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弥漫性脑转移性癌的罕见病例:一例报告。

Rare incidence of a diffuse brain metastatic carcinoma: A case report.

作者信息

Sun Xiang, Chen Zhijuan, Yang Weidong, Yu Fuhua, Zhao Jingwang, He Ping, Wang Zengguang

机构信息

Department of Neurosurgery, Tianjin Medical University General Hospital, Tianjin 300052, P.R. China.

出版信息

Oncol Lett. 2014 Oct;8(4):1807-1809. doi: 10.3892/ol.2014.2377. Epub 2014 Jul 24.

Abstract

Brain metastases generally present in the parenchyma of the brain. In the current report, a very rare case of brain metastasis, which simultaneously invaded the subgaleal region, the skull, and the dural and cavernous sinuses is presented. The patient, a 54-year-old female, complained of a progressive headache and exhibited the symptoms of intracranial hypertension. Coronal contrast-enhanced T1-weighted magnetic resonance imaging (MRI) showed high intensity signals in the subgaleal tissue of the left frontoparietal area, as well as in the dural and the cavernous sinuses. The patient was initially diagnosed with an intracranial infection, however, the administered treatment was ineffective. The patient subsequently underwent a biopsy and the pathological diagnosis was determined as a metastatic adenocarcinoma; a primary tumor was not identified during the examinations. Surgical removal of certain metastases and a decompressive craniectomy were performed to relieve the intracranial hypertension. However, the prognosis was unsatisfactory. The patient's neurological condition progressively worsened and an axial computed tomography scan with a bone window demonstrated a bulging growth in the brain tissue. The patient succumbed after one month due to the widespread metastasis. Thus, this case presents the unusual clinical development of this type of metastatic adenocarcinoma. In addition, due to the intracranial hypertension, the unusual sites of the high intensity signals in the MRI and the lack of a primary tumor, the patient was misdiagnosed with an intracranial infection. Furthermore, this case highlights the necessity for conducting a biopsy as soon as possible and demonstrates the poor prognosis associated with this type of patient.

摘要

脑转移瘤通常出现在脑实质内。在本报告中,呈现了一例非常罕见的脑转移瘤病例,该病例同时侵犯了帽状腱膜下区域、颅骨、硬脑膜和海绵窦。患者为一名54岁女性,主诉进行性头痛并出现颅内高压症状。冠状位对比增强T1加权磁共振成像(MRI)显示左额顶叶区域帽状腱膜下组织以及硬脑膜和海绵窦内有高信号。患者最初被诊断为颅内感染,然而,所给予的治疗无效。患者随后接受了活检,病理诊断为转移性腺癌;检查期间未发现原发性肿瘤。进行了部分转移瘤的手术切除和减压颅骨切除术以缓解颅内高压。然而,预后并不理想。患者的神经状况逐渐恶化,轴向计算机断层扫描的骨窗显示脑组织有突出性生长。患者在一个月后因广泛转移而死亡。因此,该病例呈现了这种类型转移性腺癌不寻常的临床发展过程。此外,由于颅内高压、MRI中高信号的不寻常部位以及缺乏原发性肿瘤,患者被误诊为颅内感染。此外,该病例强调了尽早进行活检的必要性,并证明了这类患者预后较差。

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