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Meningococcal purpura fulminans and severe myocarditis with clinical meningitis but no meningeal inflammation: a case report

机译:脑膜炎双球菌性紫癜和重度心肌炎合并临床性脑膜炎但无脑膜炎症:一例报告

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During fulminant meningococcal septicaemia, meningococci are often observed in the cerebrospinal fluid (CSF) although the patients have frequently no meningeal symptoms. Meningococcal meningitis, by contrast, usually features clinical meningeal signs and biochemical markers of inflammation with elevated white blood cell count (pleiocytosis) in the CSF. Cases of typical symptomatic meningitis without these biochemical features are uncommon in adults. A 21-year-old male presented with meningococcal purpura fulminans and disseminated intravascular coagulation (DIC) associated with multiple organ dysfunction syndrome requiring hospitalization in the Intensive Care Unit. Despite typical meningeal clinical signs, lumbar puncture showed no pleiocytosis, normal glycorachia and normal proteinorachia, whereas the lactate concentration in the CSF was high (5.8?mmol/L). CSF culture showed a high inoculum of serogroup C meningococci. On day 2, after initial improvement, a recurrence of hypotension led to the diagnosis of acute meningococcal myocarditis, which evolved favourably within a week. During the hospitalization, distal ischemic and necrotic lesions were observed, predominantly on the fingertips, which were treated with local and systemic vasodilators. We report a rare case of adult meningococcal disease characterized by an intermediate form of meningitis between purulent meningitis and meningeal inoculation from fulminant meningococcal septicaemia, without classical signs of biological inflammation. It highlights the diagnostic value of CSF lactate, which may warrant administration of a meningeal dosing regimen of beta-lactam antibiotics. This case also demonstrates the potential severity of meningococcal myocarditis; we discuss its pathophysiology, which is distinct from other sepsis-related cardiomyopathies. Finally, the observed effects of vasodilators on the meningococcal skin ischemia in this case encourages future studies to assess their efficacy in DIC-associated necrosis.
机译:在暴发性脑膜炎球菌败血症期间,尽管患者通常没有脑膜症状,但经常在脑脊液(CSF)中观察到脑膜炎球菌。相比之下,脑膜炎球菌性脑膜炎通常表现为脑膜炎体征和炎症的生化标志物,脑脊液中白细胞计数升高(胞吞)。没有这些生化特征的典型症状性脑膜炎在成年人中并不常见。一名21岁的男性患者出现脑膜炎球菌性紫癜,并伴有多器官功能障碍综合征的弥散性血管内凝血(DIC),需要在加护病房住院治疗。尽管有典型的脑膜临床征象,但腰穿未显示出多卵细胞增多症,正常糖尿和正常蛋白尿症,而脑脊液中的乳酸浓度很高(5.8?mmol / L)。脑脊液培养物显示出C群脑膜炎球菌的高接种量。最初改善后的第2天,低血压的复发导致了急性脑膜炎球菌性心肌炎的诊断,并在一周之内进展顺利。在住院期间,观察到远端缺血性和坏死性病变,主要在指尖,用局部和全身性血管扩张药治疗。我们报告了罕见的成人脑膜炎球菌疾病病例,其特征是化脓性脑膜炎和暴发性脑膜炎球菌败血症引起的脑膜炎接种之间存在中间形式的脑膜炎,而没有经典的生物学炎症迹象。它强调了脑脊液乳酸的诊断价值,这可能需要使用β-内酰胺类抗生素的脑膜给药方案。该病例还证明了脑膜炎球菌性心肌炎的潜在严重性。我们讨论其病理生理学,与其他败血症相关的心肌病不同。最后,在这种情况下观察到的血管扩张剂对脑膜炎球菌皮肤缺血的影响,鼓励了进一步的研究,以评估其在DIC相关性坏死中的功效。

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