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First case of invasive Rasamsonia argillacea in a child with chronic granulomatous disease in Qatar 卡塔尔首例慢性肉芽肿病患儿中的侵袭性Rasamsonia argillacea病例
IF 1.6
Medical Mycology Case Reports Pub Date : 2024-10-09 DOI: 10.1016/j.mmcr.2024.100675
Nada Shurab , Anju Sharma , Eman Al Maslamani , Andrés Pérez-López , Osamah Al Walid , Mohammed Suleiman
{"title":"First case of invasive Rasamsonia argillacea in a child with chronic granulomatous disease in Qatar","authors":"Nada Shurab ,&nbsp;Anju Sharma ,&nbsp;Eman Al Maslamani ,&nbsp;Andrés Pérez-López ,&nbsp;Osamah Al Walid ,&nbsp;Mohammed Suleiman","doi":"10.1016/j.mmcr.2024.100675","DOIUrl":"10.1016/j.mmcr.2024.100675","url":null,"abstract":"<div><div>Invasive fungal infections (IFI) are a major cause of mortality and morbidity in patients with chronic granulomatous disease (CGD). We report and comment on a case of IFI caused by <em>Rasamsonia argillacea</em> in a 16-year-old female with CGD. Additionally, we briefly review and discuss the most challenging aspects of the identification and treatment of this species.</div></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"46 ","pages":"Article 100675"},"PeriodicalIF":1.6,"publicationDate":"2024-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142421827","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A case of flexor tenosynovitis caused by Cyberlindnera rhodanensis – First reported human infection 一例由 Cyberlindnera rhodanensis 引起的屈肌腱鞘炎 - 首次报告的人类感染病例
IF 1.6
Medical Mycology Case Reports Pub Date : 2024-10-05 DOI: 10.1016/j.mmcr.2024.100673
Sarah Kim, Stephanie Spivack
{"title":"A case of flexor tenosynovitis caused by Cyberlindnera rhodanensis – First reported human infection","authors":"Sarah Kim,&nbsp;Stephanie Spivack","doi":"10.1016/j.mmcr.2024.100673","DOIUrl":"10.1016/j.mmcr.2024.100673","url":null,"abstract":"<div><div>We report a case of an immunocompetent individual who was diagnosed with fungal tenosynovitis of the wrist caused by <em>Cyberlindnera rhodanensis</em>, a yeast in the Saccharomycetales order that has never been reported to cause infections in humans. The yeast grew in routine culture and was sent to a reference laboratory for identification and susceptibility testing. The patient ultimately received six surgeries and five months of antifungal therapy, including micafungin and voriconazole, before clinical resolution.</div></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"46 ","pages":"Article 100673"},"PeriodicalIF":1.6,"publicationDate":"2024-10-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142421769","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Extensive erythematous plaques of fungal origin in an overseas student: Cutaneous manifestation of coccidioidomycosis 一名海外留学生患上真菌引起的大面积红斑：球孢子菌病的皮肤表现
IF 1.6
Medical Mycology Case Reports Pub Date : 2024-10-01 DOI: 10.1016/j.mmcr.2024.100674
Qi-Hao Yao , Xiu-Jiao Xia , Hui-Lin Zhi , Ze-Hu Liu
{"title":"Extensive erythematous plaques of fungal origin in an overseas student: Cutaneous manifestation of coccidioidomycosis","authors":"Qi-Hao Yao ,&nbsp;Xiu-Jiao Xia ,&nbsp;Hui-Lin Zhi ,&nbsp;Ze-Hu Liu","doi":"10.1016/j.mmcr.2024.100674","DOIUrl":"10.1016/j.mmcr.2024.100674","url":null,"abstract":"<div><div>We present a case of <em>Coccidioides posadasii</em> infection which was contracted during study abroad. This coccidioidomycosis showed atypical manifestations and was diagnosed by a combination of tissue biopsy, metagenomic next–generation sequencing, internal transcribed spacer sequencing and culture. Initial treatment with fluconazole was not effective. Antifungal therapy was switched to voriconazole based on drug sensitivity results with good result. This case demonstrates the clinical significance of combining multiple diagnostic methods.</div></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"46 ","pages":"Article 100674"},"PeriodicalIF":1.6,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142421768","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Invasive fungal otitis media with peripheral facial paralysis 伴有周围性面瘫的侵袭性真菌中耳炎
IF 1.6
Medical Mycology Case Reports Pub Date : 2024-09-27 DOI: 10.1016/j.mmcr.2024.100672
Wenjie Kang , Jie Zhang , Hanbing Gao , Ming Guan
{"title":"Invasive fungal otitis media with peripheral facial paralysis","authors":"Wenjie Kang ,&nbsp;Jie Zhang ,&nbsp;Hanbing Gao ,&nbsp;Ming Guan","doi":"10.1016/j.mmcr.2024.100672","DOIUrl":"10.1016/j.mmcr.2024.100672","url":null,"abstract":"<div><div>Invasive fungal otitis media is clinically rare and diagnosis often delayed. We report a 65-year-old female with <em>Aspergillus fumigatus</em> otitis media complicated by mastoiditis and peripheral facial paralysis. Complete mastoidectomy and type II tympanoplasty, with oral administration of voriconazole for more than 3 months resulted in a successful outcome.</div></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"46 ","pages":"Article 100672"},"PeriodicalIF":1.6,"publicationDate":"2024-09-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142421767","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Osteoarticular mucormycosis of the distal femur in a post COVID-19 patient 一名 COVID-19 后患者的股骨远端骨关节粘液瘤病
IF 1.6
Medical Mycology Case Reports Pub Date : 2024-09-16 DOI: 10.1016/j.mmcr.2024.100670
Srinivas Kasha , Venugopal Palakurthi , Ranjith Kumar Yalamanchili , Patil Pratik Yashavant , Rohith GPRK
{"title":"Osteoarticular mucormycosis of the distal femur in a post COVID-19 patient","authors":"Srinivas Kasha ,&nbsp;Venugopal Palakurthi ,&nbsp;Ranjith Kumar Yalamanchili ,&nbsp;Patil Pratik Yashavant ,&nbsp;Rohith GPRK","doi":"10.1016/j.mmcr.2024.100670","DOIUrl":"10.1016/j.mmcr.2024.100670","url":null,"abstract":"<div><div>A 38 year old man with no known comorbidities presented with pain and swelling over the knee joint a few days after recovery from severe COVID-19. Initial debridement and cultures revealed growth of Mucorales affecting a large segment of the distal femur with also positive cultures obtained from the maxillary sinus and the lower lobe of the right lung. Due to this involvement of a long segment of the femur, right lung and left maxillary sinus, a multidisciplinary approach of above knee amputation along with debridement of left maxillary sinus and lobectomy of right lung lower lobe was performed to decrease the fungal load and favour good prognosis. This report warrants the need for early imaging and surgical debridement of tissue for fungal cultures and biopsy in immunocompromised individuals.</div></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"46 ","pages":"Article 100670"},"PeriodicalIF":1.6,"publicationDate":"2024-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142357607","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Miliary coccidioidomycosis mimicking tuberculosis: Case report and review of literature 模仿肺结核的球孢子菌病：病例报告和文献综述
IF 1.6
Medical Mycology Case Reports Pub Date : 2024-09-13 DOI: 10.1016/j.mmcr.2024.100668
Oscar E. Gallardo-Huizar , Joyce Lee , Kailyn Kim , Arthur C. Jeng
{"title":"Miliary coccidioidomycosis mimicking tuberculosis: Case report and review of literature","authors":"Oscar E. Gallardo-Huizar ,&nbsp;Joyce Lee ,&nbsp;Kailyn Kim ,&nbsp;Arthur C. Jeng","doi":"10.1016/j.mmcr.2024.100668","DOIUrl":"10.1016/j.mmcr.2024.100668","url":null,"abstract":"<div><p>Miliary coccidioidomycosis is a severe manifestation of diseases caused by <em>Coccidioides immitis</em> and <em>Coccidioides posadasii</em> that is endemic to the southwestern United States as well as Central and South America. While most cases of coccidioidomycosis present with pulmonary disease, certain risk factors increase the risk for disseminated disease. We present a case of miliary coccidioidomycosis in a 46-year-old patient with uncontrolled diabetes. Additionally, we review the features of thirty-seven cases of patients with miliary coccidioidomycosis.</p></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"46 ","pages":"Article 100668"},"PeriodicalIF":1.6,"publicationDate":"2024-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2211753924000423/pdfft?md5=156b3f4699098efba953fdf89dab80a2&pid=1-s2.0-S2211753924000423-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142229842","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A case of refractory onychomycosis caused by Kloeckera apiculata: Successful treatment with itraconazole 一例由 Kloeckera apiculata 引起的难治性甲癣：伊曲康唑的成功治疗
IF 1.6
Medical Mycology Case Reports Pub Date : 2024-09-11 DOI: 10.1016/j.mmcr.2024.100669
Samantha S. Ehrlich-Fein , Samir B. Patel
{"title":"A case of refractory onychomycosis caused by Kloeckera apiculata: Successful treatment with itraconazole","authors":"Samantha S. Ehrlich-Fein ,&nbsp;Samir B. Patel","doi":"10.1016/j.mmcr.2024.100669","DOIUrl":"10.1016/j.mmcr.2024.100669","url":null,"abstract":"<div><p>Here, we present the case of an otherwise healthy patient, without risk factors, who developed a refractory case of onychomycosis caused by <em>Kloeckera apiculata</em>, an uncommon human pathogen. The diagnosis was ultimately confirmed by fungal nail plate culture, histopathology, and PCR. Whereas prior treatments with topical 5 % tavaborole solution, oral terbinafine, and oral fluconazole were ineffective, complete clinical and mycological cure was achieved with a 3-month course of oral itraconazole.</p></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"46 ","pages":"Article 100669"},"PeriodicalIF":1.6,"publicationDate":"2024-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2211753924000435/pdfft?md5=0420fe6354c800177ac310de5cbcd22a&pid=1-s2.0-S2211753924000435-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142229841","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Sporotrichosis caused by Sporotrix globosa in an elderly male farmer at the site of a cat scratch 一名老年男性农民被猫抓伤后引发的球孢子虫病
IF 1.6
Medical Mycology Case Reports Pub Date : 2024-09-06 DOI: 10.1016/j.mmcr.2024.100667
Yuka Sakai , Yuta Norimatsu , Taro Akatsuka , Toshihisa Hamada , Harumi Gomi , Makoto Sugaya
{"title":"Sporotrichosis caused by Sporotrix globosa in an elderly male farmer at the site of a cat scratch","authors":"Yuka Sakai ,&nbsp;Yuta Norimatsu ,&nbsp;Taro Akatsuka ,&nbsp;Toshihisa Hamada ,&nbsp;Harumi Gomi ,&nbsp;Makoto Sugaya","doi":"10.1016/j.mmcr.2024.100667","DOIUrl":"10.1016/j.mmcr.2024.100667","url":null,"abstract":"<div><p>We report a case of sporotrichosis in an elderly male farmer at the site of a cat scratch scar.</p><p>An 84-year-old Japanese farmer was scratched by his cat two months before his visit to our hospital.</p><p>A skin biopsy was performed. Tissue culture revealed the presence of <em>Sporothrix globosa</em>.</p><p>The patient was treated with oral itraconazole 200 mg/day for 13 months due to a slow healing ulceration, and the symptoms resolved. (71 words).</p></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"46 ","pages":"Article 100667"},"PeriodicalIF":1.6,"publicationDate":"2024-09-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2211753924000411/pdfft?md5=d314790347c88ee336a5c6284d3c7f80&pid=1-s2.0-S2211753924000411-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142163235","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Meningeal sporotrichosis in an immunocompetent host: A case report 免疫功能正常宿主的脑膜孢子丝菌病：病例报告
IF 1.6
Medical Mycology Case Reports Pub Date : 2024-09-01 DOI: 10.1016/j.mmcr.2024.100665
Victor Teatini Ribeiro , Rachel Basques Caligiorne , Aldrin Pedroza Martins , Antônio Pereira Gomes Neto , Paulo Pereira Christo
{"title":"Meningeal sporotrichosis in an immunocompetent host: A case report","authors":"Victor Teatini Ribeiro ,&nbsp;Rachel Basques Caligiorne ,&nbsp;Aldrin Pedroza Martins ,&nbsp;Antônio Pereira Gomes Neto ,&nbsp;Paulo Pereira Christo","doi":"10.1016/j.mmcr.2024.100665","DOIUrl":"10.1016/j.mmcr.2024.100665","url":null,"abstract":"<div><p>A 78-year-old woman presented to hospital with altered mental status. Hyponatremia was diagnosed and treated. She maintained mental confusion despite normal sodium. No headache, fever or focal signs were present. CSF analysis showed chronic meningitis; MRI demonstrated basilar enhancement. She was empirically treated for tuberculosis, with no improvement. PCR for <em>Sporothrix</em> in the CSF was positive. After treatment with Amphotericin followed by oral itraconazole, she completely recovered her cognitive abilities. Follow-up CSF was normal. This report illustrates the need to consider sporotrichosis in the differential diagnosis of chronic meningitis in immunocompetent, and the importance of PCR as a diagnostic tool.</p></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"45 ","pages":"Article 100665"},"PeriodicalIF":1.6,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2211753924000393/pdfft?md5=87f779cac484c1888ea96b8fe682203e&pid=1-s2.0-S2211753924000393-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142149331","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Primary treatment of chronic pulmonary aspergillosis with weekly liposomal amphotericin B: A case report from Uganda 每周使用两性霉素 B 脂质体初治慢性肺曲霉菌病：乌干达的病例报告
IF 1.6
Medical Mycology Case Reports Pub Date : 2024-08-27 DOI: 10.1016/j.mmcr.2024.100666
Winnie Kibone , Felix Bongomin , David W. Denning , David B. Meya
{"title":"Primary treatment of chronic pulmonary aspergillosis with weekly liposomal amphotericin B: A case report from Uganda","authors":"Winnie Kibone ,&nbsp;Felix Bongomin ,&nbsp;David W. Denning ,&nbsp;David B. Meya","doi":"10.1016/j.mmcr.2024.100666","DOIUrl":"10.1016/j.mmcr.2024.100666","url":null,"abstract":"<div><p>Chronic pulmonary aspergillosis (CPA) treatment in Africa remains unexplored. We present a 23-year-old Ugandan male, previously treated thrice for pulmonary tuberculosis, developing CPA. Imaging showed lung fibrosis, bronchiectasis, and a fungal ball. He received weekly 600mg (10mg/kg) of liposomal amphotericin B for six weeks, leading to marked clinical improvement. Weekly liposomal amphotericin B may be a viable treatment option for CPA in resource-limited settings.</p></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"46 ","pages":"Article 100666"},"PeriodicalIF":1.6,"publicationDate":"2024-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S221175392400040X/pdfft?md5=869eeb1f4620398c42e0bdd62fda606c&pid=1-s2.0-S221175392400040X-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142229852","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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