggressive, has a favorable prognosis when promptly and properly managed.

Indexed as

CEUSDopplerHemangiomaInfantile fibrosarcomaUltrasoundVascular malformations

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.