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弓形虫脑炎患者对常规治疗不耐受,对复方磺胺甲噁唑脱敏。

Desensitization to trimethoprim-sulfamethoxazole in a toxoplasmic encephalitis patient who was intolerant to conventional treatments.

机构信息

Division of Infectious Diseases, Yokohama Municipal Citizen's Hospital, Japan.

Division of Infectious Diseases, Yokohama Municipal Citizen's Hospital, Japan.

出版信息

J Infect Chemother. 2020 Mar;26(3):289-293. doi: 10.1016/j.jiac.2019.10.008. Epub 2019 Nov 8.

Abstract

Toxoplasma gondii is an obligate intracellular protozoan that causes toxoplasmic encephalitis (TE) in immunocompromised patients. We describe a case of a 29-year-old Japanese man presenting with headache and vomiting. He had previously been diagnosed with human immunodeficiency virus infection. Magnetic resonance imaging identified some nodules in his brain. We suspected TE and began treatment successively with parenteral trimethoprim-sulfamethoxazole (TMP/SMX) plus clindamycin. After that, we switched to pyrimethamine plus sulfadiazine (PMT/SDZ) because these drugs are the first-line treatment for TE. Because the patient experienced nausea and vomiting, PMT/SDZ was replaced with TMP/SMX, atovaquone, and clindamycin. However, the patient could not tolerate them owing to their adverse reactions. Thus, we attempted oral desensitization to TMP/SMX to treat his TE. We began desensitization with 0.4/2 mg of TMP/SMX. The patient experienced morbilliform rash and elevated aminotransferase levels. Therefore, we administered a glycyrrhizin and an antihistamine and continued the last tolerable dose until these symptoms improved. After 37 days, we achieved desensitization to 160/800 mg of TMP/SMX, and the patient's symptoms improved. After using nested-polymerase chain reaction to identify T. gondii DNA in his frozen cerebrospinal fluid, which was collected at admission, his diagnosis was confirmed as TE. This might be the first case to attempt desensitization to TMP/SMX to treat TE.

摘要

刚地弓形虫是一种专性细胞内原生动物,可引起免疫功能低下患者的弓形体脑炎(TE)。我们描述了一位 29 岁的日本男性,他因头痛和呕吐就诊。他之前被诊断为人免疫缺陷病毒感染。磁共振成像在他的大脑中发现了一些结节。我们怀疑是 TE,并相继开始用静脉注射甲氧苄啶-磺胺甲恶唑(TMP/SMX)加克林霉素进行治疗。之后,我们改用乙胺嘧啶加磺胺嘧啶(PMT/SDZ),因为这些药物是 TE 的一线治疗药物。由于患者出现恶心和呕吐,PMT/SDZ 被 TMP/SMX、阿托伐醌和克林霉素取代。然而,由于不良反应,患者无法耐受这些药物。因此,我们尝试对 TMP/SMX 进行口服脱敏以治疗他的 TE。我们开始用 0.4/2 mg 的 TMP/SMX 进行脱敏。患者出现麻疹样皮疹和转氨酶水平升高。因此,我们给予甘草酸和抗组胺药物,并继续使用最后可耐受的剂量,直到这些症状改善。37 天后,我们成功地将 TMP/SMX 脱敏至 160/800 mg,患者的症状改善。在对入院时采集的冷冻脑脊液中 T. gondii DNA 进行巢式聚合酶链反应鉴定后,他的诊断被确认为 TE。这可能是首例尝试用 TMP/SMX 脱敏治疗 TE 的病例。

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