We provide the first case report of peritoneal dialysis (PD)-associated peritonitis due to Lasiodiplodia theobromae, a known plant pathogen causing rotting and dieback in post-harvest citrus fruit, in immunocompetent patient with fungal colonization inside the PD catheter lumen. A root cause analysis suspected the patient's umbilical infection as the source of contamination. The fungal infection was established through microscopic examination of the PD catheter lumen and galactomannan testing in both serum and effluent. The species of pathogen was confirmed by DNA barcoding. The patient responded well to timely PD catheter removal and a 2-week course of oral voriconazole. Preventive strategies should prioritize hygiene practices, including umbilical care, to mitigate the risk of contamination and subsequent infections of fungal pathogens.
我们提供了首例腹膜透析(PD)患者腹膜透析导管腔内真菌定植引起腹膜透析相关腹膜炎的病例报告。根本原因分析怀疑患者的脐部感染是污染源。通过对腹膜透析导管管腔进行显微镜检查以及对血清和流出物进行半乳甘露聚糖检测,确定了真菌感染。病原体的种类通过 DNA 条形码得到确认。及时拔除腹膜透析导管并口服伏立康唑两周后,患者反应良好。预防策略应优先考虑卫生习惯,包括脐部护理,以降低真菌病原体污染和后续感染的风险。
{"title":"Peritoneal dialysis-associated peritonitis due to infected umbilicus","authors":"Veerapat Wattanasatja , Jarubut Phisutrattanaporn , Natchaporn Doenphai , Sirirat Sirinual , Talerngsak Kanjanabuch","doi":"10.1016/j.mmcr.2024.100654","DOIUrl":"10.1016/j.mmcr.2024.100654","url":null,"abstract":"<div><p>We provide the first case report of peritoneal dialysis (PD)-associated peritonitis due to <em>Lasiodiplodia theobromae</em>, a known plant pathogen causing rotting and dieback in post-harvest citrus fruit, in immunocompetent patient with fungal colonization inside the PD catheter lumen. A root cause analysis suspected the patient's umbilical infection as the source of contamination. The fungal infection was established through microscopic examination of the PD catheter lumen and galactomannan testing in both serum and effluent. The species of pathogen was confirmed by DNA barcoding. The patient responded well to timely PD catheter removal and a 2-week course of oral voriconazole. Preventive strategies should prioritize hygiene practices, including umbilical care, to mitigate the risk of contamination and subsequent infections of fungal pathogens.</p></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"45 ","pages":"Article 100654"},"PeriodicalIF":2.2,"publicationDate":"2024-06-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2211753924000289/pdfft?md5=67f689115adc9d97bb2904a2bd192c58&pid=1-s2.0-S2211753924000289-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141410188","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}
We present the first case report of peritoneal dialysis (PD)-associated peritonitis due to Gibellulopsis nigrescens, with the same pathogen detected in her caregiver's tinea capitis. This confirms that touch contamination from the caregiver's infection was the primary source of this rare organism. The species of pathogen causing peritonitis and her caregiver's scalp lesions were identified by DNA barcoding. The patient responded well to timely PD catheter removal and a 2-week course of systemic amphotericin B deoxycholate. Preventive strategies should prioritize hygiene practices, including maintaining adequate personal hygiene and practicing thorough hand washing, to mitigate the risk of touch contamination and subsequent infection with fungal pathogens.
我们报告了首例腹膜透析(PD)相关腹膜炎病例,该病例的病原体是由Gibellulopsis nigrescens引起的,而在其护理者的癣菌中也检测到了相同的病原体。这证实了护理人员感染的接触性污染是这种罕见病菌的主要来源。通过 DNA 条形码,确定了引起腹膜炎的病原体种类及其护理人员的头皮病变。及时拔除腹膜透析导管并全身使用两性霉素 B 脱氧胆酸盐两周后,患者反应良好。预防策略应优先考虑卫生习惯,包括保持充分的个人卫生和彻底洗手,以降低接触污染和随后感染真菌病原体的风险。
{"title":"Caregiver skin infection causing peritoneal dialysis-associated peritonitis","authors":"Rutchanee Chieochanthanakij , Veerapat Wattanasatja , Panthira Passorn , Dhammika Leshan Wannigama , Talerngsak Kanjanabuch","doi":"10.1016/j.mmcr.2024.100653","DOIUrl":"https://doi.org/10.1016/j.mmcr.2024.100653","url":null,"abstract":"<div><p>We present the first case report of peritoneal dialysis (PD)-associated peritonitis due to <em>Gibellulopsis nigrescens</em>, with the same pathogen detected in her caregiver's tinea capitis. This confirms that touch contamination from the caregiver's infection was the primary source of this rare organism. The species of pathogen causing peritonitis and her caregiver's scalp lesions were identified by DNA barcoding. The patient responded well to timely PD catheter removal and a 2-week course of systemic amphotericin B deoxycholate. Preventive strategies should prioritize hygiene practices, including maintaining adequate personal hygiene and practicing thorough hand washing, to mitigate the risk of touch contamination and subsequent infection with fungal pathogens.</p></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"44 ","pages":"Article 100653"},"PeriodicalIF":2.2,"publicationDate":"2024-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2211753924000277/pdfft?md5=20137061a4d804a40f339242af53443f&pid=1-s2.0-S2211753924000277-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141244068","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}
Pub Date : 2024-05-08DOI: 10.1016/j.mmcr.2024.100652
Jiří Řehulka , Vit Hubka
Spontaneous mycosis caused by Aureobasidium pullulans is documented in roach in a cyprinid-prevalent water reservoir in Czechia. Gross pathological lesions included pale gills and splenomegaly, as revealed during necropsy examination. Histological examination showed extensive foci with fungal elements in the kidney. The isolated fungus was identified through phenotypic and molecular characterization, including phylogeny. This report represents the first case of A. pullulans infection in fish and cold-blooded vertebrates, to the best of our knowledge.
在捷克的一个鲤科鱼类盛行的水库中,记录了蟑螂因Aureobasidium pullulans引起的自发性霉菌病。尸体解剖检查发现,大体病理变化包括鳃苍白和脾肿大。组织学检查显示,肾脏中有大量带有真菌成分的病灶。通过表型和分子鉴定,包括系统发育,确定了分离出的真菌。据我们所知,本报告是鱼类和冷血脊椎动物感染 A. pullulans 的首例病例。
{"title":"A renal mycosis of roach (Rutilus rutilus) caused by the Aureobasidium pullulans","authors":"Jiří Řehulka , Vit Hubka","doi":"10.1016/j.mmcr.2024.100652","DOIUrl":"https://doi.org/10.1016/j.mmcr.2024.100652","url":null,"abstract":"<div><p>Spontaneous mycosis caused by <em>Aureobasidium pullulans</em> is documented in roach in a cyprinid-prevalent water reservoir in Czechia. Gross pathological lesions included pale gills and splenomegaly, as revealed during necropsy examination. Histological examination showed extensive foci with fungal elements in the kidney. The isolated fungus was identified through phenotypic and molecular characterization, including phylogeny. This report represents the first case of <em>A. pullulans</em> infection in fish and cold-blooded vertebrates, to the best of our knowledge.</p></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"44 ","pages":"Article 100652"},"PeriodicalIF":2.2,"publicationDate":"2024-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2211753924000265/pdfft?md5=6f310f1c4b266cfa0dda3e5097d51f48&pid=1-s2.0-S2211753924000265-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140951783","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}
Pub Date : 2024-05-01DOI: 10.1016/j.mmcr.2024.100651
Dan Zhang , Guofeng Mao , Meichun Liang , Guiqin Sun , Debao Yu
Aspergillus peritonitis is a rare but highly severe complication of peritoneal dialysis with a high mortality rate. We report a case of Aspergillus fumigatus peritonitis. Despite early removal of the catheter and oral voriconazole antifungal treatment for 3 weeks, the treatment effect was unsatisfactory, resulting in prolonged hospital stay and affecting the patient's quality of life. After switching to liposomalAmphotericin B, inflammation indicators rapidly decreased and infection was controlled. Liposomalamphotericin B provides an option for treatment of Aspergillus peritonitis.
曲霉菌腹膜炎是腹膜透析的一种罕见但非常严重的并发症,死亡率很高。我们报告了一例曲霉菌腹膜炎病例。尽管患者及早拔除导管并口服伏立康唑抗真菌治疗 3 周,但治疗效果并不理想,导致住院时间延长,影响了患者的生活质量。改用两性霉素 B 脂质体后,炎症指标迅速下降,感染得到控制。两性霉素 B 脂质体为治疗曲霉菌腹膜炎提供了一种选择。
{"title":"Diagnosis and treatment of peritoneal dialysis associated mycotic peritonitis caused by Aspergillus fumigatus infection","authors":"Dan Zhang , Guofeng Mao , Meichun Liang , Guiqin Sun , Debao Yu","doi":"10.1016/j.mmcr.2024.100651","DOIUrl":"https://doi.org/10.1016/j.mmcr.2024.100651","url":null,"abstract":"<div><p><em>Aspergillus</em> peritonitis is a rare but highly severe complication of peritoneal dialysis with a high mortality rate. We report a case of <em>Aspergillus fumigatus</em> peritonitis. Despite early removal of the catheter and oral voriconazole antifungal treatment for 3 weeks, the treatment effect was unsatisfactory, resulting in prolonged hospital stay and affecting the patient's quality of life. After switching to liposomalAmphotericin B, inflammation indicators rapidly decreased and infection was controlled. Liposomalamphotericin B provides an option for treatment of <em>Aspergillus</em> peritonitis.</p></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"44 ","pages":"Article 100651"},"PeriodicalIF":2.2,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2211753924000253/pdfft?md5=4bb80f7fa94a6cb5ebe47ce90de2d636&pid=1-s2.0-S2211753924000253-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140823715","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}
Pub Date : 2024-04-27DOI: 10.1016/j.mmcr.2024.100650
Mariamalia Cob , Luisa F. López , D. Joseph Sexton , Adrián Fallas , Juan David Muñoz , Ricardo Gutiérrez
Phaeoacremonium is a genus of dematiaceous fungi that rarely causes human infections. We describe a case of subcutaneous infection in a 70-year-old diabetic man with lesions on the dorsum of the one foot. The agent was isolated, and for the final identification we performed matrix-assisted laser desorption ionization–time of flight mass spectrometry (MALDI-TOF MS) and DNA sequencing. After diagnosis, the patient underwent curettage of the cyst and received 100mg of Itraconazole, twice daily for 6 months. Clinical resolution of the lesion was observed after treatment. This is the first case of infection by Phaeoacremonium venezuelense reported in Costa Rica.
{"title":"Subcutaneous phaeohyphomycosis due to Phaeoacremonium venezuelense: The first clinical case report in Costa Rica","authors":"Mariamalia Cob , Luisa F. López , D. Joseph Sexton , Adrián Fallas , Juan David Muñoz , Ricardo Gutiérrez","doi":"10.1016/j.mmcr.2024.100650","DOIUrl":"https://doi.org/10.1016/j.mmcr.2024.100650","url":null,"abstract":"<div><p><em>Phaeoacremonium</em> is a genus of dematiaceous fungi that rarely causes human infections. We describe a case of subcutaneous infection in a 70-year-old diabetic man with lesions on the dorsum of the one foot. The agent was isolated, and for the final identification we performed matrix-assisted laser desorption ionization–time of flight mass spectrometry (MALDI-TOF MS) and DNA sequencing. After diagnosis, the patient underwent curettage of the cyst and received 100mg of Itraconazole, twice daily for 6 months. Clinical resolution of the lesion was observed after treatment. This is the first case of infection by <em>Phaeoacremonium venezuelense</em> reported in Costa Rica.</p></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"44 ","pages":"Article 100650"},"PeriodicalIF":2.2,"publicationDate":"2024-04-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2211753924000241/pdfft?md5=555e1c7cf8ac709966a0e047b2fbfabb&pid=1-s2.0-S2211753924000241-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140816125","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}
Pub Date : 2024-04-14DOI: 10.1016/j.mmcr.2024.100649
Katrina J. Villegas MD , Nagihan Orhun MD , Sebastian Vera Garces , Sacide S. Ozgur MD , Patrick Michael MD , Ali Zahran MD , Daniel Rabinowitz MD
A 46-year-old diabetic woman with unilateral renal fungus ball was successfully treated with antifungal therapy, endoscopic extraction and ureteral stent placement. The patient was initially treated for a right staghorn calculus, thereafter developed urinary symptoms. Imaging revealed distal left ureter filling defects and a previous stent at the ureteropelvic junction. Urine culture confirmed Candida glabrata sensitive to Micafungin. Bilateral ureteroscopy facilitated the extraction of a left renal pelvis fungus ball. This case underscores the challenges in diagnosing fungal UTIs in patients with predisposing factors, and highlights a combined medical and surgical approach for effective treatment of renal fungus balls.
{"title":"Unilateral renal fungus ball caused by Candida glabrata","authors":"Katrina J. Villegas MD , Nagihan Orhun MD , Sebastian Vera Garces , Sacide S. Ozgur MD , Patrick Michael MD , Ali Zahran MD , Daniel Rabinowitz MD","doi":"10.1016/j.mmcr.2024.100649","DOIUrl":"https://doi.org/10.1016/j.mmcr.2024.100649","url":null,"abstract":"<div><p>A 46-year-old diabetic woman with unilateral renal fungus ball was successfully treated with antifungal therapy, endoscopic extraction and ureteral stent placement. The patient was initially treated for a right staghorn calculus, thereafter developed urinary symptoms. Imaging revealed distal left ureter filling defects and a previous stent at the ureteropelvic junction. Urine culture confirmed <em>Candida glabrata</em> sensitive to Micafungin. Bilateral ureteroscopy facilitated the extraction of a left renal pelvis fungus ball. This case underscores the challenges in diagnosing fungal UTIs in patients with predisposing factors, and highlights a combined medical and surgical approach for effective treatment of renal fungus balls.</p></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"44 ","pages":"Article 100649"},"PeriodicalIF":2.2,"publicationDate":"2024-04-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S221175392400023X/pdfft?md5=b22b9ba7f14135abf192c8dacb011684&pid=1-s2.0-S221175392400023X-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140558665","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}
Pub Date : 2024-04-10DOI: 10.1016/j.mmcr.2024.100647
Muhammad Rizwan Zafar , Thomas Whitfield , Sabeen Khurshid Zaidi , Sanjeewani Weerakoon , Joel Paul , Riina Rautemaa-Richardson
Fungal infections can be challenging to diagnose in returning travellers due to their non-specific clinical manifestations and changing epidemiology. We present a case of progressive disseminated histoplasmosis in a returning traveller from Bangladesh. The patient had a progressive and prolonged respiratory illness necessitating mechanical ventilatory support. The clue to potential fungal aetiology was provided by serum fungal markers - 1-3-β-D-glucan and Aspergillus galactomannan. Diagnosis was eventually made using panfungal PCR on bronchioalveolar lavage fluid.
{"title":"Histoplasma capsulatum as a cause for prolonged pulmonary illness in an immunocompetent returning traveller from Bangladesh","authors":"Muhammad Rizwan Zafar , Thomas Whitfield , Sabeen Khurshid Zaidi , Sanjeewani Weerakoon , Joel Paul , Riina Rautemaa-Richardson","doi":"10.1016/j.mmcr.2024.100647","DOIUrl":"https://doi.org/10.1016/j.mmcr.2024.100647","url":null,"abstract":"<div><p>Fungal infections can be challenging to diagnose in returning travellers due to their non-specific clinical manifestations and changing epidemiology. We present a case of progressive disseminated histoplasmosis in a returning traveller from Bangladesh. The patient had a progressive and prolonged respiratory illness necessitating mechanical ventilatory support. The clue to potential fungal aetiology was provided by serum fungal markers - 1-3-β-D-glucan and <em>Aspergillus</em> galactomannan. Diagnosis was eventually made using panfungal PCR on bronchioalveolar lavage fluid.</p></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"44 ","pages":"Article 100647"},"PeriodicalIF":2.2,"publicationDate":"2024-04-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2211753924000216/pdfft?md5=2d8cae5c55e2d853fb3dae6a0dfeb21b&pid=1-s2.0-S2211753924000216-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140551711","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}
Pub Date : 2024-04-09DOI: 10.1016/j.mmcr.2024.100648
Marie Louise Aicher , Jeanne Bisch-Karatas , Alexander Maurer , Franca Wagner , Martin Wartenberg , Stefan Zimmerli
We describe a case of rhino-orbital-cerebral mucormycosis (ROCM) in a diabetic patient. She presented with cavernous sinus syndrome and ischemia of the optic nerve. Initially unremarkable findings in the nasal cavity and paranasal sinus delayed early diagnosis. Within two weeks, a follow-up MRI showing progressive orbital inflammation, thrombosis of the cavernous sinus and erosive destruction of the left middle nasal concha together with necrotic black tissue in the left nasal cavity and destruction of the maxillary sinus demonstrated in a consecutively performed ethmoidectomy, finally gave way to diagnosis. Definite diagnosis was established by histopathology and culture. Treatment consisted of a combination of liposomal Amphotericin B, partial surgical resection and improved diabetes control. Despite insufficient surgical treatment, the progression of the disease was remarkably slow – a typical hallmark of chronic ROCM.
With this case report we aim to underline the difficulties in establishing a prompt diagnosis of ROCM and to remind readers of its chronic form.
2012 Elsevier Ltd. All rights reserved.
我们描述了一例糖尿病患者的鼻-眶-脑粘液瘤病(ROCM)病例。她出现了海绵窦综合征和视神经缺血。最初鼻腔和副鼻窦的检查结果并不明显,因此延误了早期诊断。在两周内,随访的磁共振成像显示眶内炎症进展、海绵窦血栓形成、左中鼻孔侵蚀性破坏、左鼻腔坏死的黑色组织以及在连续进行的乙状窦切除术中显示的上颌窦破坏,最终为诊断提供了依据。通过组织病理学检查和培养,确定了确诊。治疗包括两性霉素 B 脂质体、部分手术切除和改善糖尿病控制。通过本病例报告,我们希望强调迅速诊断 ROCM 的困难,并提醒读者注意其慢性形式。2012 Elsevier Ltd. 保留所有权利。
{"title":"Rare case of a chronic rhinocerebral mucormycosis","authors":"Marie Louise Aicher , Jeanne Bisch-Karatas , Alexander Maurer , Franca Wagner , Martin Wartenberg , Stefan Zimmerli","doi":"10.1016/j.mmcr.2024.100648","DOIUrl":"https://doi.org/10.1016/j.mmcr.2024.100648","url":null,"abstract":"<div><p>We describe a case of rhino-orbital-cerebral mucormycosis (ROCM) in a diabetic patient. She presented with cavernous sinus syndrome and ischemia of the optic nerve. Initially unremarkable findings in the nasal cavity and paranasal sinus delayed early diagnosis. Within two weeks, a follow-up MRI showing progressive orbital inflammation, thrombosis of the cavernous sinus and erosive destruction of the left middle nasal concha together with necrotic black tissue in the left nasal cavity and destruction of the maxillary sinus demonstrated in a consecutively performed ethmoidectomy, finally gave way to diagnosis. Definite diagnosis was established by histopathology and culture. Treatment consisted of a combination of liposomal Amphotericin B, partial surgical resection and improved diabetes control. Despite insufficient surgical treatment, the progression of the disease was remarkably slow – a typical hallmark of chronic ROCM.</p><p>With this case report we aim to underline the difficulties in establishing a prompt diagnosis of ROCM and to remind readers of its chronic form.</p><p>2012 Elsevier Ltd. All rights reserved.</p></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"44 ","pages":"Article 100648"},"PeriodicalIF":2.2,"publicationDate":"2024-04-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2211753924000228/pdfft?md5=010625ca07f772f5df28f39267781908&pid=1-s2.0-S2211753924000228-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140552687","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}
Pub Date : 2024-04-04DOI: 10.1016/j.mmcr.2024.100645
Olga S. Tatarinova , Caroline L. Furness , Andrew M. Borman , Joy Barber , Nagarajan Muthialu , Laura Ferreras-Antolin
Neosartorya udagawae is a known cause of fungal infection in humans and animals. It is found to be more refractory to antifungal treatment in comparison to other Aspergillus species. With this report we present a case of proven invasive infection with Neosartorya udagawae in a child with chronic myeloid leukaemia after haematopoietic stem cell transplant. The patient received several lines of antifungal therapy including dual therapy appropriate to the antifungal susceptibility profile with progression of the invasive fungal disease requiring left lung upper lobe lobectomy. The case emphasizes the importance of early biopsy with antifungal susceptibility testing for targeted therapy and demonstrates the potential requirement for surgical management in addition to appropriate antifungal treatment.
{"title":"Neosartorya udagawae pulmonary infection requiring a surgical treatment in a paediatric haematopoietic progenitor cell recipient","authors":"Olga S. Tatarinova , Caroline L. Furness , Andrew M. Borman , Joy Barber , Nagarajan Muthialu , Laura Ferreras-Antolin","doi":"10.1016/j.mmcr.2024.100645","DOIUrl":"https://doi.org/10.1016/j.mmcr.2024.100645","url":null,"abstract":"<div><p><em>Neosartorya udagawae</em> is a known cause of fungal infection in humans and animals. It is found to be more refractory to antifungal treatment in comparison to other <em>Aspergillus</em> species. With this report we present a case of proven invasive infection with <em>Neosartorya udagawae</em> in a child with chronic myeloid leukaemia after haematopoietic stem cell transplant. The patient received several lines of antifungal therapy including dual therapy appropriate to the antifungal susceptibility profile with progression of the invasive fungal disease requiring left lung upper lobe lobectomy. The case emphasizes the importance of early biopsy with antifungal susceptibility testing for targeted therapy and demonstrates the potential requirement for surgical management in addition to appropriate antifungal treatment.</p></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"44 ","pages":"Article 100645"},"PeriodicalIF":2.2,"publicationDate":"2024-04-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2211753924000198/pdfft?md5=01f8bef143761a16b40d0a7ee107627d&pid=1-s2.0-S2211753924000198-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140535590","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}
Pub Date : 2024-04-02DOI: 10.1016/j.mmcr.2024.100646
Nakul Dar , Abigail Wills , Scott Berg , Sarah E. Gradecki , Thomas G. Cropley , Darren Guffey
Mucormycosis is a frequently lethal fungal infection that most commonly affects patients with poorly controlled diabetes or other immunosuppressed states. We report the case of a suspected disseminated Rhizopus infection in a patient who was pursuing naturopathic treatment including mud baths for metastatic adrenocortical carcinoma. He was empirically treated with liposomal amphotericin B but opted to stop treatment following multiorgan failure. The patient passed away on the tenth day of his hospital admission.
粘孢子菌病是一种常见的致命真菌感染,最常见于糖尿病或其他免疫抑制状态控制不佳的患者。我们报告了一例疑似根霉菌播散性感染的病例,患者因转移性肾上腺皮质癌接受自然疗法,包括泥浴治疗。他曾接受脂质体两性霉素 B 的经验性治疗,但在多器官功能衰竭后选择停止治疗。患者在入院第十天去世。
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