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小儿颅骨结核:一个不容忽视的诊断。

Calvarial tuberculosis in a paediatric patient: a diagnosis not to forget.

机构信息

Radiology Department, Instituto Português de Oncologia de Lisboa Francisco Gentil, Lisboa, Portugal.

Pathology Department, Instituto Português de Oncologia de Lisboa, Lisboa, Portugal.

出版信息

BMJ Case Rep. 2021 Nov 9;14(11):e244494. doi: 10.1136/bcr-2021-244494.

Abstract

We report the case of a 10-year-old boy that presented with a palpable, painless, frontal lesion. Laboratory assessments were unremarkable and the patient was asymptomatic. Initial investigation, with a skull radiograph and unenhanced CT scan, showed a lytic midline frontal lesion involving the inner and outer tables of the skull and a large subgaleal hypodense component. MRI further depicted communication with the epidural space and contact with the superior sagittal sinus (SSS). Subsequent evaluation by Doppler ultrasound and MR angiography excluded a sinus pericranii and showed normal patency of the SSS. Surgical biopsy revealed chronic granulomatous inflammation; PCR was positive for sp. One year after surgical resection and antitubercular therapy, there are no signs of recurrence. Primary calvarial involvement by tuberculosis is rare, even in developing countries. Familiarity with the expected clinical and imaging features is required to avoid diagnostic delay.

摘要

我们报告了一例 10 岁男孩的病例,其表现为可触及的、无痛的额部病变。实验室检查无明显异常,患者无症状。初步检查包括颅骨平片和增强 CT 扫描,显示溶骨性中线额部病变累及颅骨内、外板和较大的皮下低密度成分。MRI 进一步显示与硬脑膜外腔相通,并与上矢状窦(SSS)接触。随后通过多普勒超声和磁共振血管造影检查排除了窦颅皮,并显示 SSS 通畅。手术活检显示慢性肉芽肿性炎症;PCR 对 sp. 呈阳性。手术切除和抗结核治疗一年后,无复发迹象。即使在发展中国家,颅骨原发性结核也很少见。需要熟悉预期的临床和影像学特征,以避免诊断延误。

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