Radiology Case Reports最新文献_第6页

Iatrogenic chest tube placement within the heart following a large pneumothorax 严重气胸后的医源性胸管置入

Radiology Case Reports Pub Date : 2025-05-20 DOI: 10.1016/j.radcr.2025.04.089

Shervin Zoghi BS, BA , Cameron L. Brock MD , Kwame Atsina MD , Yasser G. Abdelhafez MD, PhD , Fatma Sen MD , Lorenzo Nardo MD, PhD , Mohammad H. Madani MD

引用次数: 0

Convulsive status epilepticus revealing cerebral microbleeds in a pediatric patient: A rare case report 惊厥癫痫持续状态显示脑微出血的儿科患者：一个罕见的病例报告

Radiology Case Reports Pub Date : 2025-05-20 DOI: 10.1016/j.radcr.2025.04.030

Siham Oukassem, Chaimae Jabbari, Chaimae Abourak, Asmae Guennouni, Lina Belkouchi, Siham El Haddad, Nazik Allali, Latifa Chat

引用次数: 0

Successful long-term survival following lipiodol chemoembolization for hepatocellular carcinoma in Alagille syndrome: A case report 脂醇化疗栓塞治疗肝细胞癌Alagille综合征后成功的长期生存：1例报告

Radiology Case Reports Pub Date : 2025-05-20 DOI: 10.1016/j.radcr.2025.04.125

Imad Akasbi MD , Ismail Chaouche MD , Nizar El Bouardi MD , Amal Akammar MD , Hajar O Chahdi MD , Ismail Zerrari MD , Maria Lahlali MD , Hakima Abid MD , Badr Alami MD , Nada Lahmidani MD , Meryem Boubbou MD , Ibrahimi Sidi adil MD , Mustapha Maaroufi MD , MY Youssef Alaoui Lamrani MD

{"title":"Successful long-term survival following lipiodol chemoembolization for hepatocellular carcinoma in Alagille syndrome: A case report","authors":"Imad Akasbi MD , Ismail Chaouche MD , Nizar El Bouardi MD , Amal Akammar MD , Hajar O Chahdi MD , Ismail Zerrari MD , Maria Lahlali MD , Hakima Abid MD , Badr Alami MD , Nada Lahmidani MD , Meryem Boubbou MD , Ibrahimi Sidi adil MD , Mustapha Maaroufi MD , MY Youssef Alaoui Lamrani MD","doi":"10.1016/j.radcr.2025.04.125","DOIUrl":"10.1016/j.radcr.2025.04.125","url":null,"abstract":"<div><div>Alagille syndrome is a rare genetic disorder causing multisystem complications, including biliary abnormalities, chronic liver disease, and rarely, hepatocellular carcinoma (HCC), which is difficult to manage due to liver dysfunction and vascular abnormalities. We report a 29-year-old female, diagnosed with Alagille syndrome in infancy, who developed infiltrative HCC at age 20 and underwent lipiodol-based transarterial chemoembolization (TACE) in 2015, with a second session in 2016 for recurrence. Remarkably, she has achieved an exceptional 9-year survival post-treatment with stable imaging and no recurrence, a highly uncommon outcome for HCC in Alagille syndrome, highlighting TACE’s potential as an effective palliative treatment for HCC in Alagille syndrome, particularly for patient's ineligible for liver transplantation, and underscoring the need for further studies on locoregional therapies in this rare population.</div></div>","PeriodicalId":53472,"journal":{"name":"Radiology Case Reports","volume":"20 8","pages":"Pages 3879-3885"},"PeriodicalIF":0.0,"publicationDate":"2025-05-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144090609","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Endovascular treatment of cirsoid aneurysms: A stepwise approach to successful embolization 颅内动脉瘤的血管内治疗：成功栓塞的分步方法

Radiology Case Reports Pub Date : 2025-05-17 DOI: 10.1016/j.radcr.2025.04.070

Ronak Patel MD , Parker Mitchell MD , Mohadese Ahmadzade MD , Mohammad Ghasemi-Rad MD , Ravi Kaushikkumar Shastri MD

{"title":"Endovascular treatment of cirsoid aneurysms: A stepwise approach to successful embolization","authors":"Ronak Patel MD , Parker Mitchell MD , Mohadese Ahmadzade MD , Mohammad Ghasemi-Rad MD , Ravi Kaushikkumar Shastri MD","doi":"10.1016/j.radcr.2025.04.070","DOIUrl":"10.1016/j.radcr.2025.04.070","url":null,"abstract":"<div><div>Cirsoid aneurysms, a subtype of arteriovenous fistulas (AVF), of the scalp are rare pathological lesions characterized by abnormal fistulous connections between superficial arteries and draining veins without intervening capillary beds. We present a case report of a cirsoid aneurysm located on the scalp, treated at our tertiary care center using percutaneous endovascular intervention with injection embolics. This report highlights the challenges posed by complex vascular anatomy and high shunt flow in the treatment of such lesions involving the head and neck. We discuss the rationale for selecting the treatment approach, emphasizing the importance of a patient-specific strategy to achieve successful obliteration of the abnormal vascular connections. Our experience underscores the efficacy of transarterial and/or transvenous embolization using appropriate embolic materials in the management of cirsoid aneurysms. This case report contributes to the existing literature on treatment options for scalp AVFs, providing insights into optimizing outcomes in these rare but clinically significant lesions.</div></div>","PeriodicalId":53472,"journal":{"name":"Radiology Case Reports","volume":"20 8","pages":"Pages 3865-3869"},"PeriodicalIF":0.0,"publicationDate":"2025-05-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144072339","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Orbital apex syndrome associated with cranial nerve V neuritis complicating bacterial maxillary sinusitis 眶尖综合征与颅神经V神经炎合并细菌性上颌窦炎

Radiology Case Reports Pub Date : 2025-05-17 DOI: 10.1016/j.radcr.2025.04.111

Houssam Rajad , Soufiane Bigi , Said Adnor , Zakaria Chahbi , Abderrahmane Ibenyahia , Mounir Salek , Mohamed Amine Baba , Ahmed Kharbach , Abderrahmane Achbani , Hajar El Agouri , Majdouline Obtel , Soukaina Wakrim

{"title":"Orbital apex syndrome associated with cranial nerve V neuritis complicating bacterial maxillary sinusitis","authors":"Houssam Rajad , Soufiane Bigi , Said Adnor , Zakaria Chahbi , Abderrahmane Ibenyahia , Mounir Salek , Mohamed Amine Baba , Ahmed Kharbach , Abderrahmane Achbani , Hajar El Agouri , Majdouline Obtel , Soukaina Wakrim","doi":"10.1016/j.radcr.2025.04.111","DOIUrl":"10.1016/j.radcr.2025.04.111","url":null,"abstract":"<div><div>Maxillary sinusitis is a common pathology of the paranasal sinuses, most frequently caused by bacterial infections. Although typically benign, it can occasionally lead to severe complications when the infectious process extends beyond the sinus cavity. One such rare but serious complication is orbital apex syndrome (OAS), also known as Jacod syndrome, characterized by dysfunction of multiple cranial nerves at the orbital apex.</div><div>OAS may result from various etiologies, including infectious, traumatic, and neoplastic causes. Among infectious origins, bacterial maxillary sinusitis is an uncommon yet clinically significant contributor. Involvement of the trigeminal nerve (cranial nerve V), manifesting as neuritis, adds further complexity to the clinical presentation.</div><div>Accurate diagnosis and timely management of OAS rely heavily on advanced radiological imaging, particularly magnetic resonance imaging (MRI). MRI plays a pivotal role in confirming the diagnosis, excluding differential diagnoses, and delineating the extent of sinus infection, orbital inflammation, and perineural involvement, including neuritis of cranial nerve V. These imaging findings are essential for guiding appropriate therapeutic strategies.</div><div>In this case report, we describe a rare instance of orbital apex syndrome associated with cranial nerve V neuritis complicating bacterial maxillary sinusitis. The objective is to underscore the crucial role of MRI in both diagnosis and therapeutic decision-making, and to illustrate the characteristic radiological features observed in such cases.</div></div>","PeriodicalId":53472,"journal":{"name":"Radiology Case Reports","volume":"20 8","pages":"Pages 3859-3864"},"PeriodicalIF":0.0,"publicationDate":"2025-05-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144071236","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Polyostotic fibrous dysplasia: Unveiling the complexity of a rare bone disorder through a case report 多骨纤维发育不良：通过一个病例报告揭示罕见骨疾病的复杂性

Radiology Case Reports Pub Date : 2025-05-17 DOI: 10.1016/j.radcr.2025.04.040

Siham Nasri , Hicham Benramdane , Imane Kamaoui , Imane Skiker

引用次数: 0

Dumbbell-shaped hypoglossal schwannoma with cystic and hemorrhagic degeneration: A case report of a rare entity 哑铃形舌下神经鞘瘤伴囊性及出血性变性：一例罕见病例

Radiology Case Reports Pub Date : 2025-05-17 DOI: 10.1016/j.radcr.2025.04.074

Kaouthar Sfar, Fadwa Jaheddine, Kaoutar Maslouhi, Fatima Chait, Meriem Zhim, Najwa ECH-cherif El Kettani, Meriem Fikri, Mohamed Jiddane, Firdaous Touarsa

{"title":"Dumbbell-shaped hypoglossal schwannoma with cystic and hemorrhagic degeneration: A case report of a rare entity","authors":"Kaouthar Sfar, Fadwa Jaheddine, Kaoutar Maslouhi, Fatima Chait, Meriem Zhim, Najwa ECH-cherif El Kettani, Meriem Fikri, Mohamed Jiddane, Firdaous Touarsa","doi":"10.1016/j.radcr.2025.04.074","DOIUrl":"10.1016/j.radcr.2025.04.074","url":null,"abstract":"<div><div>Hypoglossal schwannoma (HS) is a rare, benign tumor arising from the myelin-producing Schwann cells of the twelfth cranial nerve. This tumor typically appears as solid mass, with cystic patterns being extremely rare. A. Kaye classified HS into 3 types based on their origin: type A, completely intracranial; type B, intracranial with extracranial extension via the hypoglossal canal, often referred to as \"dumbbell-shaped\"; and type C, arising solely from the extracranial portion of the XII nerve. Tongue deviation and hypotrophy are the most common symptoms. MRI is the gold standard for accurately characterizing the lesion's features and assessing its relationship with the surrounding structures, while high-resolution CT scan of the skull base is valuable for surgical planning. The treatment of hypoglossal schwannoma (HS) is surgical excision. Advances in microsurgical techniques, radiosurgery and neurophysiological monitoring have significantly reduced mortality and morbidity. Here, we report a case of cystic dumbbell-shaped hypoglossal schwannoma in a 71-year-old woman, aiming to emphasize the clinical and radiological characteristics of this rare entity.</div></div>","PeriodicalId":53472,"journal":{"name":"Radiology Case Reports","volume":"20 8","pages":"Pages 3851-3854"},"PeriodicalIF":0.0,"publicationDate":"2025-05-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144071238","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Hereditary pulmonary alveolar proteinosis in a 5-year-old child: Diagnostic insights and therapeutic approach 遗传性肺泡蛋白沉积症在5岁儿童：诊断见解和治疗方法

Radiology Case Reports Pub Date : 2025-05-17 DOI: 10.1016/j.radcr.2025.04.094

Dhiran Sivasubramanian MBBS , Karthick Balasubramanian MBBS , Sathwik Sanil MBBS , Smrti Aravind MBBS , Virushnee Senthilkumar MBBS

{"title":"Hereditary pulmonary alveolar proteinosis in a 5-year-old child: Diagnostic insights and therapeutic approach","authors":"Dhiran Sivasubramanian MBBS , Karthick Balasubramanian MBBS , Sathwik Sanil MBBS , Smrti Aravind MBBS , Virushnee Senthilkumar MBBS","doi":"10.1016/j.radcr.2025.04.094","DOIUrl":"10.1016/j.radcr.2025.04.094","url":null,"abstract":"<div><div>Hereditary pulmonary alveolar proteinosis (hPAP) is a rare disorder caused by mutations in the CSF2RA or CSF2RB genes, leading to impaired surfactant clearance by alveolar macrophages and subsequent respiratory dysfunction. A 5-year-old female with a 2-year history of poor weight gain, fatigue, and intermittent fever was evaluated. Clinical evaluation revealed hypoxemia, while high-resolution computed tomography (HRCT) of the chest showed the characteristic “crazy-paving” pattern suggestive of PAP. Bronchoalveolar lavage (BAL) yielded milky fluid with periodic acid-Schiff (PAS)-positive material, and genetic testing confirmed a homozygous mutation in the CSF2RA gene, consistent with hPAP. The patient underwent therapeutic whole lung lavage (WLL), resulting in significant clinical improvement. This case underscores the challenges of diagnosing pediatric hPAP and the value of integrating imaging, pathology, and genetic testing. While WLL remains the mainstay of treatment, further research is needed to develop targeted therapies.</div></div>","PeriodicalId":53472,"journal":{"name":"Radiology Case Reports","volume":"20 8","pages":"Pages 3855-3858"},"PeriodicalIF":0.0,"publicationDate":"2025-05-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144071239","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Lumbar puncture resulting in lumbar artery perforation and hypotension: A case report 腰椎穿刺导致腰动脉穿孔和低血压：1例报告

Radiology Case Reports Pub Date : 2025-05-16 DOI: 10.1016/j.radcr.2025.04.016

Anthony D’Angelo MS , Mbinui Ghogomu MS , Zahra Akhtar MD , Hasan Khan MD

引用次数: 0

Breaking the 12-hour barrier: A case report on stent-retriever mechanical thrombectomy in a late-presenting acute ischemic stroke 突破12小时障碍：支架取栓器机械取栓治疗晚期急性缺血性脑卒中一例报告

Radiology Case Reports Pub Date : 2025-05-16 DOI: 10.1016/j.radcr.2025.04.043

Jacub Pandelaki MD, PhD , Krishna Pandu Wicaksono MD, PhD , Heltara Ramandika MD , Dessy Natalia Purba MD , Rizkya Amelia MD , Olivia Ardini MD , Jason MD

引用次数: 0