Pub Date : 2024-01-14DOI: 10.1016/j.mmcr.2024.100627
Mário Pinto, João Rodrigues, Marta Silva, Dionísio Maia, António Miguel
A 37-year-old man presented with chronic cavitary pulmonary aspergillosis and hemoptysis refractory to systemic antifungal therapy with voriconazole and bronchial artery embolization. Surgical excision was unfeasible due to the patient's refusal of blood transfusions. Ten sessions of intracavitary instillation of amphotericin B via flexible bronchoscopy were then performed. Hemoptysis cessation and aspergilloma resolution were achieved, with no toxicity or side effects, and the clinical benefits were sustained at six months of follow-up.
一名 37 岁的男子因慢性腔隙性肺曲霉病和咯血而就诊,使用伏立康唑全身抗真菌治疗和支气管动脉栓塞治疗均无效。由于患者拒绝输血,手术切除不可行。随后,通过柔性支气管镜进行了十次两性霉素 B 腔内灌注。患者咯血停止,曲霉瘤消退,没有出现任何毒副作用。
{"title":"Endobronchial amphotericin B to treat hemoptysis in an inoperable patient with aspergillosis","authors":"Mário Pinto, João Rodrigues, Marta Silva, Dionísio Maia, António Miguel","doi":"10.1016/j.mmcr.2024.100627","DOIUrl":"https://doi.org/10.1016/j.mmcr.2024.100627","url":null,"abstract":"<div><p>A 37-year-old man presented with chronic cavitary pulmonary aspergillosis and hemoptysis refractory to systemic antifungal therapy with voriconazole and bronchial artery embolization. Surgical excision was unfeasible due to the patient's refusal of blood transfusions. Ten sessions of intracavitary instillation of amphotericin B via flexible bronchoscopy were then performed. Hemoptysis cessation and aspergilloma resolution were achieved, with no toxicity or side effects, and the clinical benefits were sustained at six months of follow-up.</p></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"43 ","pages":"Article 100627"},"PeriodicalIF":2.2,"publicationDate":"2024-01-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2211753924000010/pdfft?md5=4ff2508192a1e1e69000e7dccd698270&pid=1-s2.0-S2211753924000010-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139493414","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}
Sporotrichosis is an implantation mycosis due to the genus Sporothrix. Cutaneous disseminated sporotrichosis is an unusual clinical form that often affects immunocompromised patients. We report a case of cutaneous disseminated sporotrichosis in an immunocompetent famer from a rural region of Madagascar, treated successfully with Itraconazole 200mg twice a day. This case highlights the role of multiple inoculation affecting different parts of the body as a risk factor of cutaneous disseminated sporotrichosis in an immunocompetent individually.
{"title":"Cutaneous disseminated sporotrichosis in an immunocompetent farmer","authors":"Mendrika Fifaliana Rakotoarisaona , Malalaniaina Andrianarison , Fandresena Arilala Sendrasoa , Tahinamandranto Rasamoelina , Lala Soavina Ramarozatovo , Fahafahantsoa Rapelanoro Rabenja","doi":"10.1016/j.mmcr.2023.100626","DOIUrl":"10.1016/j.mmcr.2023.100626","url":null,"abstract":"<div><p>Sporotrichosis is an implantation mycosis due to the genus <em>Sporothrix</em>. Cutaneous disseminated sporotrichosis is an unusual clinical form that often affects immunocompromised patients. We report a case of cutaneous disseminated sporotrichosis in an immunocompetent famer from a rural region of Madagascar, treated successfully with Itraconazole 200mg twice a day. This case highlights the role of multiple inoculation affecting different parts of the body as a risk factor of cutaneous disseminated sporotrichosis in an immunocompetent individually.</p></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"43 ","pages":"Article 100626"},"PeriodicalIF":2.2,"publicationDate":"2024-01-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2211753923000581/pdfft?md5=2da75f21a1b1cac8e0334b86b318617e&pid=1-s2.0-S2211753923000581-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139395544","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 : 2023-12-30DOI: 10.1016/j.mmcr.2023.100623
Koos Korsten , Josje Altenburg , Marieke Gittelbauer , Peter van Hengel , Rogier Jansen , Karin van Dijk
After having traveled to California in 2017, a 26-year old Dutch man presented in 2020 with persisting cough and shortness of breath. Radiology showed cystic bronchiectasis with peri-bronchial consolidation in his right upper lobe. Laboratory studies in August 2021 showed an increased total IgE, specific Aspergillus IgE, eosinophilia and positive BAL culture for Coccidioides immitis/posadasii. After 6 weeks of itraconazole treatment for suspected allergic bronchopulmonary aspergillosis, symptoms persisted and respiratory cultures remained positive. The infection was cleared after a 6-month course of fluconazole. (max 75 words)
{"title":"Coccidioidomycosis presenting years after returning from travel","authors":"Koos Korsten , Josje Altenburg , Marieke Gittelbauer , Peter van Hengel , Rogier Jansen , Karin van Dijk","doi":"10.1016/j.mmcr.2023.100623","DOIUrl":"https://doi.org/10.1016/j.mmcr.2023.100623","url":null,"abstract":"<div><p>After having traveled to California in 2017, a 26-year old Dutch man presented in 2020 with persisting cough and shortness of breath. Radiology showed cystic bronchiectasis with peri-bronchial consolidation in his right upper lobe. Laboratory studies in August 2021 showed an increased total IgE, specific <em>Aspergillus</em> IgE, eosinophilia and positive BAL culture for <em>Coccidioides immitis/posadasii</em>. After 6 weeks of itraconazole treatment for suspected allergic bronchopulmonary aspergillosis, symptoms persisted and respiratory cultures remained positive. The infection was cleared after a 6-month course of fluconazole. (max 75 words)</p></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"43 ","pages":"Article 100623"},"PeriodicalIF":2.2,"publicationDate":"2023-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2211753923000556/pdfft?md5=18e8eb0e089e170da7d4c2a488a22e92&pid=1-s2.0-S2211753923000556-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139108672","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}
Herein, we report a case of pancreatic cancer with acute cholangitis secondary to biliary obstruction. Empirical antibiotic therapy did not change the clinical presentation. Blood cultures were sterile; however, bile culture was positive for yeasts. Our laboratory analysis revealed a biliary coinfection by multidrug-resistant C. glabrata and C. albicans. The patient was successfully treated with endoscopic biliary drainage.
{"title":"Biliary co-infection by multidrug-resistant Candida glabrata and Candida albicans in a case of pancreatic cancer with cholangitis: A case report and review of literature","authors":"Amir Sadeghi , Hamidreza Houri , Ensieh Lotfali , Erfan Ghadirzadeh , Mohsen Rajabnia","doi":"10.1016/j.mmcr.2023.100625","DOIUrl":"10.1016/j.mmcr.2023.100625","url":null,"abstract":"<div><p>Herein, we report a case of pancreatic cancer with acute cholangitis secondary to biliary obstruction. Empirical antibiotic therapy did not change the clinical presentation. Blood cultures were sterile; however, bile culture was positive for yeasts. Our laboratory analysis revealed a biliary coinfection by multidrug-resistant C. glabrata and C. albicans. The patient was successfully treated with endoscopic biliary drainage.</p></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"43 ","pages":"Article 100625"},"PeriodicalIF":2.2,"publicationDate":"2023-12-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S221175392300057X/pdfft?md5=aa19dd081466b0884c7b56dbbe9dff2a&pid=1-s2.0-S221175392300057X-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139189572","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 : 2023-12-26DOI: 10.1016/j.mmcr.2023.100624
María Carolina Escobar , Federico Cifuentes Ramos , Cristian A. Alvarez Rojas
We report Sporothrix brasiliensis infection in three cats from Santiago, Chile. Recently, S. brasiliensis was reported in cats from the southernmost region of Chile located 2,190 km from Santiago. Our findings emphasize the emergence of S. brasiliensis in the Chilean context, reflecting its rapid expansion across South America in recent years. Veterinarians should include S. brasiliensis in the differential diagnosis of skin conditions in cats.
{"title":"Sporothrix brasiliensis in cats from Santiago, Chile","authors":"María Carolina Escobar , Federico Cifuentes Ramos , Cristian A. Alvarez Rojas","doi":"10.1016/j.mmcr.2023.100624","DOIUrl":"https://doi.org/10.1016/j.mmcr.2023.100624","url":null,"abstract":"<div><p>We report <em>Sporothrix brasiliensis</em> infection in three cats from Santiago, Chile. Recently, <em>S</em>. <em>brasiliensis</em> was reported in cats from the southernmost region of Chile located 2,190 km from Santiago. Our findings emphasize the emergence of <em>S</em>. <em>brasiliensis</em> in the Chilean context, reflecting its rapid expansion across South America in recent years. Veterinarians should include <em>S</em>. <em>brasiliensis</em> in the differential diagnosis of skin conditions in cats.</p></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"43 ","pages":"Article 100624"},"PeriodicalIF":2.2,"publicationDate":"2023-12-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2211753923000568/pdfft?md5=ac888775fb28ed20ae073534e7f6a669&pid=1-s2.0-S2211753923000568-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139100670","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 : 2023-12-24DOI: 10.1016/j.mmcr.2023.100622
Alexander Jimbo-Zapata , Gabriela Sevillano , Pilar Rodríguez , José Rubén Ramírez-Iglesias , Juan-Carlos Navarro
Filamentous fungal infections are an important cause of systemic infections in immunocompromised patients. Fusarium genus members potentially cause disseminated infections, especially in patients with catheters, due to the ability to adhere to these devices. We describe a case of fatal fungemia due to Fusarium oxysporum in a patient with COVID-19 in Ecuador. The genus identification was carried out with conventional techniques and species identification by molecular and phylogenetic techniques through sequencing of the ITS region.
丝状真菌感染是免疫力低下患者全身感染的重要原因。镰刀菌属的成员由于能够附着在导管上,因此有可能引起播散性感染,尤其是在使用导管的患者中。我们描述了厄瓜多尔一名 COVID-19 患者因镰刀菌引起的致命真菌血症病例。属的鉴定采用常规技术,种的鉴定采用分子和系统发育技术,通过对 ITS 区域进行测序。
{"title":"First report of fatal fungemia due Fusarium oxysporum in a patient with COVID-19 in Ecuador","authors":"Alexander Jimbo-Zapata , Gabriela Sevillano , Pilar Rodríguez , José Rubén Ramírez-Iglesias , Juan-Carlos Navarro","doi":"10.1016/j.mmcr.2023.100622","DOIUrl":"https://doi.org/10.1016/j.mmcr.2023.100622","url":null,"abstract":"<div><p>Filamentous fungal infections are an important cause of systemic infections in immunocompromised patients. <em>Fusarium</em> genus members potentially cause disseminated infections, especially in patients with catheters, due to the ability to adhere to these devices. We describe a case of fatal fungemia due to <em>Fusarium oxysporum</em> in a patient with COVID-19 in Ecuador. The genus identification was carried out with conventional techniques and species identification by molecular and phylogenetic techniques through sequencing of the ITS region.</p></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"43 ","pages":"Article 100622"},"PeriodicalIF":2.2,"publicationDate":"2023-12-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2211753923000544/pdfft?md5=81c9ce4156764cfc0e00a6041a976ebe&pid=1-s2.0-S2211753923000544-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139100669","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}
Muyocopron laterale is a type of endophytic fungus that parasitizes monocotyledonous plants. Cases of humans and other mammals being infected by M. laterale are very rare around the world. We report the first case of subcutaneous mycosis caused by M. laterale in China. A kidney transplant recipient was admitted for Pneumocystis carinii pneumonia and subsequently developed left calf redness and swelling due to a M. laterale infection. The patient was treated with sulfamethoxazole and voriconazole and underwent five surgical debridements and vacuum sealing drainage (VSD) applications with the left leg. The patient was eventually cured and discharged from the hospital.
{"title":"The first case of subcutaneous mycosis caused by Muyocopron laterale in China","authors":"Tingting Yang, Yikan Ding, Yajie Fu, Hongchao Chen","doi":"10.1016/j.mmcr.2023.100620","DOIUrl":"10.1016/j.mmcr.2023.100620","url":null,"abstract":"<div><p><em>Muyocopron laterale</em> is a type of endophytic fungus that parasitizes monocotyledonous plants. Cases of humans and other mammals being infected by <em>M. laterale</em> are very rare around the world. We report the first case of subcutaneous mycosis caused by <em>M. laterale</em> in China. A kidney transplant recipient was admitted for <em>Pneumocystis carinii</em> pneumonia and subsequently developed left calf redness and swelling due to a <em>M. laterale</em> infection. The patient was treated with sulfamethoxazole and voriconazole and underwent five surgical debridements and vacuum sealing drainage (VSD) applications with the left leg. The patient was eventually cured and discharged from the hospital.</p></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"43 ","pages":"Article 100620"},"PeriodicalIF":2.2,"publicationDate":"2023-12-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2211753923000520/pdfft?md5=70a7371b33f1a7e8ce35078d3c98078d&pid=1-s2.0-S2211753923000520-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139020644","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 : 2023-12-14DOI: 10.1016/j.mmcr.2023.100621
Hammad Ul Haq Qureshi , Muhammad Absar , Wafa Nasser , Mohamed Tahar Yacoubi
Cerebral phaeohyphomycosis (CP) is a serious form of phaeohyphomycosis. We report a case of CP caused by Fonsecaea species in a 66-year-old immunocompromised renal transplant recipient female. Craniotomy was performed on an irregularly enhancing right cerebellar hemisphere lesion and abscess and tissue samples collected for microbiological and histological evaluation, showing fungal elements and Fonsecaea species was isolated. Antifungal treatment with voriconazole & liposomal amphotericin B was initiated with a temporary improvement in the patient's condition. Deep vein thrombosis jeopardized patient's prognosis. Despite aggressive surgical and medical intervention, our patient succumbed to the disease. Historically, CP has been linked with fatality rates as high as 65 %, despite surgical intervention and systemic antifungal medication.
脑拟真菌病(CP)是拟真菌病的一种严重形式。我们报告了一例由丰塞卡菌引起的 CP 病例,患者是一名 66 岁的免疫功能低下的女性肾移植受者。我们对不规则强化的右侧小脑半球病灶进行了开颅手术,并采集脓肿和组织样本进行微生物学和组织学评估,结果显示有真菌成分,并分离出丰塞卡菌。开始使用伏立康唑和ampamp;两性霉素 B 脂质体进行抗真菌治疗,患者的病情暂时有所好转。深静脉血栓危及患者的预后。尽管采取了积极的手术和药物干预措施,但患者还是因病去世。从历史上看,尽管采取了手术干预和全身抗真菌药物治疗,CP 的致死率仍高达 65%。
{"title":"A rare case of cerebral phaeohyphomycosis caused by Fonsecaea species in a renal transplant patient","authors":"Hammad Ul Haq Qureshi , Muhammad Absar , Wafa Nasser , Mohamed Tahar Yacoubi","doi":"10.1016/j.mmcr.2023.100621","DOIUrl":"10.1016/j.mmcr.2023.100621","url":null,"abstract":"<div><p>Cerebral phaeohyphomycosis (CP) is a serious form of phaeohyphomycosis. We report a case of CP caused by <em>Fonsecaea</em> species in a 66-year-old immunocompromised renal transplant recipient female. Craniotomy was performed on an irregularly enhancing right cerebellar hemisphere lesion and abscess and tissue samples collected for microbiological and histological evaluation, showing fungal elements and <em>Fonsecaea</em> species was isolated. Antifungal treatment with voriconazole & liposomal amphotericin B was initiated with a temporary improvement in the patient's condition. Deep vein thrombosis jeopardized patient's prognosis. Despite aggressive surgical and medical intervention, our patient succumbed to the disease. Historically, CP has been linked with fatality rates as high as 65 %, despite surgical intervention and systemic antifungal medication.</p></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"43 ","pages":"Article 100621"},"PeriodicalIF":2.2,"publicationDate":"2023-12-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2211753923000532/pdfft?md5=23447b88c1d58221fbb8fcb787a625b9&pid=1-s2.0-S2211753923000532-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139017761","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}
Atypical fungal co-infections in post-COVID-19 patients may have been underreported due to limited diagnostic methods. We present a case of Chaetomium globosum sinusitis in a 55-year-old post-COVID-19 patient with pain in the left side of the face, mimicking rhino-cerebral mucormycosis.
CT-paranasal sinuses showed mucosal thickening of left paranasal sinuses, biopsy of which grew a velvety, white colony. It was confirmed as Chaetomium globosum. The patient responded to oral Posaconazole therapy for three months.
Prompt identification of atypical fungal agents is critical for appropriate treatment.
{"title":"Chaetomium globosum: Spotting a scarce saprophyte in bacterial-fungal co-infection of the sinuses in a post-COVID-19 patient","authors":"Neeta Gade , Soumyabrata Nag , Kiran Kumar Prathipati , Meena Mishra , Vishal Shete","doi":"10.1016/j.mmcr.2023.100618","DOIUrl":"https://doi.org/10.1016/j.mmcr.2023.100618","url":null,"abstract":"<div><p>Atypical fungal co-infections in post-COVID-19 patients may have been underreported due to limited diagnostic methods. We present a case of <em>Chaetomium globosum</em> sinusitis in a 55-year-old post-COVID-19 patient with pain in the left side of the face, mimicking rhino-cerebral mucormycosis.</p><p>CT-paranasal sinuses showed mucosal thickening of left paranasal sinuses, biopsy of which grew a velvety, white colony. It was confirmed as <em>Chaetomium globosum</em>. The patient responded to oral Posaconazole therapy for three months.</p><p>Prompt identification of atypical fungal agents is critical for appropriate treatment.</p></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"43 ","pages":"Article 100618"},"PeriodicalIF":2.2,"publicationDate":"2023-12-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2211753923000507/pdfft?md5=389a2fe5fb688e007de9ded8323e926b&pid=1-s2.0-S2211753923000507-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138559046","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 : 2023-11-13DOI: 10.1016/j.mmcr.2023.100615
Sergio Charles-Lozoya , Gibran Ruíz-Zenteno , María E. Lizcano-Martínez , Héctor Cobos-Aguilar , Joél León-Ruíz , Jesús Domínguez-Delgado
Surgical treatment of vertebral coccidioidomycosis presents a challenge, with an unpredictable course and uncertain results. We present a 52-year-old man with disseminated infection due to coccidioidomycosis in the thoracolumbar spine, with vertebral instability, and deferral surgical treatment due to SARS-CoV-2 contingency. Treatment with itraconazole was initiated, followed by liposomal amphotericin B and fluconazole due to a relapse. The patient was discharged long-term with voriconazole. The axial pain improved without neurological deficits. Surgical treatment was not required. 2012 Elsevier Ltd. All rights reserved.
{"title":"Vertebral coccidioidomycosis with mechanical instability treated solely with antifungals: A case report","authors":"Sergio Charles-Lozoya , Gibran Ruíz-Zenteno , María E. Lizcano-Martínez , Héctor Cobos-Aguilar , Joél León-Ruíz , Jesús Domínguez-Delgado","doi":"10.1016/j.mmcr.2023.100615","DOIUrl":"https://doi.org/10.1016/j.mmcr.2023.100615","url":null,"abstract":"<div><p>Surgical treatment of vertebral coccidioidomycosis presents a challenge, with an unpredictable course and uncertain results. We present a 52-year-old man with disseminated infection due to coccidioidomycosis in the thoracolumbar spine, with vertebral instability, and deferral surgical treatment due to SARS-CoV-2 contingency. Treatment with itraconazole was initiated, followed by liposomal amphotericin B and fluconazole due to a relapse. The patient was discharged long-term with voriconazole. The axial pain improved without neurological deficits. Surgical treatment was not required. 2012 Elsevier Ltd. All rights reserved.</p></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"42 ","pages":"Article 100615"},"PeriodicalIF":2.2,"publicationDate":"2023-11-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2211753923000477/pdfft?md5=3d11cc44d084849d4f7e592184ac3fb1&pid=1-s2.0-S2211753923000477-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"134831991","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}