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中枢神经系统毛霉病合并血液系统恶性肿瘤 1 例并文献复习

Central nervous system mucormycosis in a patient with hematological malignancy: A case report and review of the literature.

机构信息

Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital, Honkomagome 3-18-22, Bunkyo-ku, Tokyo, 1138677, Japan.

Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital, Honkomagome 3-18-22, Bunkyo-ku, Tokyo, 1138677, Japan.

出版信息

J Infect Chemother. 2022 Dec;28(12):1658-1662. doi: 10.1016/j.jiac.2022.08.003. Epub 2022 Aug 10.

DOI:10.1016/j.jiac.2022.08.003
PMID:35963603
Abstract

Invasive mucormycosis is a refractory fungal infection. Central nervous system (CNS) mucormycosis is a rare complication caused by infiltration from the paranasal sinuses or hematogenous dissemination. Here, we present a case of a brain abscess, due to mucormycosis, diagnosed using burr craniotomy. A 25-year-old Japanese woman with relapsed-refractory acute lymphoblastic leukemia underwent cord blood transplantation (CBT). The patient experienced prolonged and profound neutropenia, and oral voriconazole was administered as primary antifungal prophylaxis. The patient received a conditioning regimen on day -11 and complained of aphasia and right hemiparesis on day -6. Magnetic resonance imaging (MRI) revealed a T2-weighted high-intensity area in the left frontal cortex. A brain abscess was suspected, and liposomal amphotericin B (L-AMB) administration was started. The patient underwent CBT as scheduled and underwent neutrophil engraftment on day 14. Although the patient achieved complete remission on day 28, her consciousness level gradually deteriorated. MRI revealed an enlarged brain lesion with a midline shift sign, suggesting brain herniation. Craniotomy was performed to relieve intracranial pressure and drain the abscess on day 38, and a diagnosis of cerebral mucormycosis was confirmed. The L-AMB dose was increased to 10 mg/kg on day 43. Although the patient's consciousness level improved, she died of hemorrhagic cystitis and aspiration pneumonia. Cerebral mucormycosis should be suspected if neurological symptoms are observed in stem cell transplant recipients. Prompt commencement of antifungal therapy and debridement are crucial because mucormycosis has a poor prognosis.

摘要

侵袭性毛霉菌病是一种难治性真菌感染。中枢神经系统(CNS)毛霉菌病是一种罕见的并发症,由来自鼻窦或血行播散的浸润引起。在这里,我们报告了一例因毛霉菌引起的脑脓肿病例,该病例通过颅骨钻孔术确诊。一名 25 岁的日本女性患有复发性难治性急性淋巴细胞白血病,接受了脐带血移植(CBT)。患者经历了长时间和严重的中性粒细胞减少症,并给予口服伏立康唑作为原发性抗真菌预防。患者于-11 天接受了预处理方案,并于-6 天出现言语不清和右侧偏瘫。磁共振成像(MRI)显示左额叶皮质 T2 加权高信号区。怀疑脑脓肿,并开始给予脂质体两性霉素 B(L-AMB)治疗。患者按计划接受 CBT,并于第 14 天进行中性粒细胞植入。尽管患者在第 28 天达到完全缓解,但她的意识水平逐渐恶化。MRI 显示病变大脑增大,伴有中线移位征,提示脑疝。第 38 天进行了开颅手术以减轻颅内压并引流脓肿,并确诊为脑毛霉菌病。第 43 天,L-AMB 剂量增加至 10mg/kg。尽管患者的意识水平有所改善,但她死于出血性膀胱炎和吸入性肺炎。如果在干细胞移植受者中观察到神经症状,应怀疑脑毛霉菌病。尽早开始抗真菌治疗和清创至关重要,因为毛霉菌病预后不良。

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