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Invasive cerebral aspergillosis in non-neutropenic patients: A case series from Western India
被引:0
|作者:
Samantaray, Subhashree
[1
]
Kumar, Deepak
[1
]
Meena, Durga Shankar
Bohra, Gopal Krishana
[1
]
Akshatha, R.
[1
]
Jain, Vidhi
[2
]
Tiwari, Sarbesh
[3
]
Balamurugan, T.
[4
]
Midha, Naresh
[1
]
Garg, Mahendra Kumar
[1
]
机构:
[1] All India Inst Med Sci, Dept Gen Med Infect Dis, Jodhpur, Rajasthan, India
[2] All India Inst Med Sci, Dept Microbiol, Jodhpur, Rajasthan, India
[3] All India Inst Med Sci, Dept Diagnost & Intervent Radiol, Jodhpur, Rajasthan, India
[4] All India Inst Med Sci, Dept Pathol & lab Med, Jodhpur, Rajasthan, India
来源:
JOURNAL DE MYCOLOGIE MEDICALE
|
2023年
/
33卷
/
02期
关键词:
Invasive cerebral aspergillosis;
Non-neutropenic patients;
CSF galactomannan;
Voriconazole;
CENTRAL-NERVOUS-SYSTEM;
GALACTOMANNAN ANTIGEN;
DIAGNOSIS;
D O I:
10.1016/j.mycmed.2023.101380
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Purpose: Invasive cerebral aspergillosis (ICA) is a rare but fatal infection affecting neutropenic immunocompromised patients. Recently cases have been reported in non-neutropenic settings also. We hereby present a series of ICA cases in non-neutropenic patients diagnosed at our tertiary care centre in Western India between March to October 2021. Methods: All patients with clinico-radiological suspicion of CNS infections were analysed. Data regarding Clinico-radiological features, diagnosis, treatment and outcome were collected. After ruling out bacterial, viral and mycobacterial causes, appropriate samples were sent for KOH (potassium hydroxide) wet mount, fungal culture, histopathology and serum/CSF galactomannan. Results: A total of four patients were diagnosed with ICA with a mean age of 43.5 years. Three patients had significant comorbidities; Diabetes mellitus, chronic liver disease and COVID-19 pneumonia treated with dexamethasone, respectively. One patient had no known predisposing factor. Radiologically, one patient presented with a frontal brain abscess and two patients had multiple subcortical hyperintensities. Three patients were diagnosed based on CSF galactomannan (PlateliaTM Aspergillus antigen, Bio-Rad, France) with OD >1 and one patient had high serum galactomannan (OD >2). CSF culture grew Aspergillus species in two patients. All patients were treated with Voriconazole. One patient recovered, and the remaining three succumbed due to delayed presentation and extensive cerebral involvement. Conclusion: Even in non-neutropenic patients, a high index of suspicion is warranted for cerebral aspergillosis. CSF galactomannan can be considered a reliable marker for diagnosing ICA in non-neutropenic settings. Early diagnosis allows timely antifungal therapy, which could be a key to improving the outcomes. (c) 2023 SFMM. Published by Elsevier Masson SAS. All rights reserved.
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