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首页> 外文期刊>Medicine. >Co-occurrence of TCF3-PBX1 gene fusion, and chromosomal aberration in a pediatric pre-B cell acute lymphoblastic leukemia with clitoris swelling
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Co-occurrence of TCF3-PBX1 gene fusion, and chromosomal aberration in a pediatric pre-B cell acute lymphoblastic leukemia with clitoris swelling

机译:TCF3-PBX1基因融合的共同发生,以及小儿前B预患中的染色体畸变,阴蒂肿胀肿瘤白血病

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RATIONALE:Clitoris swelling as the initial clinical presentation of acute lymphoblastic leukemia (ALL) is extremely rare. These patients may be misdiagnosed with acute myeloid leukemia or solid tumor, and the main treatment can also be delayed.PATIENT CONCERNS:A 2.10-year-old girl was referred to the pediatric surgery clinic with a worsening onset of clitoris swellings. The patient was afebrile and well appearing. Multiple retroperitoneal mass were confirmed by computed tomography (CT) and high serum neuron-specific enolase level was high. She was scheduled for an abdominal biopsy from the retroperitoneal mass suspicious of neuroblastoma.DIAGNOSES:The child was eventually diagnosed as having precursor B cell ALL with central nervous system involved, with TCF3-PBX1 fusion gene and additional chromosomal aberrations, based on examinations of the bone marrow and brain magnetic resonance imaging.INTERVENTIONS:Before the diagnosis of leukemia, the patient was given symptomatic treatment for 1?week. She was treated with chemotherapy in accordance with the Chinese Children's Cancer Group protocol 2015 after confirmed diagnosis.OUTCOMES:After induction chemotherapy for ALL, although the girl had transiently clinical remission, the bone marrow aspirate indicated a poor outcome. Our patient discontinued treatment and discharged. From literature review, there was only 1 case of in acute myeloid leukemia with clitoris swelling as the initial symptom.LESSONS:The clinical symptoms of ALL with clitoris swelling are not typical, with a high rate of misdiagnosis. When the cause of clitoris swelling is unknown, ALL should be considered. Bone marrow aspiration must be done before doing a more invasive investigation like biopsy.Copyright ? 2021 the Author(s). Published by Wolters Kluwer Health, Inc.
机译:理由:阴蒂肿胀作为急性淋巴细胞白血病(全部)的初始临床介绍性极为罕见。这些患者可能与急性髓性白血病或实体肿瘤误诊,主要治疗也可以延迟。值得关注的问题:一个2.10岁的女孩被提交给儿科手术诊所,阴蒂肿胀发病恶化。患者出现良好,出现良好。通过计算断层扫描(CT)和高血清神经元特异性烯醇酶水平证实了多种腹膜内肿块。她被安排从腹膜后瘤的腹部活组织检查,神经细胞瘤。诊断为具有涉及的中枢神经系统的患者诊断为具有中枢神经系统的前体B细胞,基于检查的检查骨髓和脑磁共振成像。Interventions:在白血病诊断之前,患者给予症状治疗1?周。在确认诊断后,她根据中国儿童癌症组议定书进行了化疗治疗。所有人:诱导化疗后,虽然女孩患有临床缓解,但骨髓抽吸表示较差的结果。我们的病人停止治疗和排放。从文献综述中,只有1例中急性髓性白血病,阴蒂肿胀作为初始症状,伴随着阴蒂肿胀的临床症状并不典型,误诊率高。当阴蒂肿胀的原因未知时,应该考虑所有。在进行更侵入性的研究之前,必须进行骨髓抱负,如活检。 2021提交人。由Wolters Kluwer Health,Inc。出版

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