Medical Mycology Case Reports医学真菌学病例报告
Medical Mycology Case Reports(英文缩写 MED MYCOL CASE REP),ISSN 2211-7539,eISSN 2211-7539,中文译名:医学真菌学病例报告 是一本学术期刊。本页汇总该期刊的最新影响因子、分区信息以及最新收录于 PubMed 的文献,帮助您快速了解期刊全貌。
发文量统计区间：2025-10-01 至 2026-09-30，按本站收录文献的发表日期统计。
期刊介绍
历年影响因子趋势
| JCR 数据年份 | 影响因子 | JCR 分区 |
|---|---|---|
| 2021 | 未收录 | N/A |
| 2022 | 2.200 | N/A |
| 2023 | 1.600 | Q3 |
| 2024 | 1.300 | Q4 |
| 2025 | 1.100 | Q4 |
Medical Mycology Case Reports 最新收录文献
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1. {"_":" fungemia: A series of four cases.","i":["Rhodotorula"]}
PMID:日期:2026-09-18In immunocompromised patients, particularly those with indwelling central venous catheters or hematological disorders, . is increasingly implicated in nosocomial infections. We report a series of four cases of Fungemia. Two cases involved in adult patients from the intensive care unit with neurological conditions, while the other were pediatric patients with hematological diseases. . was identified. In vitro antifungal susceptibility testing revealed that fluconazole, voriconazole, and caspofungin exhibited intermediate to complete resistance.
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2. {"_":"From misdiagnosis to precision management: Thoracic vertebral infection caused by diagnosed using a multi-platform approach - A case report and literature review.","i":["Scedosporium boydii"]}
PMID:日期:2026-09-15spinal infection is rare and often mimics tuberculosis. We report a 54-year-old immunocompetent man with post-traumatic thoracic vertebral infection initially misdiagnosed as spinal tuberculosis. A multi-platform approach combining culture, matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS), and targeted next-generation sequencing (tNGS) identified . Surgical debridement and voriconazole resulted in complete recovery. A high index of suspicion and integrated diagnostics are essential to avoid mismanagement.
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3. {"_":"Case report of a brain abscess due to species complex in a renal transplanted patient.","i":["Nannizziopsis obscura"]}
PMID:日期:2026-09-04We here describe the case of a kidney transplant patient from Mali who presented with multiple complex seizures followed by a facial paresis revealing a brain abscess due to species complex. This fungal species is usually implicated in reptile skin infections and rarely disseminated infections. Very rarely, it can infect human beings suffering from immunodepression, causing various kinds of complications ranging from soft tissue abscesses to solid organ abscesses. This case highlights the potential wide range of pathogens involved and underlines the need for greater vigilance in the diagnosis and management of atypical infections in transplant settings.
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4. {"_":"First case report of onychomycosis caused by .","i":["Exophiala alcalophila"]}
4. {"_":"由","i":["Exophiala alcalophila"]} 引起的甲真菌病首例病例报告PMID:日期:2026-09-03A 46-year-old woman from Colombia, without any medical comorbidities, presented with marked yellowish discoloration of both big toenails, suggestive of onychomycosis, and malalignment of the nail plate. Culture of nail scrapings grew dark-pigmented, mucoid, yeast-like colonies identified as by ITS sequencing. Broth microdilution identified the isolate as resistant to fluconazole and the echinocandins. The patient refused antifungal treatment. This case highlights the importance of black yeast-like fungi as etiological agents of onychomycosis.
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5. Cutaneous mucormycosis in a patient with Hailey-Hailey disease (benign familial pemphigus) - first reported case.
PMID:日期:2026-08-31This report describes a case of primary cutaneous mucormycosis in a patient with Hailey-Hailey Disease (benign familial pemphigus). The diagnosis of primary cutaneous mucormycosis was confirmed via microbiological culture as well as histopathology. Our patient improved with prompt surgical debridement and excision of infected, necrotic tissue with complementary antifungal therapy. To the best of our knowledge this is the first reported case of cutaneous mucormycosis in a patient with Hailey-Hailey Disease and contributes to the literature regarding pathophysiology, management and treatment for each of these rare entities.
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6. Man-in-the-barrel syndrome caused by cervical arachnoiditis in refractory coccidioidal meningitis.
PMID:日期:2026-08-24We report a case of refractory coccidioidal meningitis presenting with bilateral upper-extremity weakness in a man-in-a-barrel distribution caused by cervical arachnoiditis, adhesive bands, and spinal cord compression. The patient was treated sequentially with fluconazole, other azole therapy, liposomal amphotericin B, intrathecal amphotericin B, and olorofim, with only partial disease control. Neuroimaging demonstrated progressive cervical leptomeningeal inflammation, cord tethering, and CT myelography illustrated adhesive arachnoiditis. Surgical lysis of adhesions and placement of a spinal Ommaya reservoir for intrathecal amphotericin delivery above and below the obstructed segment resulted in partial neurologic improvement. This case broadens the differential diagnosis of man-in-a-barrel syndrome to include active fungal meningitis with compressive cervical myelopathy and highlights the role of combined surgical-medical management in complicated fungal arachnoiditis.
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7. {"_":"Double zoonosis: Parinaud oculoglandular syndrome from sporotrichosis and follicular conjunctivitis from , a zoonotic co-infection from our feline friend.","i":["Moraxella osloensis"]}
PMID:日期:2026-08-21A 41-year-old woman developed chronic unilateral granulomatous conjunctivitis, ipsilateral lymphadenopathy, fever and malaise, diagnostic of Parinaud oculoglandular syndrome, after contact with a sick pet cat. Tear cultures identified , confirmed by 18S ribosomal RNA PCR, with co-infection by . Biopsy showed suppurative necrotising granulomatous inflammation. Oral itraconazole, topical amphotericin B and amikacin achieved remission. Although is the commonest cause of POGS, warrants consideration in cat-exposed patients, alongside bacterial co-infection.
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8. {"_":"Onychomycosis caused by species in a patient with Crohn's Disease in Iraq: A case report.","i":["Syncephalastrum"]}
PMID:日期:2026-08-17Onychomycosis is one of the most common nail disorders worldwide and is predominantly caused by dermatophytes; however, infections caused by non-dermatophyte molds are increasingly recognized as important causes of nail disease. We present a case of a 41-year-old male from Duhok, Iraq, with a 15-year history of Crohn's Disease. He presented with progressive discoloration, nail thickening, nail deformity, pain while walking and brittleness of the affected nail that had persisted for several months. He was diagnosed with onychomycosis due to species confirmed by KOH microscopy and characteristic culture morphology. Molecular confirmation was not available to identify to the species level. The fungus was sensitive to itraconazole, nystatin, clotrimazole, amphotericin B, miconazole, and ketoconazole, but showed resistance to fluconazole and voriconazole. He was successfully treated using IV amphotericin B, topical clotrimazole, and nail surgery. This case demonstrates that species can cause clinically significant onychomycosis and should not automatically be dismissed as laboratory contaminants. A combination of clinical assessment, direct microscopy, culture-based identification, and antifungal susceptibility testing is essential for establishing diagnosis and guiding appropriate management.
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9. Invasive pulmonary aspergillosis following mild Covid-19 in an autologous hematopoietic stem cell transplant recipient: A case report.
PMID:日期:2026-08-03COVID-19-associated pulmonary aspergillosis (CAPA) is typically described in critically ill patients with severe pneumonia. We report a 68-year-old man, 16 weeks post autologous hematopoietic stem cell transplant for AL amyloidosis, who developed invasive pulmonary aspergillosis (IPA) following mild COVID-19 upper respiratory tract infection not requiring oxygen supplementation or ICU admission. Diagnosis was established by positive broncho-alveolar lavage galactomannan with compatible CT chest findings, and he was treated with oral voriconazole. This case highlights that IPA may complicate mild COVID-19 in patients not traditionally considered at highest risk, supporting the concept that cumulative risk factors may precipitate IPA.
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10. {"_":"First report of osteomyelitis with CNS dissemination in a pediatric CGD patient post-HSCT: A case report and literature review.","i":["Rhinocladiella mackenziei"]}
PMID:日期:2026-08-03is a rare neurotropic dematiaceous fungus that causes cerebral phaeohyphomycosis, predominantly in immunocompetent adults with a geographical predilection to the Middle East. Pediatric infection is exceptionally rare, and to our knowledge, no cases of combined osseous and central nervous system involvement following hematopoietic stem cell transplantation (HSCT) have been reported. We report a male child with autosomal recessive chronic granulomatous disease (CGD) who developed traumatic forearm osteomyelitis due to several months after haploidentical HSCT. Subsequent neuroimaging demonstrated intracerebral abscesses despite immune reconstitution. The infection persisted despite prolonged combination antifungal therapy with voriconazole and amphotericin B and ultimately required neurosurgical excision. The patient recovered without neurological sequelae and continues on long-term posaconazole therapy. This case highlights as a cause of severe, invasive, disseminated fungal disease in pediatric post-bone marrow transplant patients and demonstrates extracerebral inoculation with subsequent CNS dissemination. It also underscores the importance of early recognition and a combined medical-surgical approach in management of refractory disease.