Gu Hyun Jung, Kim Young Jin, Lee Hee Joo, Dong Sung Hwa, Kim Sung Wan, Huh Hee Jae, Ki Chang-Seok
Department of Laboratory Medicine, Kyung Hee University School of Medicine, 23 Kyungheedae-ro, Dongdaemun-gu, Seoul, 02447, Korea.
Department of Otolaryngology-Head and Neck Surgery, Kyung Hee University School of Medicine, Seoul, Korea.
Mycopathologia. 2016 Dec;181(11-12):901-908. doi: 10.1007/s11046-016-0062-z. Epub 2016 Sep 20.
Human Lasiodiplodia theobromae infection has not been reported frequently. We report the first case of invasive L. theobromae nasal and neck infection. A 66-year-old male visited our hospital with anemia and general weakness. He showed pancytopenia, and his bone marrow examination revealed markedly decreased hematopoietic cells. The patient was presumed to have iatrogenic aplastic anemia due to mushroom toxicity. He began treatment for multiple organ infections with broad-spectrum antibiotics and antifungal agents. During hospitalization, he complained of nasal obstruction and left neck lymph node enlargement. A mass-like lesion was observed, and a nasal mass biopsy was performed. The mass was identified as a fungal ball. He underwent surgical excision for the nasal mass and the neck lymph node. The pathologic examination indicated an invasive fungal infection, and the lymph node revealed chronic granulomatous inflammation with fungal infection. 18s rRNA sequencing revealed that the sequence shared 99 % identity with L. theobromae. The nasal mass fungus was identified by internal transcribed spacer region sequencing from pathologic paraffin sections. The obtained sequence corresponded to Lasiodiplodia or Macrophoma. The sequence corresponded to the neck discharge sequence results. Hence, the patient was diagnosed with invasive fungal sinusitis with neck lymph node involvement caused by L. theobromae. To our knowledge, this is the first report of L. theobromae infection in Korea and the first report of invasive L. theobromae fungal sinusitis in the literature. We should include more precise evaluations of additional novel fungal species as possible candidates.
人类感染可可毛色二孢菌的情况尚未频繁报道。我们报告首例侵袭性可可毛色二孢菌鼻腔及颈部感染病例。一名66岁男性因贫血和全身乏力前来我院就诊。他表现为全血细胞减少,骨髓检查显示造血细胞明显减少。该患者被推测因蘑菇中毒导致医源性再生障碍性贫血。他开始使用广谱抗生素和抗真菌药物治疗多器官感染。住院期间,他主诉鼻塞和左侧颈部淋巴结肿大。观察到一个肿块样病变,并进行了鼻腔肿块活检。肿块被确定为真菌球。他接受了鼻腔肿块和颈部淋巴结的手术切除。病理检查显示为侵袭性真菌感染,淋巴结显示伴有真菌感染的慢性肉芽肿性炎症。18s rRNA测序显示该序列与可可毛色二孢菌的序列相似度为99%。通过对病理石蜡切片进行内部转录间隔区测序鉴定了鼻腔肿块真菌。获得的序列与可可毛色二孢菌或大茎点霉相符。该序列与颈部分泌物序列结果相符。因此,该患者被诊断为侵袭性真菌性鼻窦炎伴颈部淋巴结受累,由可可毛色二孢菌引起。据我们所知,这是韩国首例可可毛色二孢菌感染报告,也是文献中首例侵袭性可可毛色二孢菌真菌性鼻窦炎报告。我们应尽可能对更多新的真菌物种进行更精确的评估。