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一名从携带致病基因的母亲那里遗传了RB1基因缺失的双侧视网膜母细胞瘤患者:病例报告。

Trilateral retinoblastoma with an RB1 deletion inherited from a carrier mother: a case report.

作者信息

Amare P, Jose J, Chitalkar P, Kurkure P, Pai S, Nair C, Advani S

机构信息

Department of Medical Oncology, Tata Memorial Hospital, Parel, Bombay, India.

出版信息

Cancer Genet Cytogenet. 1999 May;111(1):28-31. doi: 10.1016/s0165-4608(98)00220-9.

Abstract

A presentation of intracranial tumor in bilateral and unilateral retinoblastoma with or without family history is termed as trilateral retinoblastoma (TRB). It always occurs either as a pineal tumor or supra/parasellar tumor, which differ in presentation and prognosis. We report here the first case of TRB with transmission of retinoblastoma gene (RB1) deletion from an unaffected mother (a carrier), presenting as concurrent intracranial neoplasm with bilateral retinoblastoma. The presence of RB1 mutation in both child and mother could be responsible for development of intracranial neoplasm which occurred simultaneously with bilateral RB in our patient. Our patient, who had a suprasellar mass, received radiation and intrathecal chemotherapy, and died 6 months after diagnosis. The occurrence of intracranial tumor in an asymptomatic stage can be avoided by routine computed tomography (CT) and magnetic resonance imaging (MRI) scan, and improved survival can be achieved by aggressive multimodality therapy.

摘要

双侧和单侧视网膜母细胞瘤伴或不伴有家族史时出现颅内肿瘤,被称为三边性视网膜母细胞瘤(TRB)。它总是表现为松果体肿瘤或鞍上/鞍旁肿瘤,其表现和预后有所不同。我们在此报告首例TRB病例,视网膜母细胞瘤基因(RB1)缺失从未受影响的母亲(携带者)传递给患儿,表现为双侧视网膜母细胞瘤并发颅内肿瘤。患儿和母亲均存在RB1突变,可能是导致颅内肿瘤发生的原因,该肿瘤在我们的患者中与双侧视网膜母细胞瘤同时出现。我们的患者有鞍上肿块,接受了放疗和鞘内化疗,诊断后6个月死亡。通过常规计算机断层扫描(CT)和磁共振成像(MRI)扫描可避免颅内肿瘤在无症状阶段出现,积极的多模式治疗可提高生存率。

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