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首页> 外文期刊>Journal of pediatric endocrinology & metabolism: JPEM >Hepatoblastoma presenting as precocious puberty: a case report
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Hepatoblastoma presenting as precocious puberty: a case report

机译:表现为性早熟的肝母细胞瘤:一例报告

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摘要

Hepatoblastoma (HB), a primary liver tumor in childhood, is often accompanied by alpha-fetoprotein (AFP) secretion, and sometimes by beta-human chorionic gonadotropin hormone (beta-hCG) secretion, and this can cause peripheral precocious puberty (PPP). We describe a case of PPP associated with HB. Laboratory tests showed an increase in AFP, beta-hCG and testosterone values, and suppression of follicle-stimulating hormone and luteinizing hormone levels. After chemotherapy and surgery, AFP, beta-hCG and testosterone levels normalized and signs of virilization did not progress further. The child did not show evidence for tumor recurrence after 16 months of follow-up. New therapeutic approaches and early diagnosis may ensure a better prognosis of virilizing HB, than reported in the past. Assessment of PPP should always take into account the possibility of a tumoral source.
机译:肝母细胞瘤(HB)是儿童期的原发性肝肿瘤,通常伴有甲胎蛋白(AFP)分泌,有时还伴有β-人绒毛膜促性腺激素(β-hCG)分泌,这可导致周围性早熟(PPP) 。我们描述了与HB相关的PPP案例。实验室测试显示AFP,β-hCG和睾丸激素值增加,并抑制了促卵泡激素和促黄体生成素的水平。化疗和手术后,AFP,β-hCG和睾丸激素水平恢复正常,病毒化症状没有进一步发展。随访16个月后,该儿童未显示肿瘤复发的证据。与过去报道的情况相比,新的治疗方法和早期诊断可确保病毒性HB的预后更好。 PPP评估应始终考虑肿瘤来源的可能性。

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