发布求助
文献互助 智能选刊 最新文献

IDCases最新文献

筛选
英文 中文
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 ,&nbsp;Imen Ben Ismail ,&nbsp;Wafa Ragmoun ,&nbsp;Mokhles Lajmi ,&nbsp;Bochra Zayène ,&nbsp;Islam Mejri ,&nbsp;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
Case report: Dirofilarial infection of the face
IF 1.1
IDCases Pub Date : 2025-01-01 DOI: 10.1016/j.idcr.2024.e02142
Anne Schneider , Jannik Fasse , Dennis Tappe , Christoph Lübbert , Henning Trawinski
{"title":"Case report: Dirofilarial infection of the face","authors":"Anne Schneider ,&nbsp;Jannik Fasse ,&nbsp;Dennis Tappe ,&nbsp;Christoph Lübbert ,&nbsp;Henning Trawinski","doi":"10.1016/j.idcr.2024.e02142","DOIUrl":"10.1016/j.idcr.2024.e02142","url":null,"abstract":"<div><div>An 18-year-old male patient from Ukraine, living in Germany for 2 years, presented with a painless subcutaneous swelling on the left cheek that had been present for several months. Finally, the diagnosis of subcutaneous dirofilariasis caused by <em>Dirofilaria repens</em> was confirmed by 12S rRNA gene PCR and sequencing from tissue by nematode-specific PCRs followed by sequencing after surgical resection of the lesion. Microfilaremia was ruled out and no further treatment was required. Subcutaneous filariasis continues to spread in Central Europe due to climate change, the expansion of vector mosquitoes and the mobility of humans and dogs.</div></div>","PeriodicalId":47045,"journal":{"name":"IDCases","volume":"39 ","pages":"Article e02142"},"PeriodicalIF":1.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11773195/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143061118","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
Bilateral acute macular neuroretinopathy following influenza A infection
IF 1.1
IDCases Pub Date : 2025-01-01 DOI: 10.1016/j.idcr.2025.e02173
Charles W. Ryan , Rajesh C. Rao
{"title":"Bilateral acute macular neuroretinopathy following influenza A infection","authors":"Charles W. Ryan ,&nbsp;Rajesh C. Rao","doi":"10.1016/j.idcr.2025.e02173","DOIUrl":"10.1016/j.idcr.2025.e02173","url":null,"abstract":"<div><div>A previously healthy 18-year-old female presented with bilateral cecocentral scotomas two-days after onset of confirmed Influenza A infection, consistent with a post-viral acute macular neuroretinopathy (AMN). Fundoscopy revealed bilateral small petaloid lightening in the nasal macula, and optical coherence tomography revealed thinning of the interdigitation zone, ellipsoid zone, and outer nuclear layer bilaterally. Scotomas and associated imaging findings showed partial improvement in the weeks following diagnosis. This case demonstrates that AMN may be triggered Influenza A infection, and that resulting scotomas and retinal thinning may improve in the weeks following the initial insult.</div></div>","PeriodicalId":47045,"journal":{"name":"IDCases","volume":"39 ","pages":"Article e02173"},"PeriodicalIF":1.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143340490","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
Hemophagocytic lymphohistiocytosis in a neonate with enterovirus infection: Case report and literature review 肠道病毒感染新生儿嗜血细胞淋巴组织细胞增多症：病例报告和文献综述
IF 1.1
IDCases Pub Date : 2025-01-01 DOI: 10.1016/j.idcr.2025.e02177
Hua Hu , Shukun Yu , Jing Zhang , Hongping Zhang
{"title":"Hemophagocytic lymphohistiocytosis in a neonate with enterovirus infection: Case report and literature review","authors":"Hua Hu ,&nbsp;Shukun Yu ,&nbsp;Jing Zhang ,&nbsp;Hongping Zhang","doi":"10.1016/j.idcr.2025.e02177","DOIUrl":"10.1016/j.idcr.2025.e02177","url":null,"abstract":"<div><div>Viruses are the most common organisms causing hemophagocytic lymphohistiocytosis (HLH), and enterovirus infection is the most frequently diagnosed virus infection in the newborn period. However, in recent years, there have been relatively few reports of enterovirus infection in Chinese neonates complicated by HLH. Here, we describe a female preterm infant who contracted echovirus 11 at day 4 and rapidly developed sepsis during the following three days, along with fever, lethargy, disseminated intravascular coagulation (DIC), and sepsis. She was ultimately identified as having echovirus 11 complicated by HLH. This report will contribute to increasing public awareness of the link between HLH and echo 11 infection, which can aid in early identification and treatment.</div><div><strong>What’s New:</strong> We reported female preterm infant who contracted echovirus 11 at day 4 and rapidly developed sepsis during the following three days, it was the first report from central China that we are aware of.</div></div>","PeriodicalId":47045,"journal":{"name":"IDCases","volume":"40 ","pages":"Article e02177"},"PeriodicalIF":1.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143593428","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
Organizing pneumonia in a patient following treatment of chronic hepatitis B with pegylated interferon alfa-2b: A case report
IF 1.1
IDCases Pub Date : 2025-01-01 DOI: 10.1016/j.idcr.2025.e02191
Bing Tian , Pan Wang , Chun Shan , Cheng Gao , Qun Zhang
{"title":"Organizing pneumonia in a patient following treatment of chronic hepatitis B with pegylated interferon alfa-2b: A case report","authors":"Bing Tian ,&nbsp;Pan Wang ,&nbsp;Chun Shan ,&nbsp;Cheng Gao ,&nbsp;Qun Zhang","doi":"10.1016/j.idcr.2025.e02191","DOIUrl":"10.1016/j.idcr.2025.e02191","url":null,"abstract":"<div><div>Chronic hepatitis B is a major cause of liver disease in China. One of the treatments currently recommended is interferon (IFN). Although uncommon, there have been some case reviews on patients with hepatitis C with pulmonary adverse effects following treatment with IFN. Our case report is of a patient who acquired organizing pneumonia after he was treated for hepatitis B with pegylated IFN alfa-2b. We aim to raise awareness of the pulmonary toxicity of interferon, especially as it is increasingly used to treat patients with chronic hepatitis B.</div></div>","PeriodicalId":47045,"journal":{"name":"IDCases","volume":"39 ","pages":"Article e02191"},"PeriodicalIF":1.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143519872","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 rare case of aortitis and occlusive iliac thrombus due to Campylobacter fetus bacteremia
IF 1.1
IDCases Pub Date : 2025-01-01 DOI: 10.1016/j.idcr.2025.e02198
Malleswari Ravi , Cristine Arcilla , Gurjit Kaeley
{"title":"A rare case of aortitis and occlusive iliac thrombus due to Campylobacter fetus bacteremia","authors":"Malleswari Ravi ,&nbsp;Cristine Arcilla ,&nbsp;Gurjit Kaeley","doi":"10.1016/j.idcr.2025.e02198","DOIUrl":"10.1016/j.idcr.2025.e02198","url":null,"abstract":"<div><div>A 66-year-old male presented with 1-week of fever and generalized weakness. Workup revealed <em>Campylobacter fetus</em> bacteremia. Further investigation with imaging showed distal abdominal aortitis with occlusive thrombus in the right common iliac artery. <em>C. fetus</em> bacteremia with endovascular localization is clinically very rare but with high mortality rate.</div></div>","PeriodicalId":47045,"journal":{"name":"IDCases","volume":"40 ","pages":"Article e02198"},"PeriodicalIF":1.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143726049","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
Abscesses of the spine and iliac fossa caused by infection with the opportunistic bacterium Fusobacterium nucleatum
IF 1.1
IDCases Pub Date : 2025-01-01 DOI: 10.1016/j.idcr.2025.e02205
YunTao Gu , Yuan Zhou , TianQiong Hu , Hai Zhao , YongPing Wang , YongXiong He
{"title":"Abscesses of the spine and iliac fossa caused by infection with the opportunistic bacterium Fusobacterium nucleatum","authors":"YunTao Gu ,&nbsp;Yuan Zhou ,&nbsp;TianQiong Hu ,&nbsp;Hai Zhao ,&nbsp;YongPing Wang ,&nbsp;YongXiong He","doi":"10.1016/j.idcr.2025.e02205","DOIUrl":"10.1016/j.idcr.2025.e02205","url":null,"abstract":"<div><div>We present a case of spinal and iliac fossa infection caused by <em>Fusobacterium nucleatum</em> in a 52-year-old male patient with unexplained back pain. Notably, the patient had no history of periodontal infections.Magnetic resonance imaging (MRI) revealed abscesses at the L3-4 vertebrae and hip, with dura mater and cauda equina compression.Next-generation sequencing (NGS) of the aspirate confirmed the presence of <em>Fusobacterium nucleatum</em>. The patient was treated with antibiotics (carbapenems, and metronidazole) and underwent surgical procedures for abscess drainage and internal fixation, resulting in the removal of 1000 ml of pus. Following a 46-day recovery period, the patient made a full recovery.This rare infection poses a significant diagnostic challenge due to its insidious onset and low blood culture sensitivity. The role of next-generation sequencing (NGS) in this context is paramount, as it has been instrumental in arriving at an accurate diagnosis and formulating an effective treatment plan. In view of the challenges posed by this infection, NGS emerges as a crucial tool for the diagnosis and management of unexplained infections.</div></div>","PeriodicalId":47045,"journal":{"name":"IDCases","volume":"40 ","pages":"Article e02205"},"PeriodicalIF":1.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143724710","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
Unusual syphilis manifestation: From breast implant rupture to systemic erythroderma
IF 1.1
IDCases Pub Date : 2025-01-01 DOI: 10.1016/j.idcr.2025.e02170
Vivien Moris , Eliott Laine , Sahal Khan , Leslie Ann See
{"title":"Unusual syphilis manifestation: From breast implant rupture to systemic erythroderma","authors":"Vivien Moris ,&nbsp;Eliott Laine ,&nbsp;Sahal Khan ,&nbsp;Leslie Ann See","doi":"10.1016/j.idcr.2025.e02170","DOIUrl":"10.1016/j.idcr.2025.e02170","url":null,"abstract":"<div><div>This case report describes a rare and unusual manifestation of syphilis in a 55-year-old transgender female with a history of breast implant surgery. The patient presented with a painless enlargement of the right breast, accompanied by pruritus and skin lesions. Initial misdiagnosis led to treatment for scabies, which worsened into diffuse erythroderma. Further examination revealed breast implant rupture and systemic lymphadenopathy. Surgical removal of the implant and seroma drainage was performed. Pathological findings showed chronic inflammation, with concerns about a cutaneous T-cell lymphoproliferative disorder, but no signs of malignancy were observed. Serological tests confirmed active syphilis with a positive TPHA titer and VDRL result. This case highlights the importance of considering infectious etiologies, such as syphilis, even in patients with atypical clinical presentations, including those involving breast implants and skin conditions. Timely diagnosis and appropriate management are critical to prevent systemic complications in similar cases.</div></div>","PeriodicalId":47045,"journal":{"name":"IDCases","volume":"39 ","pages":"Article e02170"},"PeriodicalIF":1.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143158153","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
Human parvovirus B19 as an unusual cause of Guillain-Barré syndrome: A case report 人细小病毒B19是引起格林-巴- <s:1>综合征的一种罕见病因：1例报告。
IF 1.1
IDCases Pub Date : 2025-01-01 DOI: 10.1016/j.idcr.2024.e02135
Elisa Creuzet , Wendy Pulby , Claire Dupuis , Christine Archimbaud , Amélie Brebion , Hélène Chabrolles , Mathilde Picard , Christel Regagnon , Audrey Mirand , Bertrand Souweine , Cécile Henquell
{"title":"Human parvovirus B19 as an unusual cause of Guillain-Barré syndrome: A case report","authors":"Elisa Creuzet ,&nbsp;Wendy Pulby ,&nbsp;Claire Dupuis ,&nbsp;Christine Archimbaud ,&nbsp;Amélie Brebion ,&nbsp;Hélène Chabrolles ,&nbsp;Mathilde Picard ,&nbsp;Christel Regagnon ,&nbsp;Audrey Mirand ,&nbsp;Bertrand Souweine ,&nbsp;Cécile Henquell","doi":"10.1016/j.idcr.2024.e02135","DOIUrl":"10.1016/j.idcr.2024.e02135","url":null,"abstract":"<div><div>Human Parvovirus B19 (B19V) is rarely observed in patients with Guillain-Barré syndrome. We report the case of a patient with rapidly progressive functional impotence of the limbs. B19V was detected in both blood and CSF samples. The patient improved clinically after plasma exchanges, but mild functional impotence persisted 2 months later.</div></div>","PeriodicalId":47045,"journal":{"name":"IDCases","volume":"39 ","pages":"Article e02135"},"PeriodicalIF":1.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11728891/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142980025","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
Ecthyma amidst the global monkeypox outbreak: A key differential? —A case series 全球猴痘爆发中的湿疹：一个关键的区别？-一个案例系列。
IF 1.1
IDCases Pub Date : 2025-01-01 DOI: 10.1016/j.idcr.2024.e02125
Houriah Y. Nukaly , Waseem K. Alhawsawi , Jumanah Y. Nassar , Aymen Alharbi , Sarah Tayeb , Nada Rabie , Moayad Alqurashi , Raghda Faraj , Rehab Fadag , Mohammed Samannodi
{"title":"Ecthyma amidst the global monkeypox outbreak: A key differential? —A case series","authors":"Houriah Y. Nukaly ,&nbsp;Waseem K. Alhawsawi ,&nbsp;Jumanah Y. Nassar ,&nbsp;Aymen Alharbi ,&nbsp;Sarah Tayeb ,&nbsp;Nada Rabie ,&nbsp;Moayad Alqurashi ,&nbsp;Raghda Faraj ,&nbsp;Rehab Fadag ,&nbsp;Mohammed Samannodi","doi":"10.1016/j.idcr.2024.e02125","DOIUrl":"10.1016/j.idcr.2024.e02125","url":null,"abstract":"<div><h3>Background</h3><div>Ecthyma is a deeper form of impetigo involving the epidermis and dermis causing ulcerative plaques. Pathogens commonly responsible for the disease (group A beta-hemolytic streptococcus and Staphylococcus aureus) typically afflicts children, presenting during early stages with skin lesions that can closely resemble other vesicular and ulcerative dermatoses, such as those observed in mpox infection. The ongoing global outbreak of monkeypox has escalated the urgency for clinicians to accurately differentiate between these conditions due to their overlapping dermatological manifestations. Through this series, we intend to demonstrate the diverse clinical presentations of ecthyma observed in non-endemic regions, which may closely mimic those of monkeypox.</div></div><div><h3>Case presentation</h3><div>The first case describes a 12- year-old male with a history of atopic dermatitis, presenting with a vesicular rash initially suspected to be monkeypox. However, diagnosis via skin punch biopsy and cultures revealed ecthyma. The second case involved an 18-year-old male with acute, rapidly progressing ulcerated lesions and systemic symptoms. Differential diagnosis included toxic shock syndrome and necrotizing fasciitis, but histopathological findings confirmed ecthyma. The third case featured a 55-year-old woman with rapidly developing skin lesions on her hand, resolved through empirical antibiotic therapy, further confirming the diagnosis.</div></div><div><h3>Conclusion</h3><div>misdiagnosis and thus, delayed treatment of ecthyma leads to severe unfavourable outcomes. Given its rare occurrence yet fatal potential, and the current global vigilance due to the monkeypox outbreak, it is vital for healthcare providers to include ecthyma in the differential diagnosis of necrotic and ulcerative skin lesions.</div></div>","PeriodicalId":47045,"journal":{"name":"IDCases","volume":"39 ","pages":"Article e02125"},"PeriodicalIF":1.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11731615/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142984913","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
首页 上一页 下一页 尾页
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整，为了账户安全，请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
请完成安全验证×
相关产品
×
本文献相关产品
联系我们：info@booksci.cn Book学术提供免费学术资源搜索服务，方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号：481959085
Book学术官方微信