Haemophagocytic lymphohistiocytosis secondary to Histoplasma infection is rare and almost always occurs in immunocompromised hosts. We report a 32-year-old immunocompetent man presenting with a nonspecific febrile illness found to have disseminated histoplasmosis and associated haemophagocytic lymphohistiocytosis. The diagnosis was confirmed on histopathological examination and PCR of liver and bone marrow biopsies. He was successfully treated with steroids, intravenous immunoglobulin and itraconazole.
{"title":"Haemophagocytic lymphohistiocytosis secondary to disseminated histoplasmosis in an immunocompetent patient","authors":"Mallory Morton , Vinay Vanguru , Joo-Shik Shin , Amrita Ronnachit","doi":"10.1016/j.mmcr.2024.100635","DOIUrl":"https://doi.org/10.1016/j.mmcr.2024.100635","url":null,"abstract":"<div><p>Haemophagocytic lymphohistiocytosis secondary to <em>Histoplasma</em> infection is rare and almost always occurs in immunocompromised hosts. We report a 32-year-old immunocompetent man presenting with a nonspecific febrile illness found to have disseminated histoplasmosis and associated haemophagocytic lymphohistiocytosis. The diagnosis was confirmed on histopathological examination and PCR of liver and bone marrow biopsies. He was successfully treated with steroids, intravenous immunoglobulin and itraconazole.</p></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"43 ","pages":"Article 100635"},"PeriodicalIF":2.2,"publicationDate":"2024-02-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2211753924000095/pdfft?md5=fa483becfeccbcdb38767fa88aada861&pid=1-s2.0-S2211753924000095-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139941679","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 : 2024-02-16DOI: 10.1016/j.mmcr.2024.100634
Nayla Azanki Hatem , Alessandro C. Pasqualotto , Cecília Bittencourt Severo , Rafael Hannaui Bastos , Rafael de Luca de Lucena , Cezar Vinícius Würdig Riche
A 37-year-old immunocompetent man was admitted to the emergency department due to recurrent pain and oedema of his right knee. Two months earlier, he had undergone surgery to repair his meniscus. Arthroscopic joint lavage was performed and Candida dubliniensis was recovered in culture. The authors describe the first case of septic arthritis caused by Candida dubliniensis.
{"title":"Septic arthritis caused by Candida dubliniensis following arthroscopic surgery","authors":"Nayla Azanki Hatem , Alessandro C. Pasqualotto , Cecília Bittencourt Severo , Rafael Hannaui Bastos , Rafael de Luca de Lucena , Cezar Vinícius Würdig Riche","doi":"10.1016/j.mmcr.2024.100634","DOIUrl":"https://doi.org/10.1016/j.mmcr.2024.100634","url":null,"abstract":"<div><p>A 37-year-old immunocompetent man was admitted to the emergency department due to recurrent pain and oedema of his right knee. Two months earlier, he had undergone surgery to repair his meniscus. Arthroscopic joint lavage was performed and <em>Candida dubliniensis</em> was recovered in culture. The authors describe the first case of septic arthritis caused by <em>Candida dubliniensis</em>.</p></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"43 ","pages":"Article 100634"},"PeriodicalIF":2.2,"publicationDate":"2024-02-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2211753924000083/pdfft?md5=d88caddd8014e8308e78e612f3e1a892&pid=1-s2.0-S2211753924000083-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139908468","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 : 2024-02-16DOI: 10.1016/j.mmcr.2024.100633
Norma B. Fernandez , Bram Spruijtenburg , Iris N. Tiraboschi , Jacques F. Meis , Ana Lugo , María Cecilia López Joffre , Eelco F.J. Meijer
Sporothrix brasiliensis is considered a highly virulent emerging pathogen that causes sporotrichosis in humans, mainly after zoonotic transmission from infected cats. The epidemic of this zoonosis that originated from Brazil has spread in the last decades, generating hyperendemic regions in Latin America. We present two cases of human sporotrichosis causes by S. brasiliensis in Buenos Aires, Argentina, with good clinical response to differing treatments after contact with sick cats. Using Short tandem repeat (STR) genotyping, the two S. brasiliensis cases appear to be introduced from Brazil and likely originate from the same source.
巴西孢子丝菌(Sporothrix brasiliensis)被认为是一种毒性很强的新病原体,主要通过受感染的猫进行人畜共患病传播,导致人类患上孢子丝菌病。这种源于巴西的人畜共患传染病在过去几十年中不断蔓延,在拉丁美洲形成了高流行区。我们在阿根廷布宜诺斯艾利斯发现了两例由巴西猫孢子丝菌引起的人类孢子丝菌病病例,患者在接触病猫后对不同的治疗方法临床反应良好。通过短串联重复序列(STR)基因分型,这两例 S. brasiliensis 似乎是从巴西引入的,很可能来自同一来源。
{"title":"Genotyping and clonal origin of Sporothrix brasiliensis in human sporotrichosis cases in Argentina","authors":"Norma B. Fernandez , Bram Spruijtenburg , Iris N. Tiraboschi , Jacques F. Meis , Ana Lugo , María Cecilia López Joffre , Eelco F.J. Meijer","doi":"10.1016/j.mmcr.2024.100633","DOIUrl":"https://doi.org/10.1016/j.mmcr.2024.100633","url":null,"abstract":"<div><p><em>Sporothrix brasiliensis</em> is considered a highly virulent emerging pathogen that causes sporotrichosis in humans, mainly after zoonotic transmission from infected cats. The epidemic of this zoonosis that originated from Brazil has spread in the last decades, generating hyperendemic regions in Latin America. We present two cases of human sporotrichosis causes by <em>S. brasiliensis</em> in Buenos Aires, Argentina, with good clinical response to differing treatments after contact with sick cats. Using Short tandem repeat (STR) genotyping, the two <em>S. brasiliensis</em> cases appear to be introduced from Brazil and likely originate from the same source.</p></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"43 ","pages":"Article 100633"},"PeriodicalIF":2.2,"publicationDate":"2024-02-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2211753924000071/pdfft?md5=9b9dc75c7eb7ee8becadf652f81e04a6&pid=1-s2.0-S2211753924000071-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139936749","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 : 2024-02-01DOI: 10.1016/j.mmcr.2024.100629
Robab Ebrahimibarogh , Mona Ghazanfari , Tahereh Shokohi , Ensieh Yousefiabdolmaleki , Amir Seyedmousavi , Mohammad T. Hedayati
Tinea capitis is a chronic fungal infection of the scalp occurring commonly in children of school age, especially in developing countries. It is caused primarily by the dermatophyte members of genera Microsporum and Trichophyton. Here we report presence of free-living mycelial stage of dermatophytes, a stage of fungal growth which form in culture medias, around affected hairs and skin scrapings of scalp lesions in a 3-year-old boy presenting with alopecia and multiple scaly, non-erythematous plaques. On direct microscopy examination using 10 % potassium hydroxide, the fungal hyphae and arthrospores were detected in ectothrix form. In addition, we also observed numerous multicellular, thick-walled spindle-shaped macroconidia around hairs and skin scrapings. To our knowledge this is the first study reporting dermatophyte's macroconidia directly seen on clinical samples. Species level identification of the dermatophyte isolate growing on Mycosel™ agar was confirmed by PCR-sequencing of internal transcribed spacer of ribosomal RNA as Microsporum ferrugineum. The patient was successfully treated with systemic itraconazole combined with topical ketoconazole shampoo.
{"title":"Tinea capitis due to Microsporum ferrugineum: A case of unusual laboratory finding on direct microscopic examination of infected hairs and skin lesions","authors":"Robab Ebrahimibarogh , Mona Ghazanfari , Tahereh Shokohi , Ensieh Yousefiabdolmaleki , Amir Seyedmousavi , Mohammad T. Hedayati","doi":"10.1016/j.mmcr.2024.100629","DOIUrl":"https://doi.org/10.1016/j.mmcr.2024.100629","url":null,"abstract":"<div><p>Tinea capitis is a chronic fungal infection of the scalp occurring commonly in children of school age, especially in developing countries. It is caused primarily by the dermatophyte members of genera <em>Microsporum</em> and <em>Trichophyton</em>. Here we report presence of free-living mycelial stage of dermatophytes, a stage of fungal growth which form in culture medias, around affected hairs and skin scrapings of scalp lesions in a 3-year-old boy presenting with alopecia and multiple scaly, non-erythematous plaques. On direct microscopy examination using 10 % potassium hydroxide, the fungal hyphae and arthrospores were detected in ectothrix form. In addition, we also observed numerous multicellular, thick-walled spindle-shaped macroconidia around hairs and skin scrapings. To our knowledge this is the first study reporting dermatophyte's macroconidia directly seen on clinical samples. Species level identification of the dermatophyte isolate growing on Mycosel™ agar was confirmed by PCR-sequencing of internal transcribed spacer of ribosomal RNA as <em>Microsporum ferrugineum.</em> The patient was successfully treated with systemic itraconazole combined with topical ketoconazole shampoo.</p></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"43 ","pages":"Article 100629"},"PeriodicalIF":2.2,"publicationDate":"2024-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2211753924000034/pdfft?md5=80b983de33d7ba9ce034beac2ea401c5&pid=1-s2.0-S2211753924000034-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139718572","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 report a case of a 20-year-old young woman with a large stucco keratosis in the mons veneris, one of the clinical variants of Seborrheic keratoses (SKs). Periodic acid-Schiff staining revealed a large number of Malassezia spores in the stratum corneum. After oral antifungal treatment with itraconazole for 4 weeks, the benign tumor was completely cleared without residue or recurrence, which may open a new perspective for exploring the pathogenesis of SKs.
{"title":"Malassezia infection associated with stucco keratosis","authors":"Zhan Zhou , Jiali Zhu , Bin Jiao , Songgan Jia , Yanping Jiang","doi":"10.1016/j.mmcr.2024.100630","DOIUrl":"https://doi.org/10.1016/j.mmcr.2024.100630","url":null,"abstract":"<div><p>We report a case of a 20-year-old young woman with a large stucco keratosis in the mons veneris, one of the clinical variants of Seborrheic keratoses (SKs). Periodic acid-Schiff staining revealed a large number of <em>Malassezia</em> spores in the stratum corneum. After oral antifungal treatment with itraconazole for 4 weeks, the benign tumor was completely cleared without residue or recurrence, which may open a new perspective for exploring the pathogenesis of SKs.</p></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"43 ","pages":"Article 100630"},"PeriodicalIF":2.2,"publicationDate":"2024-01-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2211753924000046/pdfft?md5=ffa78a443013fa62817ec77b44b48e3c&pid=1-s2.0-S2211753924000046-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139654187","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 : 2024-01-24DOI: 10.1016/j.mmcr.2024.100631
Syed Nabil , Mohd Ferdaus Isa , Badrul Iskandar Abdul Wahab , Nurismah Md Isa
Sporotrichosis is a rare type of fungal infection caused by Sporothrix fungus. Transmissions are commonly by traumatic inoculation of the fungus through the skin and subcutaneous tissue either from environmental exposure or contact with infected animals. Due to its mode of transmission, it is commonly affecting the upper limbs. Definitive diagnosis can be obtained by fungal culture test on secretion fluids, pus, bloods or tissue biopsy. We report a rare presentation of this disease appearing as a solitary chronic ulcer of the lip which was successfully treated with itraconazole.
{"title":"Oral mucosa sporotrichosis: Report of a rare case acquired by direct inoculation","authors":"Syed Nabil , Mohd Ferdaus Isa , Badrul Iskandar Abdul Wahab , Nurismah Md Isa","doi":"10.1016/j.mmcr.2024.100631","DOIUrl":"10.1016/j.mmcr.2024.100631","url":null,"abstract":"<div><p>Sporotrichosis is a rare type of fungal infection caused by <em>Sporothrix</em> fungus. Transmissions are commonly by traumatic inoculation of the fungus through the skin and subcutaneous tissue either from environmental exposure or contact with infected animals. Due to its mode of transmission, it is commonly affecting the upper limbs. Definitive diagnosis can be obtained by fungal culture test on secretion fluids, pus, bloods or tissue biopsy. We report a rare presentation of this disease appearing as a solitary chronic ulcer of the lip which was successfully treated with itraconazole.</p></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"43 ","pages":"Article 100631"},"PeriodicalIF":2.2,"publicationDate":"2024-01-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2211753924000058/pdfft?md5=a97630fd0f2cf32e22f56e4fa393555c&pid=1-s2.0-S2211753924000058-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139638982","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 : 2024-01-22DOI: 10.1016/j.mmcr.2024.100628
Yasser Al-Ghabra , Mohammad Hamdi , Ahmad Alkheder , Ahmad Kammasha , Shams Shamso , Adham Bader Aldeen Mohsen
A 2-month-old Syrian male child presented with a large blackish ulcerating lesion on his hard palate, along with fever, diarrhea, vomiting, and milk regurgitation from the nose. The child was diagnosed with palatal mucormycosis by histopathology and underwent treatment with liposomal amphotericin B and surgical debridement. However, despite treatment, the child's condition deteriorated, and he died from respiratory failure. An underlying immunodeficiency was not diagnosed, but the family history revealed several deaths of the child's siblings at very early ages due to poorly documented complicated metabolic syndromes. An autopsy was refused by the parents due to cultural reasons.
一名2个月大的叙利亚男童因硬腭上出现大面积黑色溃疡,伴有发烧、腹泻、呕吐和鼻腔反流牛奶而就诊。经组织病理学检查,该患儿被诊断为腭粘液瘤病,并接受了两性霉素 B 脂质体治疗和手术清创。然而,尽管进行了治疗,孩子的病情还是恶化了,最后死于呼吸衰竭。虽然没有诊断出潜在的免疫缺陷,但家族病史显示,该患儿的几个兄弟姐妹在很小的时候就因复杂的代谢综合征而死亡。由于文化原因,父母拒绝进行尸检。
{"title":"Palatal mucormycosis in a 2-month-old child: A very rare case report and a literature review","authors":"Yasser Al-Ghabra , Mohammad Hamdi , Ahmad Alkheder , Ahmad Kammasha , Shams Shamso , Adham Bader Aldeen Mohsen","doi":"10.1016/j.mmcr.2024.100628","DOIUrl":"10.1016/j.mmcr.2024.100628","url":null,"abstract":"<div><p>A 2-month-old Syrian male child presented with a large blackish ulcerating lesion on his hard palate, along with fever, diarrhea, vomiting, and milk regurgitation from the nose. The child was diagnosed with palatal mucormycosis by histopathology and underwent treatment with liposomal amphotericin B and surgical debridement. However, despite treatment, the child's condition deteriorated, and he died from respiratory failure. An underlying immunodeficiency was not diagnosed, but the family history revealed several deaths of the child's siblings at very early ages due to poorly documented complicated metabolic syndromes. An autopsy was refused by the parents due to cultural reasons.</p></div>","PeriodicalId":51724,"journal":{"name":"Medical Mycology Case Reports","volume":"43 ","pages":"Article 100628"},"PeriodicalIF":2.2,"publicationDate":"2024-01-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2211753924000022/pdfft?md5=4df4570033271019c97490a871754653&pid=1-s2.0-S2211753924000022-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139638681","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 : 2024-01-14DOI: 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}