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Edorium Journal of Radiology最新文献

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Post-traumatic duodenal rupture: A case report 创伤后十二指肠破裂：病例报告
Edorium Journal of Radiology Pub Date : 2024-06-11 DOI: 10.5348/100026r02cl2024cr
Chaimae Lahlou, Hadj Hssain Ihssan, Kaoutar Meslouhi, Ouzzaouit Hamza, Hrora Malek, Jroundi Laila, Laamrani Fatima-Zahrae, El Aoufir Omar
{"title":"Post-traumatic duodenal rupture: A case report","authors":"Chaimae Lahlou, Hadj Hssain Ihssan, Kaoutar Meslouhi, Ouzzaouit Hamza, Hrora Malek, Jroundi Laila, Laamrani Fatima-Zahrae, El Aoufir Omar","doi":"10.5348/100026r02cl2024cr","DOIUrl":"https://doi.org/10.5348/100026r02cl2024cr","url":null,"abstract":"\u0000 Post-traumatic duodenal ruptures are rare. Diagnosis remains difficult due to the anatomical characteristics of the duodenum. Medical observation: the authors report a case of post-traumatic duodenal rupture following a road traffic accident, diagnosed on computed tomography (CT) and treated surgically. Although rare, duodenal ruptures are an emergency for all radiologists. The anatomical complexity of the duodeno-pancreatic region and its proximity to vascular and mesenteric structures explain the rich semiology. Careful radiological analysis is essential to facilitate the surgical procedure. Duodenal rupture is an emergency to be aware of and investigated in all cases of road trauma, especially in the case of blunt trauma. Diagnosis is based on CT scan.\u0000","PeriodicalId":269581,"journal":{"name":"Edorium Journal of Radiology","volume":"11 9","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-06-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141357565","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
A giant colloid cyst of the third ventricle: A case report 第三脑室巨大胶样囊肿：病例报告
Edorium Journal of Radiology Pub Date : 2024-01-31 DOI: 10.5348/100025r02bn2024cr
Boujida Nadia, Messaoud Ola, Lahfidi Amal, Kettani Ech-Chrif Najwa, Fikri Meriem, Touarsa Firdaous
{"title":"A giant colloid cyst of the third ventricle: A case report","authors":"Boujida Nadia, Messaoud Ola, Lahfidi Amal, Kettani Ech-Chrif Najwa, Fikri Meriem, Touarsa Firdaous","doi":"10.5348/100025r02bn2024cr","DOIUrl":"https://doi.org/10.5348/100025r02bn2024cr","url":null,"abstract":"\u0000 Colloid cysts of the third ventricle constitute approximately 1% of all intracranial tumors, and they represent the most prevalent form of neuro-epithelial cysts. They are rare, benign cystic lesions with a wide clinical spectrum, but headache is usually dominant. A large cyst may appear in conjunction with an intracranial hypertension syndrome. Additionally, they can induce obstructive hydrocephalus, resulting in rapid acute neurological decline and, in some cases, sudden death. In this study, our aim is to present the clinical manifestations and radiological features of a giant recurrent colloid cyst of the third ventricle by presenting a case of a 55-year-old female patient, reporting a 2-month history of progressively worsening intracranial hypertension syndrome. The focus is specifically placed on the importance of prompt diagnosis and management to prevent potential life-threatening complications. Minimally invasive modalities, like stereotactic cyst aspiration and neuroendoscopy, are now the preferred techniques of management but present a higher rate of recurrence. Awareness of this condition for early diagnosis and management is fundamental for a better prognosis and patient care.\u0000","PeriodicalId":269581,"journal":{"name":"Edorium Journal of Radiology","volume":"340 3","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140471060","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
Gaucher disease type 3 presenting with deformation of inferior limbs and bone infarction: A case report 以下肢变形和骨梗死为表现的戈歇病3型1例
Edorium Journal of Radiology Pub Date : 2023-08-04 DOI: 10.5348/100024r02za2023cr
Zakaria Abide, Chaimae Es-Sebbani, Amine Cherraqi, A. Haddad, N. Allali, L. Chat
{"title":"Gaucher disease type 3 presenting with deformation of inferior limbs and bone infarction: A case report","authors":"Zakaria Abide, Chaimae Es-Sebbani, Amine Cherraqi, A. Haddad, N. Allali, L. Chat","doi":"10.5348/100024r02za2023cr","DOIUrl":"https://doi.org/10.5348/100024r02za2023cr","url":null,"abstract":"\u0000 Introduction: Gaucher disease (GD) is a lysosomal storage disorder characterized by the accumulation of glucocerebroside in various cells throughout the body. Bone infarction is a common and fearsome complication.\u0000\u0000 Case Report: We present the case of a 5-year-old child diagnosed with Gaucher disease type 3, who exhibited deformation of the inferior limbs and bone pain. Upon evaluation, radiographic examination of the limbs revealed a characteristic triangular appearance of the metaphysis and a serpiginous sclerotic area. A magnetic resonance imaging was performed to confirm the diagnosis of bone infarction.\u0000\u0000 Conclusion: Gaucher disease is a complex genetic disorder. Bone involvement is a significant manifestation causing pain, bone crises, deformities. Various imaging techniques can help for an accurate diagnosis and for a timely intervention and prevention of the disease progression.\u0000","PeriodicalId":269581,"journal":{"name":"Edorium Journal of Radiology","volume":"37 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-08-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"117138875","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
Chilaiditi sign secondary to a right renal agenesis 继发于右肾发育不全
Edorium Journal of Radiology Pub Date : 2022-11-08 DOI: 10.5348/100023r02kb2022cr
K. Berrada, Asaad El Bakkari, H. Jerguigue, R. Latib, Y. Omor
{"title":"Chilaiditi sign secondary to a right renal agenesis","authors":"K. Berrada, Asaad El Bakkari, H. Jerguigue, R. Latib, Y. Omor","doi":"10.5348/100023r02kb2022cr","DOIUrl":"https://doi.org/10.5348/100023r02kb2022cr","url":null,"abstract":"\u0000 Chilaiditi’s sign is a rare radiological finding in which a portion of the colon or small intestine is interposed between the liver and right hemidiaphragm. Associated to pain, it is called Chilaiditi syndrome. We describe the case of a patient who was admitted to our radiology department to release a body-computed tomography (CT) for its breast cancer extension assessment. We incidentally discovered a colic hepato-phrenic interposition related to a Chilaiditi sign associated with right renal agenesis. In this case report we treated Chilaiditi sign can exist without Chilaiditi syndrome, as it could be associated with other pathologies and abnormal anatomic malformation like renal agenesis.\u0000","PeriodicalId":269581,"journal":{"name":"Edorium Journal of Radiology","volume":"20 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"134013224","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
Glutaric aciduria type 1: Typical aspects in imaging 戊二酸尿1型:典型影像学表现
Edorium Journal of Radiology Pub Date : 2022-10-11 DOI: 10.5348/100022r02hz2022cs
Hajar Zebbakh, I. Diallo, N. Lrhorfi, D. Alami, N. Allali, L. Chat
{"title":"Glutaric aciduria type 1: Typical aspects in imaging","authors":"Hajar Zebbakh, I. Diallo, N. Lrhorfi, D. Alami, N. Allali, L. Chat","doi":"10.5348/100022r02hz2022cs","DOIUrl":"https://doi.org/10.5348/100022r02hz2022cs","url":null,"abstract":"\u0000 Glutaric aciduria type 1 is an autosomal recessive lysine and tryptophan disorder characterized by glutamic acid and other metabolic by-product accumulation. This disease can be diagnosed in the postnatal period, supported by magnetic resonance imaging (MRI) and confirmed by biochemistry. This article aims to highlight the typical features of this disease in brain MRI which connects frontotemporal atrophy with bilateral and symmetrical signal abnormalities of the brainstem, periventricular white matter, and basal ganglia. As a result, we use two cases to show how this rare disease manifests itself in imaging.\u0000","PeriodicalId":269581,"journal":{"name":"Edorium Journal of Radiology","volume":"31 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"121962158","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
Meningo-encephalo-vasculitis, optic neuritis, and thrombotic complications: About a fulminant mucormycosis in a diabetic patient 脑膜-脑-血管炎、视神经炎和血栓并发症:关于糖尿病患者的暴发性毛霉病
Edorium Journal of Radiology Pub Date : 2022-06-16 DOI: 10.5348/100020r02io2022cr
Ibtissam El Ouali, Abdeljalil Hamzaoui, Ibrahima Dokal Diallo, M. Fikri, M. Jiddane, F. Touarsa
{"title":"Meningo-encephalo-vasculitis, optic neuritis, and thrombotic complications: About a fulminant mucormycosis in a diabetic patient","authors":"Ibtissam El Ouali, Abdeljalil Hamzaoui, Ibrahima Dokal Diallo, M. Fikri, M. Jiddane, F. Touarsa","doi":"10.5348/100020r02io2022cr","DOIUrl":"https://doi.org/10.5348/100020r02io2022cr","url":null,"abstract":"\u0000 Mucormycosis is a destructive, potentially fatal, and opportunistic fungal infection caused by filamentous Mucorales which commonly affect immunocompromised hosts. This infection might take different forms such as gastrointestinal, pulmonary, cutaneous or even a disseminated form, yet the rhinocerebral localization is historically the primary presentation of the disease and most common type. It originates in the nasal mucosa owing to fungal inoculation, then it spreads through paranasal sinuses and orbits to the brain and its vessels especially the cavernous sinus, leading to thrombotic complications including arterial thrombosis. Herein, we present a case of a 35-year-old male with poorly controlled diabetes who presented with decompensated diabetes, in whom the clinical examination finds subtle signs of orbital cellulitis. The patient subsequently had worsening necrotizing orbital cellulitis which required surgical drainage of the left ethmoid along with large spectrum antibiotic therapy; this was complicated by the development of meningo-encephalo-vasculitis as well as cavernous sinus and left internal carotid thrombosis. Tissue cultures revealed evidence of Rhizopus.\u0000","PeriodicalId":269581,"journal":{"name":"Edorium Journal of Radiology","volume":"52 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-06-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"115127036","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
Neuro-Behçet’s disease revealed by diencephalo-mesencephalic impairment 间脑-中脑损伤所揭示的神经behaperet病
Edorium Journal of Radiology Pub Date : 2022-06-16 DOI: 10.5348/100021r02ja2022cr
Jamal Aouifi, Houda Bouchama, Hajar Eljouadi, A. Hanine
{"title":"Neuro-Behçet’s disease revealed by diencephalo-mesencephalic impairment","authors":"Jamal Aouifi, Houda Bouchama, Hajar Eljouadi, A. Hanine","doi":"10.5348/100021r02ja2022cr","DOIUrl":"https://doi.org/10.5348/100021r02ja2022cr","url":null,"abstract":"\u0000 Introduction: Behçet’s disease is a systemic variable vessel vasculitis with unknown cause. Neurologic involvement known as neuro-Behcet’s disease (NBD) is often diagnosed in patients who present neurological symptoms and radiological lesions of the central nervous system.\u0000\u0000 Case Report: A 42-year-old woman with a history of orogenital ulceration presented with behavioral disorders and heaviness of left hemibody. Brain magnetic resonance imaging (MRI) was performed and showed a pseudo-tumor diencephalo-mesencephalic area with T2 and Flair hypersignal, a slight hypersignal in diffusion sequence, and no contrast uptake.\u0000\u0000 Conclusion: Pseudotumoral NBD is a rare but severe manifestation of Behçet’s disease. Cerebral MRI is the most efficient method to explore, detect, and monitor parenchymal lesions.\u0000","PeriodicalId":269581,"journal":{"name":"Edorium Journal of Radiology","volume":"22 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-06-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"132563931","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
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