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[勒米尔氏综合征:扁桃体炎后败血症合并脑膜炎及血管内消耗性凝血病,为传染性单核细胞增多症合并全鼻窦炎的并发症]

[Lemierre's post-tonsillitis sepsis with meningitis and intravascular consumption coagulopathy as complication of infectious mononucleosis with pansinusitis].

作者信息

Busch N, Mertens P R, Schönfelder T, Nguyen H, Marschall H U, Kierdorf H, Haase G, Urhahn R, Sieberth H G, Matern S

机构信息

Medizinische Kliniken II und III, Institut für Medizinische Mikrobiologie und Klinik für Radiologische Diagnostik, Klinikum der Technischen Hochschule Aachen.

出版信息

Dtsch Med Wochenschr. 1996 Jan 26;121(4):94-8. doi: 10.1055/s-2008-1042978.

DOI:10.1055/s-2008-1042978
PMID:8631245
Abstract

HISTORY AND CLINICAL FINDINGS

24 days after the onset of infectious mononucleosis, clinically and serologically confirmed, an otherwise healthy 18-year-old schoolboy developed a fulminant septicaemia with acute meningitis and loss of consciousness, consumptive coagulopathy and acute renal failure.

INVESTIGATIONS

Computed tomography demonstrated pansinusitis. Lumbar puncture produced purulent cerebrospinal fluid with 11,500 cells/microliters, predominantly granulocytes, protein 205 mg/dl, glucose 19 mg/dl, indicating bacterial meningitis. The suspected diagnosis of posttonsillitis septicaemia (Lemierre's syndrome) was confirmed by repeated demonstration of fusiform gram-negative bacteria in anaerobic blood cultures, identified as Fusobacterium necrophorum. Anaerobic CSF culture grew Prevotella bivia of the Bacteroidaceae family.

TREATMENT AND COURSE

Both the consumptive coagulopathy and the renal failure were successfully treated and the patient's condition stabilized. The sinuses were surgically drained under high doses of piperacillin/sulbactam and chloramphenicol. Despite the sensitivity of the cultured bacteria to the administered antibiotics the septic temperature continued, but disappeared within 4 days of metronidazole having been added. After 5 weeks of antibiotic treatment, three of them in an intensive care unit, the patient was discharged in good general condition.

CONCLUSION

This case illustrates that severe septicaemia caused by rare bacteria may follow an attack of infectious mononucleosis which had taken an uncomplicated course.

摘要

病史及临床检查结果

一名18岁原本健康的男学生,在传染性单核细胞增多症发病24天后,经临床及血清学确诊,出现暴发性败血症,伴有急性脑膜炎和意识丧失、消耗性凝血病及急性肾衰竭。

检查

计算机断层扫描显示全鼻窦炎。腰椎穿刺抽出脓性脑脊液,每微升含11,500个细胞,以粒细胞为主,蛋白205毫克/分升,葡萄糖19毫克/分升,提示细菌性脑膜炎。通过厌氧血培养反复检出梭形革兰氏阴性菌,确诊为扁桃体炎后败血症(勒米尔综合征),鉴定为坏死梭杆菌。厌氧脑脊液培养出拟杆菌科的二路普雷沃菌。

治疗及病程

消耗性凝血病和肾衰竭均得到成功治疗,患者病情稳定。在大剂量哌拉西林/舒巴坦和氯霉素治疗下,鼻窦进行了外科引流。尽管培养出的细菌对所用抗生素敏感,但败血症体温仍持续存在,不过在加用甲硝唑4天内体温消退。经过5周抗生素治疗,其中3周在重症监护病房,患者出院时一般状况良好。

结论

该病例表明,罕见细菌引起的严重败血症可能发生在病程无并发症的传染性单核细胞增多症发作之后。

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