Abstract

Cerebral vasculitis is a long-standing but flourishing and fadeless research topic. Infections are a frequent cause of cerebral vasculitis, vital to diagnose due to involvement of specific anti-infection treatments. A 65-year-old man visited the hospital for his neurological symptoms without obvious inducements. After admission, radiological examination and comprehensive conventional microbiological tests (CMTs) revealed suspected intracranial infectious vasculitis. Metagenomic next-generation sequencing (mNGS) and reverse transcription-polymerase chain reaction further confirmed that his cerebral vasculitis was caused by Talaromyces marneffei (T. marneffei) and Aspergillus niger (A. niger) co-infection. The patient’s final diagnosis changed from initial herpetic encephalitis, due to the past history of cephalosome and facial herpes and non-significant antiviral therapeutic effects, to fungal cerebral vasculitis. The patient was discharged after use of targeted antifungal therapies on day 18 of his admission, and his associated symptoms disappeared completely at follow-up 3 weeks later. We first illustrated the presence of uncommon cerebral vasculitis caused by T. marneffei and A. niger in a human immunodeficiency virus-positive patient. In clinically suspected patients with infectious cerebral vasculitis, mNGS should be performed to detect potential pathogens if CMTs may not provide useful pathogenic clues, highlighting the importance of mNGS in the diagnosis and treatment of infectious diseases.

Highlights

  • Cerebral vasculitis is defined as inflammation occurring associated with destructive changes, occlusion, and infarction within the wall of intracranial blood vessels(Kraemer and Berlit 2021; Camuset et al 2012)

  • To seek for further diagnosis and treatment, he was transferred to our hospital with suspected herpetic encephalitis or arteriosclerotic cerebral infarction, considering that the patient had a past history of cephalosome, facial herpes, and type-2 diabetes

  • At follow-up 3 weeks later, the fever and neuronal disorders vanished completely. In this case, considering that the patient had a history of facial herpes and was not cured on his hospitalization, and the brain computed tomography (CT) showed the temporal lobe lesion with hemorrhage, herpetic encephalitis was considered for prediagnosis; antiviral treatment was given

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Summary

Introduction

Cerebral vasculitis is defined as inflammation occurring associated with destructive changes, occlusion, and infarction within the wall of intracranial blood vessels(Kraemer and Berlit 2021; Camuset et al 2012). A 65-year-old man without obvious inducements was hospitalized for slow response, decreased speech and dysphagia Two days ago, he went to the local hospital, and his brain computed tomography (CT) examination indicated cerebral infarction with a small amount of oozing blood. To seek for further diagnosis and treatment, he was transferred to our hospital with suspected herpetic encephalitis or arteriosclerotic cerebral infarction, considering that the patient had a past history of cephalosome, facial herpes, and type-2 diabetes. His blood pressure was 109/65 mmHg, pulse was 103 bpm, respiration was 20 bpm, and temperature was 36.8 °C on admission. Cerebrospinal fluid was obtained by lumbar puncture after admission, and antiviral therapies (Acyclovir, 500 mg, every 8 h) were given

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