{"title":"Cladosporium cladosporioides 脑脓肿:一个神秘的病例","authors":"Sudesh Gourav, Gagandeep Singh, Immaculata Xess, Sonakshi Gupta, Bhaskar Rana, Himanshu Mishra, Mragnayani Pandey","doi":"10.1016/j.mycmed.2024.101514","DOIUrl":null,"url":null,"abstract":"<div><div>A fifteen-year-old boy was brought to emergency department with complaints of altered sensorium, aphasia and right sided hemiparesis following severe dengue one month back. On physical examination, tone was flaccid and power was diminished in right upper and lower limbs. Reflexes were diminished in all four limbs. Magnetic resonance imaging showed multiple well defined thin walled ring-enhancing lesions in left basal ganglia, bilateral cerebellum, left occipital lobe and bilateral fronto-temporo-parietal lobes. The basal ganglia focus was tapped. Potassium hydroxide-calcofluor white mount of the intra-operative pus sample showed fragmented septate hyphae with folding and with wide variations in breadth. A provisional report of septate and aseptate hyphae suggestive of mixed infection was given. Empirical voriconazole was stopped and the patient was started on liposomal amphotericin B to cover a broader spectrum of molds. Subsequently, fungal culture of the pus sample grew off-white glabrous colonies in multiple culture tubes. On lactophenol cotton blue mount, shield cells were seen suggestive of <em>Cladosporium</em> spp. Amphotericin B was stopped after provisional identification of <em>Cladosporium</em> spp. was given by the laboratory and IV voriconazole was started. The identification was confirmed to be <em>Cladosporium cladosporioides</em> by microculture and sequencing of the internal transcribed spacer region of the 18s ribosomal DNA<em>.</em> The patient improved with drainage of the largest basal ganglia focus and voriconazole. This case exemplifies the potential of saprobic fungi to cause invasive infections in human.</div></div>","PeriodicalId":14824,"journal":{"name":"Journal de mycologie medicale","volume":null,"pages":null},"PeriodicalIF":2.2000,"publicationDate":"2024-10-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Cladosporium cladosporioides brain abscess: An enigmatic case\",\"authors\":\"Sudesh Gourav, Gagandeep Singh, Immaculata Xess, Sonakshi Gupta, Bhaskar Rana, Himanshu Mishra, Mragnayani Pandey\",\"doi\":\"10.1016/j.mycmed.2024.101514\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>A fifteen-year-old boy was brought to emergency department with complaints of altered sensorium, aphasia and right sided hemiparesis following severe dengue one month back. On physical examination, tone was flaccid and power was diminished in right upper and lower limbs. Reflexes were diminished in all four limbs. Magnetic resonance imaging showed multiple well defined thin walled ring-enhancing lesions in left basal ganglia, bilateral cerebellum, left occipital lobe and bilateral fronto-temporo-parietal lobes. The basal ganglia focus was tapped. Potassium hydroxide-calcofluor white mount of the intra-operative pus sample showed fragmented septate hyphae with folding and with wide variations in breadth. A provisional report of septate and aseptate hyphae suggestive of mixed infection was given. Empirical voriconazole was stopped and the patient was started on liposomal amphotericin B to cover a broader spectrum of molds. Subsequently, fungal culture of the pus sample grew off-white glabrous colonies in multiple culture tubes. On lactophenol cotton blue mount, shield cells were seen suggestive of <em>Cladosporium</em> spp. Amphotericin B was stopped after provisional identification of <em>Cladosporium</em> spp. was given by the laboratory and IV voriconazole was started. The identification was confirmed to be <em>Cladosporium cladosporioides</em> by microculture and sequencing of the internal transcribed spacer region of the 18s ribosomal DNA<em>.</em> The patient improved with drainage of the largest basal ganglia focus and voriconazole. 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引用次数: 0
摘要
一名 15 岁的男孩被送到急诊科,主诉一个月前因严重登革热导致感觉改变、失语和右侧偏瘫。经体格检查,他的右上肢和右下肢肌张力松弛,力量减弱。四肢反射减弱。磁共振成像显示,左侧基底节、双侧小脑、左枕叶和双侧额颞顶叶有多个界限清楚的薄壁环形强化病灶。对基底节病灶进行了探查。术中脓液样本的氢氧化钾-氟化钙白卡图显示出碎裂的隔膜菌丝,有折叠现象,宽度变化很大。临时报告显示,有隔和无隔菌丝混合感染。患者停用了伏立康唑,并开始使用两性霉素 B 脂质体,以覆盖更广泛的霉菌谱。随后,脓液样本的真菌培养在多个培养管中都长出了米白色无毛菌落。实验室初步鉴定为克拉多孢子菌属后,停用了两性霉素 B,并开始静脉注射伏立康唑。通过微生物培养和 18s 核糖体 DNA 内部转录间隔区测序,确认为 Cladosporium cladosporioides。通过引流最大的基底节病灶和使用伏立康唑,患者病情有所好转。该病例充分说明了有疮痂真菌导致人类入侵性感染的可能性。
Cladosporium cladosporioides brain abscess: An enigmatic case
A fifteen-year-old boy was brought to emergency department with complaints of altered sensorium, aphasia and right sided hemiparesis following severe dengue one month back. On physical examination, tone was flaccid and power was diminished in right upper and lower limbs. Reflexes were diminished in all four limbs. Magnetic resonance imaging showed multiple well defined thin walled ring-enhancing lesions in left basal ganglia, bilateral cerebellum, left occipital lobe and bilateral fronto-temporo-parietal lobes. The basal ganglia focus was tapped. Potassium hydroxide-calcofluor white mount of the intra-operative pus sample showed fragmented septate hyphae with folding and with wide variations in breadth. A provisional report of septate and aseptate hyphae suggestive of mixed infection was given. Empirical voriconazole was stopped and the patient was started on liposomal amphotericin B to cover a broader spectrum of molds. Subsequently, fungal culture of the pus sample grew off-white glabrous colonies in multiple culture tubes. On lactophenol cotton blue mount, shield cells were seen suggestive of Cladosporium spp. Amphotericin B was stopped after provisional identification of Cladosporium spp. was given by the laboratory and IV voriconazole was started. The identification was confirmed to be Cladosporium cladosporioides by microculture and sequencing of the internal transcribed spacer region of the 18s ribosomal DNA. The patient improved with drainage of the largest basal ganglia focus and voriconazole. This case exemplifies the potential of saprobic fungi to cause invasive infections in human.
期刊介绍:
The Journal de Mycologie Medicale / Journal of Medical Mycology (JMM) publishes in English works dealing with human and animal mycology. The subjects treated are focused in particular on clinical, diagnostic, epidemiological, immunological, medical, pathological, preventive or therapeutic aspects of mycoses. Also covered are basic aspects linked primarily with morphology (electronic and photonic microscopy), physiology, biochemistry, cellular and molecular biology, immunochemistry, genetics, taxonomy or phylogeny of pathogenic or opportunistic fungi and actinomycetes in humans or animals. Studies of natural products showing inhibitory activity against pathogenic fungi cannot be considered without chemical characterization and identification of the compounds responsible for the inhibitory activity.
JMM publishes (guest) editorials, original articles, reviews (and minireviews), case reports, technical notes, letters to the editor and information. Only clinical cases with real originality (new species, new clinical present action, new geographical localization, etc.), and fully documented (identification methods, results, etc.), will be considered.
Under no circumstances does the journal guarantee publication before the editorial board makes its final decision.
The journal is indexed in the main international databases and is accessible worldwide through the ScienceDirect and ClinicalKey platforms.