Parney I F, Johnson E S, Allen P B
Department of Surgery, University of Alberta, Edmonton, Canada.
Neurosurgery. 1997 Oct;41(4):965-71. doi: 10.1097/00006123-199710000-00041.
We present a case similar to previously described cases of idiopathic hypertrophic cranial pachymeningitis. However, our patient responded to antituberculous therapy. This raises the possibility that some cases of "idiopathic" hypertrophic cranial pachymeningitis may represent occult tuberculous disease.
A 55-year-old woman presented with a right fourth nerve palsy and a 5-month history of headaches. Magnetic resonance imaging with gadolinium revealed thick enhancing dura on the right half of the tentorium cerebelli, with edema of the adjacent midbrain, pons, and cerebral peduncle.
Open biopsy of the tentorial lesion revealed only dense fibrosis with histiocytic infiltration. An exhaustive search failed to demonstrate an underlying cause. In particular, mycobacterial stains/cultures were negative, there was no granuloma formation, and the chest x-ray was unremarkable. However, because of a strongly positive purified protein-derivative skin test and residence in an area endemic for tuberculosis, the patient was placed on antituberculous medications.
The patient's symptoms and signs resolved with antituberculous therapy. Resolution of the tentorial lesion was confirmed by gadolinium-enhanced magnetic resonance imaging. We conclude that this case represented occult tuberculous disease. An empiric trial of antituberculous therapy may be warranted in other cases of apparently idiopathic hypertrophic cranial pachymeningitis.
我们报告一例与先前描述的特发性肥厚性硬脑膜炎病例相似的病例。然而,我们的患者对抗结核治疗有反应。这增加了一些“特发性”肥厚性硬脑膜炎病例可能代表隐匿性结核疾病的可能性。
一名55岁女性,出现右侧动眼神经麻痹及5个月的头痛病史。钆增强磁共振成像显示小脑幕右侧硬膜增厚强化,相邻中脑、脑桥及大脑脚水肿。
小脑幕病变的开放活检仅显示致密纤维化伴组织细胞浸润。全面检查未能发现潜在病因。特别是,分枝杆菌染色/培养结果为阴性,无肉芽肿形成,胸部X线检查无异常。然而,由于纯化蛋白衍生物皮肤试验强阳性且居住在结核病流行地区,该患者接受了抗结核药物治疗。
患者的症状和体征通过抗结核治疗得以缓解。钆增强磁共振成像证实小脑幕病变消退。我们得出结论,该病例代表隐匿性结核疾病。对于其他明显特发性肥厚性硬脑膜炎病例,抗结核治疗的经验性试验可能是必要的。