免疫功能正常患者多发颅内结核瘤:一种罕见的中枢神经系统结核(CNS TB)原发性表现

None Muhammad Sohail Ajmal Ghoauri, None Fatima Abbas, None Nauman Ismat Butt, None Muhammad Bilal Rasheed, None Abdul Samad, None Farah Naz
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引用次数: 0

摘要

在包括巴基斯坦在内的大多数发展中国家,结核病是一个严重但有可能治愈的健康问题。我们报告的情况下,免疫功能正常的病人有多个颅内结核瘤没有脑膜炎的证据,这是一个罕见的表现中枢神经系统结核。男性,50岁,出现5次强直-阵挛性全身痉挛1天,右侧体无力2周,全身性头痛和间歇性低烧1个月。无肺结核接触史或既往病史报告。神经学检查显示,右上肢和右下肢均有张力增高,深肌腱反射过度,3/5的力量,并伴有右足底伸肌反应。脑部CT示左侧额叶及颞叶高密度区,周围血管源性水肿。ESR以86 mm/h升高。CSF分析显示drbc 0细胞/uL, WBC 783细胞/uL, 100%淋巴细胞,葡萄糖39 mg/dl,蛋白81 mg/dl, afb和Giemsa染色阴性。然而,CSF对GeneXpert-PCR-MTB呈阳性,但未检测到利福平耐药。脑MRI显示双侧大脑半球、丘脑、左侧基底节区、延髓和小脑多发弥散性边缘强化病变,伴病灶周围水肿,无脑膜强化。免疫抑制检查正常。诊断为多发性颅内结核瘤,并开始抗结核治疗。患者无症状,服用ATT依从性好,随访6周无不良反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multiple Intracranial Tuberculomas In Immunocompetent Patient: An Uncommon Primary Manifestation Of Central Nervous System Tuberculosis (CNS TB)
Tuberculosis (TB) is a serious yet potentially-curable health issue among most developing countries including Pakistan. We report the case of an immunocompetent patient having multiple intracranial tuberculomas without evidence of meningitis which is an uncommon manifestation of CNS tuberculosis. A 50-year old man presented with 5 episodes of tonic-clonic generalized fits for 1 day, right sided body weakness for 2 weeks, generalized headaches and intermittent low-grade fever for 1 month. No contact or past history of tuberculosis was reported. On neurologic examination, there was hypertonia, exaggerated deep tendon reflexes and power of 3/5 in both right upper limb and right lower limb with a right plantar extensor response. CT scan (Brain) showed hyperdense areas in left frontal and temporal lobes with surrounding vasogenic edema. ESR was raised at 86 mm/hour. CSF analysis demonstratedRBC 0 cells/uL, WBC 783 cells/uL with 100% lymphocytes, Glucose 39 mg/dl andProtein 81 mg/dl with negative organism microscopy onAFB and Giemsa staining. However, CSF was positive for GeneXpert-PCR-MTB but drug resistance was not detected to rifampicin. Brain MRI with FLAIR demonstrated multiple disseminated, rim enhancing lesions with perilesional edema in bilateral cerebral hemispheres, thalami, left basal ganglia, medulla oblangata and cerebellum having no meningeal enhancement. Workup for immune-suppression was normal. A diagnosis of multiple intracranial tuberculomas was established and Anti-tubercular therapy was commenced. He was asymptomatic and taking ATT with good compliance having no adverse affects by 6-week follow up.
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