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Fingolimod-associated cryptococcal meningitis in a patient with Multiple Sclerosis: A case report and literature review
IF 1.1
IDCases Pub Date : 2025-01-01 DOI: 10.1016/j.idcr.2025.e02150
Hidenori Nakagawa , Akari Takagi , Takahiro Mitsueda , Michinori Shirano
{"title":"Fingolimod-associated cryptococcal meningitis in a patient with Multiple Sclerosis: A case report and literature review","authors":"Hidenori Nakagawa ,&nbsp;Akari Takagi ,&nbsp;Takahiro Mitsueda ,&nbsp;Michinori Shirano","doi":"10.1016/j.idcr.2025.e02150","DOIUrl":"10.1016/j.idcr.2025.e02150","url":null,"abstract":"<div><div>A 65-year-old woman with Multiple Sclerosis treated with fingolimod developed headaches and convulsions. Cerebrospinal fluid (CSF) culture indicated <em>Cryptococcus neoformans</em>. A literature review of 20 cases of cryptococcal meningitis indicated that headache was the most common initial symptom, and all cases were positive for serum and/or CSF cryptococcal antigens.</div></div>","PeriodicalId":47045,"journal":{"name":"IDCases","volume":"39 ","pages":"Article e02150"},"PeriodicalIF":1.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11773199/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143061129","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
Coinfection of Herpes Simplex virus 2 and Mycobacterium chelonae in acute hydrops associated with keratoconus: A case report
IF 1.1
IDCases Pub Date : 2025-01-01 DOI: 10.1016/j.idcr.2025.e02176
Pedro Marques-Couto , Ana Gama-Castro , Teresa Carvalho , Rodrigo Vilares-Morgado , João Pinheiro-Costa , Dolores Pinheiro , Ana Maria Cunha
{"title":"Coinfection of Herpes Simplex virus 2 and Mycobacterium chelonae in acute hydrops associated with keratoconus: A case report","authors":"Pedro Marques-Couto ,&nbsp;Ana Gama-Castro ,&nbsp;Teresa Carvalho ,&nbsp;Rodrigo Vilares-Morgado ,&nbsp;João Pinheiro-Costa ,&nbsp;Dolores Pinheiro ,&nbsp;Ana Maria Cunha","doi":"10.1016/j.idcr.2025.e02176","DOIUrl":"10.1016/j.idcr.2025.e02176","url":null,"abstract":"<div><h3>Purpose</h3><div>Acute hydrops is a characteristic complication of corneal ectatic diseases. While <em>Mycobacterium chelonae</em> is known to cause various ophthalmic infections, most commonly following surgery, there are no reported cases of infection by this microorganism in the context of acute hydrops, nor concurrent with <em>Herpes Simplex virus 2</em> infection.</div></div><div><h3>Observations</h3><div>A 33-year-old Portuguese woman of Caucasian ethnicity with a history of keratoconus presented with a red eye and ocular discomfort in the right eye at the Ophthalmology Emergency Department. Initial examination revealed acute hydrops with no epithelial defects nor signs of infection. Posteriorly, she developed dendritic epithelial lesions suggestive of <em>Herpes Simplex</em> virus infection. These lesions progressed, leading to a central corneal infiltrate and descemetocele. Due to perforation of the descemetocele, a tectonic penetrating keratoplasty was successfully performed, and coinfection of <em>Herpes Simplex virus 2</em> and <em>Mycobacterium chelonae</em> was later confirmed through microbiological examination.</div></div><div><h3>Conclusions and importance</h3><div>This is the first reported case of corneal coinfection with <em>Herpes Simplex virus 2</em> and <em>Mycobacterium chelonae</em> in the setting of acute hydrops. The combination of corneal edema, previous viral infection, and prolonged corticosteroid use likely created a “perfect storm” scenario, predisposing the patient to this unusual coinfection. Our findings highlight the need for heightened awareness of atypical infections in patients with acute hydrops and suggest that such complications may alter corneal barrier function. This case contributes to the understanding of complex interactions between corneal conditions and microbial infections.</div></div>","PeriodicalId":47045,"journal":{"name":"IDCases","volume":"39 ","pages":"Article e02176"},"PeriodicalIF":1.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143157746","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 unique case of herpetic keratitis manifesting as recurrent preseptal cellulitis
IF 1.1
IDCases Pub Date : 2025-01-01 DOI: 10.1016/j.idcr.2025.e02187
Emily Miller , Maxwell Ward , Tasaduq Fazili , Ekta Bansal
{"title":"A unique case of herpetic keratitis manifesting as recurrent preseptal cellulitis","authors":"Emily Miller ,&nbsp;Maxwell Ward ,&nbsp;Tasaduq Fazili ,&nbsp;Ekta Bansal","doi":"10.1016/j.idcr.2025.e02187","DOIUrl":"10.1016/j.idcr.2025.e02187","url":null,"abstract":"<div><div>Preseptal cellulitis is typically caused by nasopharyngeal bacteria and can usually be treated with empiric antibiotics. We present a case of herpes simplex virus (HSV) 1 keratitis manifesting as recurrent and treatment refractory preseptal cellulitis. This is a rare presentation that is infrequently reported in the literature. Due to the potential for permanent vision loss, it is important to consider herpes viruses as an etiology in immunocompromised patients with preseptal cellulitis not responding to standard treatment.</div></div>","PeriodicalId":47045,"journal":{"name":"IDCases","volume":"39 ","pages":"Article e02187"},"PeriodicalIF":1.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143387035","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
Ictal vomiting as an unusual presentation of herpes simplex encephalitis ‐ Pathophysiological and therapeutic perspectives
IF 1.1
IDCases Pub Date : 2025-01-01 DOI: 10.1016/j.idcr.2025.e02186
Hosna Elshony , Abdelrahman Idris , Abdulaziz Al-Ghamdi , Rakan Almuhanna , Waleed Amsaib M. Ahmed
{"title":"Ictal vomiting as an unusual presentation of herpes simplex encephalitis ‐ Pathophysiological and therapeutic perspectives","authors":"Hosna Elshony ,&nbsp;Abdelrahman Idris ,&nbsp;Abdulaziz Al-Ghamdi ,&nbsp;Rakan Almuhanna ,&nbsp;Waleed Amsaib M. Ahmed","doi":"10.1016/j.idcr.2025.e02186","DOIUrl":"10.1016/j.idcr.2025.e02186","url":null,"abstract":"<div><h3>Introduction</h3><div>Herpes Simplex Encephalitis (HSE) is a formidable neurological infection that is often challenging to diagnose owing to its diverse clinical manifestations. This case report details the clinical odyssey of a sixty-year-old female with diabetes, hypothyroidism, and hypertension, who presented with fever, vomiting, and evolving neurological symptoms.</div></div><div><h3>Case Presentation</h3><div>The patient's initial admission failed to yield a diagnosis, and her condition worsened, marked by behavioral changes, cognitive decline, and focal seizures. Neuroimaging revealed characteristic findings, confirming non-hemorrhagic herpetic encephalitis. Despite antiviral and antiepileptic therapy, persistent vomiting prompted further investigations, uncovering infrequent right temporal sharp waves on EEG, leading to a diagnosis of \"ictus emiticus.\"</div></div><div><h3>Conclusion</h3><div>This case of Herpes Simplex Encephalitis (HSE) underscores the diverse clinical spectrum and challenges in management. The patient's atypical presentation underscores the importance of considering HSE in patients with fever and unexplained persistent vomiting for early diagnosis and better prognosis.</div><div>Diagnostic tools (neuroimaging, cerebrospinal fluid analysis, and electroencephalography) confirmed HSE involvement in the right temporal lobe, emphasizing the strong association between HSV encephalitis and seizures, which can be explained by various mechanisms.</div><div>Timely antiviral therapy and tailored antiepileptic strategies led to gradual clinical improvement, showcasing the potential of valproate beyond antiepileptic use.</div><div>This case prompts further exploration into HSE's pathophysiology and treatment. It emphasizes individualized patient care and vigilance for potential post-resolution sequelae, contributing to our evolving understanding of HSE.</div></div>","PeriodicalId":47045,"journal":{"name":"IDCases","volume":"39 ","pages":"Article e02186"},"PeriodicalIF":1.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143386997","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
Failure of Gallium-68 citrate to detect large, enhancing, intracerebral central nervous system tuberculomas: A cautionary tale
IF 1.1
IDCases Pub Date : 2025-01-01 DOI: 10.1016/j.idcr.2025.e02155
Selwyn Selva Kumar , Adrian Keith Noronha , Julie Hephzibah , Harshad Arvind Vanjare , Abi Manesh
{"title":"Failure of Gallium-68 citrate to detect large, enhancing, intracerebral central nervous system tuberculomas: A cautionary tale","authors":"Selwyn Selva Kumar ,&nbsp;Adrian Keith Noronha ,&nbsp;Julie Hephzibah ,&nbsp;Harshad Arvind Vanjare ,&nbsp;Abi Manesh","doi":"10.1016/j.idcr.2025.e02155","DOIUrl":"10.1016/j.idcr.2025.e02155","url":null,"abstract":"<div><h3>Background</h3><div>Gallium-68 citrate is an emerging diagnostic tool for the evaluation of infections. Its performance in brain infections is unknown. The available diagnostics for central nervous system tuberculosis are imprecise.</div></div><div><h3>Case presentation</h3><div>We report a patient with large, active, enhancing, microbiologically confirmed tuberculomas in the right frontal lobe, who underwent Gallium-68 PET CT. It did not show any tracer uptake in the tuberculous lesions.</div></div><div><h3>Conclusions</h3><div>We report caution in using Ga-68 PET CT for CNS TB and discuss the potential reasons for this observation.</div></div>","PeriodicalId":47045,"journal":{"name":"IDCases","volume":"40 ","pages":"Article e02155"},"PeriodicalIF":1.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143683207","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
Fusobacterium necrophorum associated with pelvic infections: A case series and literature review 与盆腔感染相关的坏死杆菌:病例系列和文献综述
IF 1.1
IDCases Pub Date : 2025-01-01 DOI: 10.1016/j.idcr.2025.e02190
Manasa Brown , Sabrina Imam , Jade Pagkas-Bather
{"title":"Fusobacterium necrophorum associated with pelvic infections: A case series and literature review","authors":"Manasa Brown ,&nbsp;Sabrina Imam ,&nbsp;Jade Pagkas-Bather","doi":"10.1016/j.idcr.2025.e02190","DOIUrl":"10.1016/j.idcr.2025.e02190","url":null,"abstract":"<div><div><em>Fusobacterium necrophorum</em> is a gram-negative anaerobic bacillus most commonly implicated in oropharyngeal infections and their subsequent complications, including septic thrombophlebitis of the internal jugular vein, or Lemierre syndrome. However, limited case reports document evidence of pelvic infections associated with <em>Fusobacterium</em> as well, such as pelvic peritonitis and pelvic septic vein thrombophlebitis. In this case series, we discuss two occurrences of <em>Fusobacterium necrophorum</em> bacteremia from a presumed gynecologic source and present a literature review of other reported cases of <em>Fusobacterium</em> associated with female pelvic etiology. While current data describe a greater prevalence of <em>Fusobacterium</em> infections overall in men compared to women, more information is needed regarding the clinical significance of female-specific risk factors that may predispose to this disease.</div></div>","PeriodicalId":47045,"journal":{"name":"IDCases","volume":"39 ","pages":"Article e02190"},"PeriodicalIF":1.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143529721","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
Neurobrucellosis manifested by recurrent aseptic meningitis: A case report
IF 1.1
IDCases Pub Date : 2025-01-01 DOI: 10.1016/j.idcr.2025.e02193
Reza Razaghi , Fatemeh Kourkinejad_Gharaei , Forough Faroughi
{"title":"Neurobrucellosis manifested by recurrent aseptic meningitis: A case report","authors":"Reza Razaghi ,&nbsp;Fatemeh Kourkinejad_Gharaei ,&nbsp;Forough Faroughi","doi":"10.1016/j.idcr.2025.e02193","DOIUrl":"10.1016/j.idcr.2025.e02193","url":null,"abstract":"<div><div>Brucellosis is an endemic zoonotic disease in LMIC countries. Neurobrucellosis is a rare and serious complication that affects 3–5 % of cases worldwide. We report the successful treatment of a 31-year-old woman who presented with a chief complaint of headache and nausea. Headache was started six months before admission in the frontal and occipital area with radiation to the neck. The patient hospitalized three times within last six months with diagnosis of aseptic meningitis. Brucellosis, tuberculosis, and syphilis tests and CSF fluid analysis were requested. Neutrophilia and pleocytosis in CSF fluid. Analysis of CSF fluid for cytology and PCR test for HSV-1&amp;2 was negative. Rheumatologic tests for SLE, Behcet's disease and sarcoidosis were also negative. Test results was as follow: Wright: 1/320, Coombs Wright: 1/640, 2ME: 1/160, Brucella IgG: 25(Positive). According to the test results, combined treatment with rifampin, Co-trimoxazole, and ceftriaxone was performed for neurobrucellosis for nine months. Considering the endemic prevalence of brucellosis in this region, the rare manifestations of this disease should be considered.</div></div>","PeriodicalId":47045,"journal":{"name":"IDCases","volume":"40 ","pages":"Article e02193"},"PeriodicalIF":1.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143579986","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
Haemophilus Influenzae Type F as a rare cause of septic arthritis
IF 1.1
IDCases Pub Date : 2025-01-01 DOI: 10.1016/j.idcr.2025.e02204
Charles E. McCafferty , Luke McKinnon , Tristan Rappo
{"title":"Haemophilus Influenzae Type F as a rare cause of septic arthritis","authors":"Charles E. McCafferty ,&nbsp;Luke McKinnon ,&nbsp;Tristan Rappo","doi":"10.1016/j.idcr.2025.e02204","DOIUrl":"10.1016/j.idcr.2025.e02204","url":null,"abstract":"<div><div>IB is an 80-year-old man who presented to our emergency department with acute pain, swelling, and fluctuance of his right knee. Investigations revealed neutrophilia, and acute renal impairment. He was admitted under the orthopaedic team and underwent knee aspiration. Synovial fluid culture yielded Haemophilus Influenzae Type F, a rare cause of septic arthritis. He underwent arthroscopic knee washout and debridement three times during his admission and was commenced on intravenous antibiotics. This case report discusses his clinical course, and the management of Haemophilus</div><div>influenzae septic arthritis.</div></div>","PeriodicalId":47045,"journal":{"name":"IDCases","volume":"40 ","pages":"Article e02204"},"PeriodicalIF":1.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143724709","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
Fever for days: A challenging case of dalbavancin-induced fever
IF 1.1
IDCases Pub Date : 2025-01-01 DOI: 10.1016/j.idcr.2024.e02138
Mohamed A. Almahal , Claire Wan , Benjamin Albrecht , Sarah Green , Ahmed Babiker
{"title":"Fever for days: A challenging case of dalbavancin-induced fever","authors":"Mohamed A. Almahal ,&nbsp;Claire Wan ,&nbsp;Benjamin Albrecht ,&nbsp;Sarah Green ,&nbsp;Ahmed Babiker","doi":"10.1016/j.idcr.2024.e02138","DOIUrl":"10.1016/j.idcr.2024.e02138","url":null,"abstract":"<div><div>Dalbavancin is a novel long acting lipoglycopeptide antibiotic with a favorable safety profile approved for treating Acute Bacterial Skin and Skin Structure Infections (ABSSSI) caused by Gram-positive organisms. Given its long half-life, a two-dose regimen can provide effective systemic therapy for up to six weeks, making it an appealing option to avoid prolonged intravenous antibiotic therapy. Herein, we report a case of a 27-year-old male who developed dalbavancin-induced fever while treating Methicillin-sensitive <em>Staphylococcus aureus</em> (MSSA) bacteremia. Despite being inconsistently reported, our case highlights fever as a possible side effect of dalbavancin therapy, and the challenging management of this adverse event given its prolonged half-life.</div></div>","PeriodicalId":47045,"journal":{"name":"IDCases","volume":"39 ","pages":"Article e02138"},"PeriodicalIF":1.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11750494/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143025292","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
Ceftazidime-resistance in pediatric melioidosis: A case report and literature review
IF 1.1
IDCases Pub Date : 2025-01-01 DOI: 10.1016/j.idcr.2025.e02149
Tonnii Loong-Loong Sia , Charles Dekun Lai , Kamilah Manan , Fu-Lung Khiu , Siti Zakiyyah Bakhtiar , Yek-Kee Chor , Su-Lin Chien , Lee-See Tan , Mong-How Ooi , Anand Mohan
{"title":"Ceftazidime-resistance in pediatric melioidosis: A case report and literature review","authors":"Tonnii Loong-Loong Sia ,&nbsp;Charles Dekun Lai ,&nbsp;Kamilah Manan ,&nbsp;Fu-Lung Khiu ,&nbsp;Siti Zakiyyah Bakhtiar ,&nbsp;Yek-Kee Chor ,&nbsp;Su-Lin Chien ,&nbsp;Lee-See Tan ,&nbsp;Mong-How Ooi ,&nbsp;Anand Mohan","doi":"10.1016/j.idcr.2025.e02149","DOIUrl":"10.1016/j.idcr.2025.e02149","url":null,"abstract":"<div><div>We report a first case of ceftazidime-resistant pediatric melioidosis involving a previously healthy seven-year-old boy who presented with right lobar pneumonia complicated with a 5-cm lung abscess. Ceftazidime was initiated on Day-6 of admission when <em>Burkholderia pseudomallei</em> (ceftazidime-susceptible, minimum inhibitory concentration [MIC] 1.0 mcg/mL) was isolated from blood. Despite ceftazidime therapy at the recommended dosage, he developed fulminant septic shock and respiratory failure on Day-18 of hospitalization, requiring invasive ventilation, hemodynamic support, and continuous renal replacement therapy. His antibiotic was empirically escalated to meropenem; ceftazidime-resistant <em>B. pseudomallei</em> (MIC 32 mcg/mL) was subsequently isolated from blood and endotracheal secretions<em>.</em> He improved after two weeks of intensive care and was discharged well after two months of hospitalization. Our literature review on ceftazidime-resistant <em>B. pseudomallei</em> infection indicates that acquired resistance is a rare but potentially lethal treatment-related complication. All melioidosis patients should be carefully monitored during treatment with ceftazidime (or other β-lactams) for the development of antimicrobial resistance.</div></div>","PeriodicalId":47045,"journal":{"name":"IDCases","volume":"39 ","pages":"Article e02149"},"PeriodicalIF":1.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11773197/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143061122","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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