一名 13 个月大的患有眼耳鼻畸形综合征的男婴体内的肝母细胞瘤

IF 0.9 4区 医学 Q4 HEMATOLOGY
Kriti Kumar, Chitra Prasad, Diana Masse, Jennifer Seelisch
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引用次数: 0

摘要

背景:眼-心-齿综合征(OFCD)是一种 X 连锁显性遗传病,通常在男性中致死:观察结果:一名 13 个月大的 OFCD 综合征男性患者出现肝母细胞瘤。他按照标准治疗方案接受了化疗,并进行了手术切除,并发症很少。他接受硫代硫酸钠治疗以保护耳部,并接受右雷佐生治疗以保护心脏。确诊五年后,他的病情仍在缓解中:恶性肿瘤在 OFCD 综合征患者中也有报道,但我们的患者是唯一一名患有肝母细胞瘤的 OFCD 综合征男性患者。鉴于这种疾病的罕见性,恶性肿瘤可能是疾病谱的一部分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hepatoblastoma in a 13-month-old Male With Oculofaciocardiodental Syndrome.

Background: Oculofaciocardiodental (OFCD) syndrome is an X-linked dominant condition that is typically lethal in males.

Observations: A 13-month-old male patient with OFCD syndrome presented with hepatoblastoma. He received chemotherapy per standard of care and had a surgical resection with few complications. He received sodium thiosulfate for otoprotection and dexrazoxane for cardioprotection. Five years after diagnosis, he remains well and in remission.

Conclusions: Malignancies have been reported in patients with OFCD syndrome; however, our patient is the only male with OFCD syndrome described with hepatoblastoma. Given the rarity of this condition, malignancy may be part of the spectrum of disease.

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来源期刊
CiteScore
1.90
自引率
8.30%
发文量
415
审稿时长
2.5 months
期刊介绍: ​Journal of Pediatric Hematology/Oncology (JPHO) reports on major advances in the diagnosis and treatment of cancer and blood diseases in children. The journal publishes original research, commentaries, historical insights, and clinical and laboratory observations.
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