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Acute myeloid leukemia presenting as a spontaneous hemotympanum: A Case Report and review of the literature

机译:急性髓性白血病呈现为自发血禁杂志:对文献的案例报告和审查

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ObjectiveTo present a unique cause of spontaneous unilateral hemotympanum.Case reportWe present the case of a 71-year-old male with known history of acute myeloid leukemia (AML) who presented for evaluation of one month of aural fullness. The patient denied worsening of baseline hearing, otorrhea, or tinnitus but did endorse brief episodic vertigo that resolved without intervention. He also denied history of head trauma. Physical exam revealed unilateral hemotympanum. There were no cranial nerve deficits. There was incidental note of an infectious appearing subdural collection on a CT temporal bone obtained for further evaluation of the hemotympanum. Therefore, the patient underwent combined mastoidectomy and temporal craniotomy. Cytopathology demonstrated leukemic infiltrates and no evidence of active infection.ConclusionsChloroma, extra-medullary deposition of leukemic cells, has rarely been reported in the temporal bone. We report a rare instance of temporal bone chloroma which presented as spontaneous hemotympanum. In the absence of an explanatory cause of hemotympanum, leukemic blast crisis resulting in chloroma can be considered.
机译:ObjectiveTo提出了一个独特的自发单侧血红蛋白的原因。Case报告我们展示了一个71岁男性的案件,其中包含了急性髓性白血病(AML)的已知历史,他们提出了一个月的听觉满志。患者拒绝恶化基线听力,耳聋或耳鸣,但确实是在没有干预的情况下解决的简要内容眩晕。他还否认了头部创伤的历史。体育考试显示单侧血幼对话。没有颅神经缺陷。在获得的CT颞骨上有传染性出现的闭塞性收集的偶然记录,以进一步评估血偶杂珠。因此,患者接受了联合乳腺切除术和颞枝肉瘤菌。缩影病理学证明白血病浸润,没有有活性感染的证据。颞骨很少报道同性全脑血液瘤细胞的超髓质沉积。我们举报了少颞骨氯瘤的罕见例,其呈现为自发血幼对比百年运动。在没有血液运动的解释性原因的情况下,可以考虑导致氯瘤的白血病爆炸危机。

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