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- W4293511005 abstract "Objective: We reviewed our experience with congenital hepatic hemangiomas (CHH) to assess the effectiveness of our treatment strategies. Methods: Clinical and pathologic features of children with CHH were reviewed. Results: Twenty-two cases of CHH were collected, 17 were resected and 5 were followed until resolution. In 17 with alpha-feto-protein (AFP) levels, 9 were elevated with 5 decreasing to normal before surgery. In six with tumors under 3 cm, five regressed between 1 and 13 months, one required removal 5 years after initial diagnosis. Postoperative histopathology of 17 cases showed abnormal vascular hyperplasia without lobular architecture. CD34 was expressed in all tumors, glucose transporter 1(Glut1) was negative. Conclusion: If the tumor is less than 3 cm, AFP is normal and there are no obvious complications, the lesion can be followed with regular assessment imaging. Surgical resection is an option in tumors less than 3 cm which have not regressed over time." @default.
- W4293511005 created "2022-08-30" @default.
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- W4293511005 date "2022-08-28" @default.
- W4293511005 modified "2023-10-17" @default.
- W4293511005 title "Clinical and Pathological Features of Congenital Hepatic Hemangioma in Children: A Retrospective Analysis" @default.
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- W4293511005 doi "https://doi.org/10.1080/15513815.2022.2114300" @default.
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