L Marone, A Masucci, F Barbato, F Ausiello, R Zeccolini, M E Errico, F Esposito
{"title":"不只是血管病变:婴儿纤维肉瘤1例报告。","authors":"L Marone, A Masucci, F Barbato, F Ausiello, R Zeccolini, M E Errico, F Esposito","doi":"10.1007/s40477-025-01063-2","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>To 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.</p><p><strong>Materials and methods: </strong>We 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.</p><p><strong>Results: </strong>Doppler 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.</p><p><strong>Conclusions: </strong>This 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.</p>","PeriodicalId":51528,"journal":{"name":"Journal of Ultrasound","volume":" ","pages":""},"PeriodicalIF":1.4000,"publicationDate":"2025-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Not only vascular lesions: a case report of infantile fibrosarcoma.\",\"authors\":\"L Marone, A Masucci, F Barbato, F Ausiello, R Zeccolini, M E Errico, F Esposito\",\"doi\":\"10.1007/s40477-025-01063-2\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objectives: </strong>To 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.</p><p><strong>Materials and methods: </strong>We 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.</p><p><strong>Results: </strong>Doppler 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.</p><p><strong>Conclusions: </strong>This 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.</p>\",\"PeriodicalId\":51528,\"journal\":{\"name\":\"Journal of Ultrasound\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":1.4000,\"publicationDate\":\"2025-08-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Ultrasound\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1007/s40477-025-01063-2\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Ultrasound","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/s40477-025-01063-2","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING","Score":null,"Total":0}
Not only vascular lesions: a case report of infantile fibrosarcoma.
Objectives: To 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 methods: We 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.
Results: Doppler 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.
Conclusions: This 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.
期刊介绍:
The Journal of Ultrasound is the official journal of the Italian Society for Ultrasound in Medicine and Biology (SIUMB). The journal publishes original contributions (research and review articles, case reports, technical reports and letters to the editor) on significant advances in clinical diagnostic, interventional and therapeutic applications, clinical techniques, the physics, engineering and technology of ultrasound in medicine and biology, and in cross-sectional diagnostic imaging. The official language of Journal of Ultrasound is English.