IDCases最新文献_第6页

A rare neurological complication of dengue: Guillain-Barré Syndrome in a dengue fever patient

IF 1.1

IDCases Pub Date : 2025-01-01 DOI: 10.1016/j.idcr.2025.e02160

Ibrahim Nagmeldin Hassan , Siddig Yaqub , Mohamed Ibrahim , Ghada Aljaili , Nagmeldin Abuassa

{"title":"A rare neurological complication of dengue: Guillain-Barré Syndrome in a dengue fever patient","authors":"Ibrahim Nagmeldin Hassan , Siddig Yaqub , Mohamed Ibrahim , Ghada Aljaili , Nagmeldin Abuassa","doi":"10.1016/j.idcr.2025.e02160","DOIUrl":"10.1016/j.idcr.2025.e02160","url":null,"abstract":"<div><h3>Background</h3><div>Dengue fever is a common viral illness in tropical and subtropical regions, typically presenting with fever, myalgia, and hemorrhagic symptoms. While neurological complications are rare, Guillain-Barré Syndrome (GBS) is a known but uncommon sequelae of viral infections, including dengue.</div></div><div><h3>Case presentation</h3><div>We report the case of a previously healthy 32-year-old male who developed acute flaccid paralysis secondary to GBS following a dengue fever infection. The patient initially presented with classic dengue symptoms—fever, severe headache, retro-orbital pain, and myalgia. Following resolution of the acute dengue phase, he developed ascending muscle weakness, areflexia, and numbness in both legs. Electromyography confirmed a diagnosis of GBS, and cerebrospinal fluid analysis revealed albuminocytologic dissociation. The patient was treated with intravenous immunoglobulin (IVIG), leading to significant clinical improvement, with gradual recovery of motor function.</div></div><div><h3>Discussion</h3><div>This case highlights the rare but significant neurological complication of GBS following dengue fever. Clinicians should maintain a high index of suspicion for GBS in patients recovering from dengue, especially in endemic regions. Early diagnosis and treatment with IVIG or plasmapheresis are critical for improving outcomes in these patients.</div></div><div><h3>Conclusion</h3><div>Dengue fever can lead to severe neurological sequelae such as GBS, and early recognition and intervention can prevent long-term disability. This case underscores the need for vigilance in identifying such complications in patients recovering from viral infections.</div></div>","PeriodicalId":47045,"journal":{"name":"IDCases","volume":"39 ","pages":"Article e02160"},"PeriodicalIF":1.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143158932","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

Otomyiasis caused by Lucilia Sericata: A case report

IF 1.1

IDCases Pub Date : 2025-01-01 DOI: 10.1016/j.idcr.2025.e02163

Makram Tbini , Chaima Ben Ammar , Ines Riahi , Mabrouk Chamakh , Mamia Ben Salah

引用次数: 0

Unusual findings in diarrheal disease: Detection of a microscopic entity of unclear significance

IF 1.1

IDCases Pub Date : 2025-01-01 DOI: 10.1016/j.idcr.2025.e02189

J. Zintgraff , M. Peña , V. Di Matteo , R. Astesana , A. Fernández Garcés , G. Astudillo

引用次数: 0

Intracellular but not undetectable: A case of Francisella tularensis pericarditis

IF 1.1

IDCases Pub Date : 2025-01-01 DOI: 10.1016/j.idcr.2024.e02145

Nicholas P. Bergeron , Cameron G. Gmehlin , Haris Akhtar , Kemar O. Barrett , Sara S. Inglis , Lawrence J. Sinak , Charanjit S. Rihal , Daniel C. DeSimone

引用次数: 0

A case of acute community-acquired pneumonia caused by Tropheryma whipplei in pregnant woman without predisposing medical conditions 一例由 Tropheryma whipplei 引起的急性社区获得性肺炎病例，孕妇无诱发疾病。

IF 1.1

IDCases Pub Date : 2025-01-01 DOI: 10.1016/j.idcr.2024.e02123

Hao Wang , Hongna Yang

引用次数: 0

Blasto-ing through the chest wall: Empyema necessitans due to pulmonary blastomycosis

IF 1.1

IDCases Pub Date : 2025-01-01 DOI: 10.1016/j.idcr.2025.e02185

Cameron G. Gmehlin , Nicholas P. Bergeron , Vaishnavi Ramesh , Haris Akhtar , Zelalem Temesgen

引用次数: 0

Two patients with endometriosis require peripregnancy surgical treatment for pelvic abscesses after egg collection and embryo transfer

IF 1.1

IDCases Pub Date : 2025-01-01 DOI: 10.1016/j.idcr.2025.e02184

Tatsunori Shiraishi , Masafumi Toyoshima , Masao Ichikawa , Shigeo Akira

引用次数: 0

The cruciality of increasing index of suspicion for atypical Bartonella henselae in pediatric patients: A case series

IF 1.1

IDCases Pub Date : 2025-01-01 DOI: 10.1016/j.idcr.2025.e02192

Victoria Vazquez , Lorraine Bermudez-Rivera , Arino Neto , Vanessa Perez , Adriana Cadilla , Linette Sande

{"title":"The cruciality of increasing index of suspicion for atypical Bartonella henselae in pediatric patients: A case series","authors":"Victoria Vazquez , Lorraine Bermudez-Rivera , Arino Neto , Vanessa Perez , Adriana Cadilla , Linette Sande","doi":"10.1016/j.idcr.2025.e02192","DOIUrl":"10.1016/j.idcr.2025.e02192","url":null,"abstract":"<div><div><em>Bartonella henselae</em>, a gram-negative rod, is the etiologic agent of cat scratch disease, which may manifest as a self-limiting local infection or as an atypical, invasive disease. Establishing <em>B. henselae</em> as the causative organism can be challenging as it is a fastidious organism that does not grow on traditional media. Diagnosis is generally performed with serology, which has variable turnaround times, or microbial cell-free DNA (mcfDNA) sequencing, which has a high cost. Therefore, a high index of suspicion is necessary for timely diagnosis and management of these invasive infections. We depict a case series of nine atypical Bartonella infections in children. By highlighting these presentations, their diagnostic testing, and treatment, we emphasize the significance of an elevated index of suspicion of atypical bartonellosis for accurate diagnosis and timely antibiotic management. Our invasive Bartonella cases entail culture-negative subacute endocarditis, osteomyelitis, neuroretinitis, encephalitis, hepatosplenic disease, and lymphadenopathy with splenic involvement.</div></div>","PeriodicalId":47045,"journal":{"name":"IDCases","volume":"40 ","pages":"Article e02192"},"PeriodicalIF":1.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143593429","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 fatal case of disseminated Cladophialophora bantiana infection in a renal transplant recipient 肾移植受者弥散性班提亚氏克氏菌感染1例死亡。

IF 1.1

IDCases Pub Date : 2025-01-01 DOI: 10.1016/j.idcr.2024.e02128

Kali Maniam , Rabeeya Sabzwari , Daniel Carlsen

{"title":"A fatal case of disseminated Cladophialophora bantiana infection in a renal transplant recipient","authors":"Kali Maniam , Rabeeya Sabzwari , Daniel Carlsen","doi":"10.1016/j.idcr.2024.e02128","DOIUrl":"10.1016/j.idcr.2024.e02128","url":null,"abstract":"<div><div>Dematiaceous molds often cause noninvasive disease but have the potential to cause disseminated infection, particularly in immunosuppressed hosts. <em>Cladophialophora bantiana</em> is the most neurotropic of dematiaceous molds and is associated with brain abscesses, but disseminated infection is quite rare. Here we present a case of disseminated <em>C. bantiana</em> in a 67-year-old renal transplant recipient with multifocal soft tissue, bone and presumed central nervous system involvement. <em>C. bantiana</em> infections have been associated with significant mortality and our patient had progression of his disease despite intensive dual antifungal therapy with close therapeutic drug monitoring. There was a delay in diagnosis and initiation of antifungal therapy as the multifocal disease was presumed to represent a malignant process. This case review highlights the importance of having a high index of suspicion for disseminated fungal infection in immunocompromised patients and the need for tissue biopsy to aid in the prompt and timely diagnosis and initiation of empiric antifungal therapy, with concomitant surgical management whenever possible to improve patient outcomes.</div></div>","PeriodicalId":47045,"journal":{"name":"IDCases","volume":"39 ","pages":"Article e02128"},"PeriodicalIF":1.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11728889/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142979898","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

Pulmonary hydatid cyst misdiagnosed as lung cancer 肺水瘤囊肿被误诊为肺癌。

IF 1.1

IDCases Pub Date : 2025-01-01 DOI: 10.1016/j.idcr.2024.e02133

Houssem Messaoudi , Imen Ben Ismail , Wafa Ragmoun , Mokhles Lajmi , Bochra Zayène , Islam Mejri , Saber Hachicha

{"title":"Pulmonary hydatid cyst misdiagnosed as lung cancer","authors":"Houssem Messaoudi , Imen Ben Ismail , Wafa Ragmoun , Mokhles Lajmi , Bochra Zayène , Islam Mejri , Saber Hachicha","doi":"10.1016/j.idcr.2024.e02133","DOIUrl":"10.1016/j.idcr.2024.e02133","url":null,"abstract":"<div><div>Hydatid disease is endemic in Tunisia. Whereas uncomplicated pulmonary hydatid cysts are easily diagnosed on radiological findings, complicated and atypical forms may be misdiagnosed and confused with other pulmonary lesions, mainly lung malignancies. We report a case of a 47-year-old woman, who presented with a 3-month history of hemoptysis. Physical examination was normal. Chest x-ray and CT scan of the chest revealed a mass with speculated margins and central necrosis, located in the apical segment of the right lower lobe moderately contrast-enhanced. The scan guided biopsy showed inflammatory pulmonary parenchyma with no signs of malignancy. Fiberoptic bronchoscopy revealed significant bleeding from the superior segmental bronchus of right lower lobe. Pathology examination of the bronchial aspiration revealed a suggestive aspect of malignant cells. Regarding those findings, lung carcinoma was highly suspected and the importance of hemoptysis motivated an urgent hemostasis lobectomy. The patient underwent a right lower lobectomy with radical lymph node dissection via a right posterolateral thoracotomy. Histological examination showed a laminated membrane lined by a proligerous membrane made up of a layer of eosinophilic cells confirming the diagnosis of pulmonary hydatid cyst. It should be kept in mind that pulmonary hydatid disease can clinically, radiologically mimic lung cancer. Exceptionally, even cytology can lead to a diagnosis pitfall.</div></div>","PeriodicalId":47045,"journal":{"name":"IDCases","volume":"39 ","pages":"Article e02133"},"PeriodicalIF":1.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11729004/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142980026","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