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Headache and MRI Changes after Endovascular Treatment of a Cerebral Aneurysm. 脑动脉瘤血管内治疗后头痛及MRI改变。
Case Reports in Radiology Pub Date : 2019-12-20 eCollection Date: 2019-01-01 DOI: 10.1155/2019/6917902
Liv Jorunn Høllesli, Martin W Kurz, Gry Inger N Behzadi, Tore Solbakken, Svein Harald Mørkve, Kathinka D Kurz
{"title":"Headache and MRI Changes after Endovascular Treatment of a Cerebral Aneurysm.","authors":"Liv Jorunn Høllesli,&nbsp;Martin W Kurz,&nbsp;Gry Inger N Behzadi,&nbsp;Tore Solbakken,&nbsp;Svein Harald Mørkve,&nbsp;Kathinka D Kurz","doi":"10.1155/2019/6917902","DOIUrl":"https://doi.org/10.1155/2019/6917902","url":null,"abstract":"<p><strong>Background: </strong>The main complications after endovascular therapy of intracranial aneurysms are aneurysm rupture and thromboembolic events. Yet, the widespread use of magnetic resonance imaging (MRI) in follow-up of these patients also demonstrates other, rarely known complications such as aseptic meningitis and foreign body reaction.</p><p><strong>Case presentation: </strong>A small aneurysm in the right posterior communicating artery was treated with endovascular therapy in a 65 year old woman. Two weeks after successful interventional treatment, the patient developed a headache. On MRI performed five months after intervention, vasogenic edema was seen in the vascular territory of the right internal carotid artery. The edema and the symptoms diminished without specific treatment within a year.</p><p><strong>Interpretation: </strong>The clinical and radiological presentation of this case are suggestive of a foreign body reaction, a treatable condition that radiologists and clinicians should be aware of.</p>","PeriodicalId":30326,"journal":{"name":"Case Reports in Radiology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2019-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2019/6917902","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37536910","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: 1
Cryoablation of a Symptomatic Chest Wall Desmoid Tumor Underneath a Silicone Breast Implant. 硅胶乳房植入物下有症状的胸壁硬纤维瘤的冷冻消融。
Case Reports in Radiology Pub Date : 2019-12-18 eCollection Date: 2019-01-01 DOI: 10.1155/2019/2650790
Siddhant S Kulkarni, Amy R Deipolyi, Yolanda C D Bryce, Joseph P Erinjeri
{"title":"Cryoablation of a Symptomatic Chest Wall Desmoid Tumor Underneath a Silicone Breast Implant.","authors":"Siddhant S Kulkarni,&nbsp;Amy R Deipolyi,&nbsp;Yolanda C D Bryce,&nbsp;Joseph P Erinjeri","doi":"10.1155/2019/2650790","DOIUrl":"https://doi.org/10.1155/2019/2650790","url":null,"abstract":"<p><p>Desmoid tumors are locally aggressive tumors that have a high rate of reoccurrence, even after resection. Percutaneous cryoablation is an effective alternative treatment with less associated risk. A patient in the fifth decade of life with a history of ductal carcinoma-in-situ, status post bilateral mastectomy and silicone implant placement, presented with a palpable mass in the left breast, core biopsy proven to be a desmoid tumor underneath the implant. The patient underwent two cryoablation procedures in a six-month period. During both procedures part of the implant was included in the ablation zone without any negative effects on the implant. Cryoablation is a feasible treatment option for desmoid tumors adjacent to silicone breast implants.</p>","PeriodicalId":30326,"journal":{"name":"Case Reports in Radiology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2019-12-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2019/2650790","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37536909","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: 1
Chordoid Glioma as a Differential Diagnosis of Anterior Third Ventricle Tumours: A Rare Case Report and Five-Year Follow-Up. 脊索样胶质瘤作为前第三脑室肿瘤的鉴别诊断:一罕见病例报告及五年随访。
Case Reports in Radiology Pub Date : 2019-12-04 eCollection Date: 2019-01-01 DOI: 10.1155/2019/3584837
Kristin Suetens, Jeroen Swinnen, Linde Stessens, Sofie Van Cauter, Geert Gelin
{"title":"Chordoid Glioma as a Differential Diagnosis of Anterior Third Ventricle Tumours: A Rare Case Report and Five-Year Follow-Up.","authors":"Kristin Suetens,&nbsp;Jeroen Swinnen,&nbsp;Linde Stessens,&nbsp;Sofie Van Cauter,&nbsp;Geert Gelin","doi":"10.1155/2019/3584837","DOIUrl":"https://doi.org/10.1155/2019/3584837","url":null,"abstract":"<p><p>Chordoid glioma is a rare and relatively recently defined tumour entity. Worldwide there have only been around 90 cases described until now. A chordoid glioma comprises a low-grade suprasellar neuroepithelial neoplasm originating in the anterior part of the third ventricle, with consistent radiological features on MRI. This lesion should be considered as a differential of third ventricle tumours. The patient described in this paper is quite unique in the sense that despite only partial tumour resection was obtained, the residual tumour was not progressive during several years of follow-up. Preoperative recognition of this disease entity is crucial to modify the treatment approach and improve patient outcome.</p>","PeriodicalId":30326,"journal":{"name":"Case Reports in Radiology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2019-12-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2019/3584837","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37486955","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: 4
Incidental Finding of Dextrocardia with Situs Inversus in a 59-Year-Old Man. 一个59岁男性偶然发现右位心性倒置。
Case Reports in Radiology Pub Date : 2019-12-01 eCollection Date: 2019-01-01 DOI: 10.1155/2019/7107293
Emmanuel Kobina Mesi Edzie, Klenam Dzefi-Tettey, Obed Cudjoe, Philip Narteh Gorleku, Patrick Adu
{"title":"Incidental Finding of Dextrocardia with Situs Inversus in a 59-Year-Old Man.","authors":"Emmanuel Kobina Mesi Edzie,&nbsp;Klenam Dzefi-Tettey,&nbsp;Obed Cudjoe,&nbsp;Philip Narteh Gorleku,&nbsp;Patrick Adu","doi":"10.1155/2019/7107293","DOIUrl":"https://doi.org/10.1155/2019/7107293","url":null,"abstract":"<p><p>Dextrocardia with situs inversus is a rare congenital anomaly, which is characterized by right-sided heart apex and inversely rotated visceral organs of the abdomen. We report an unusual case of dextrocardia with situs inversus in a 59-year-old man, referred for a pelvic ultrasound scan because of symptoms of lower urinary tract obstruction and after a fairly normal prostate specific antigen (PSA) value. A diagnosis of enlarged prostate gland with a prominent median lobe and significant residual urine volume was made, which necessitated the examination of the kidneys for hydronephrosis, resulting in the incidental finding of situs inversus. On further investigation, the diagnosis of dextrocardia with situs inversus was made. Physicians should look out for this anomaly primarily because it may be associated with other conditions like primary ciliary dyskinesia so appropriate interventions are offered to reduce morbidities and mortality.</p>","PeriodicalId":30326,"journal":{"name":"Case Reports in Radiology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2019-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2019/7107293","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37499598","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: 5
A Case of Aortic Dissection Presenting with Atypical Symptoms and Diagnosed with Transthoracic Echocardiography. 以非典型症状表现的主动脉夹层1例经胸超声心动图诊断。
Case Reports in Radiology Pub Date : 2019-11-11 eCollection Date: 2019-01-01 DOI: 10.1155/2019/6545472
Mahdis Solhjoo, Supreeya Swarup, Amgad N Makaryus
{"title":"A Case of Aortic Dissection Presenting with Atypical Symptoms and Diagnosed with Transthoracic Echocardiography.","authors":"Mahdis Solhjoo,&nbsp;Supreeya Swarup,&nbsp;Amgad N Makaryus","doi":"10.1155/2019/6545472","DOIUrl":"https://doi.org/10.1155/2019/6545472","url":null,"abstract":"<p><p>We present a case of an extensive aortic dissection (AD) identified in a woman with atypical symptoms. Transthoracic echocardiography (TTE) allowed the identification of an intimal flap in multiple locations and resulted in rapid diagnosis and treatment. In most cases, CT angiography is the imaging modality of choice for diagnosis of AD. TTE is rapid and accurate and can be used in kidney failure. Our case highlights the important role of bedside echocardiography in the diagnosis of AD, especially in the patient with a typical symptoms in whom this diagnosis of AD may not be entertained and actually missed leading to negative and possibly deadly consequences.</p>","PeriodicalId":30326,"journal":{"name":"Case Reports in Radiology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2019-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2019/6545472","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37449722","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: 5
Hemoptysis due to Pulmonary Arteriovenous Malformation after Coil Embolization during Long-Term Follow-Up 线圈栓塞后肺动静脉畸形咯血的长期随访
Case Reports in Radiology Pub Date : 2019-10-20 DOI: 10.1155/2019/4506253
M. Shimohira, K. Iwata, K. Ohta, Y. Sawada, Takeshi Hashimoto, K. Okuda, R. Nakanishi, Y. Shibamoto
{"title":"Hemoptysis due to Pulmonary Arteriovenous Malformation after Coil Embolization during Long-Term Follow-Up","authors":"M. Shimohira, K. Iwata, K. Ohta, Y. Sawada, Takeshi Hashimoto, K. Okuda, R. Nakanishi, Y. Shibamoto","doi":"10.1155/2019/4506253","DOIUrl":"https://doi.org/10.1155/2019/4506253","url":null,"abstract":"A 28-year-old man with a history of coil embolization of multiple pulmonary arteriovenous malformations presented with hemoptysis 11 years after initial embolization. A cavity lesion in the left upper lobe, which was accompanied by deformed coils and ground-glass opacity, was considered responsible for hemoptysis. Embolization of the bronchial artery was performed.","PeriodicalId":30326,"journal":{"name":"Case Reports in Radiology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2019-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74121003","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: 3
Incidental Diagnosis of a Rare Case of Corkscrew Aorta 1例罕见的螺旋状主动脉的偶然诊断
Case Reports in Radiology Pub Date : 2019-10-13 DOI: 10.1155/2019/2016959
M. Petullà, G. Mazzarella, L. Critelli, L. Paone, D. Laganà
{"title":"Incidental Diagnosis of a Rare Case of Corkscrew Aorta","authors":"M. Petullà, G. Mazzarella, L. Critelli, L. Paone, D. Laganà","doi":"10.1155/2019/2016959","DOIUrl":"https://doi.org/10.1155/2019/2016959","url":null,"abstract":"The corkscrew aorta is a variant of the normal anatomical course of the aorta. This rare condition is characterized by a marked tortuosity of the aorta. In our experience it concerns the tract of subrenal aorta, that is an unusual condition, since there are no other cases in the literature. It is characterized by the presence of at least two kinking, and a coiling interposed among them. It is diagnosed by Angio-CT and its response is incidental, being from an asymptomatic clinical point of view.","PeriodicalId":30326,"journal":{"name":"Case Reports in Radiology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2019-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"81004773","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: 1
Importance of Both Internal and External Iliac Artery Interrogation in Pelvic Trauma as Evidenced by Hemorrhage from Bilateral Corona Mortis with Unilateral Aberrant Origin off the External Iliac Artery 骨盆外伤中髂内外动脉检查的重要性:双侧尸冠出血伴单侧髂外动脉异常
Case Reports in Radiology Pub Date : 2019-07-08 DOI: 10.1155/2019/6734816
M. Herskowitz, J. Walsh, M. Lilly, K. McFarland
{"title":"Importance of Both Internal and External Iliac Artery Interrogation in Pelvic Trauma as Evidenced by Hemorrhage from Bilateral Corona Mortis with Unilateral Aberrant Origin off the External Iliac Artery","authors":"M. Herskowitz, J. Walsh, M. Lilly, K. McFarland","doi":"10.1155/2019/6734816","DOIUrl":"https://doi.org/10.1155/2019/6734816","url":null,"abstract":"Transcatheter angiography and embolization has long been recognized as the gold standard for patients with hemodynamic instability secondary to blunt pelvic trauma. While often the bleeding source can be readily localized based on the distribution of extravasation on preprocedural Computed Tomographic Angiography, one should be cautious in assessment for aberrant anatomy. A variant obturator artery originating from the inferior epigastric branch of the external iliac artery is commonly referred to as the corona mortis. We present a case of blunt pelvic trauma in which a patient demonstrated extravasation in the anterior distributions of both internal iliac arteries. Following embolization of bilateral internal iliac arteries, identification and embolization of bilateral corona mortis branches was crucial to achieving hemodynamic stability in this patient.","PeriodicalId":30326,"journal":{"name":"Case Reports in Radiology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2019-07-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75888998","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: 5
Arterial Calcification on Wrist Radiographs May Suggest Need for Evaluation of Atherosclerosis in Asymptomatic Individuals 腕部x线片上动脉钙化可能提示需要对无症状个体进行动脉粥样硬化评估
Case Reports in Radiology Pub Date : 2019-07-03 DOI: 10.1155/2019/6156948
Lauren E Watchmaker, J. Watchmaker, G. Watchmaker
{"title":"Arterial Calcification on Wrist Radiographs May Suggest Need for Evaluation of Atherosclerosis in Asymptomatic Individuals","authors":"Lauren E Watchmaker, J. Watchmaker, G. Watchmaker","doi":"10.1155/2019/6156948","DOIUrl":"https://doi.org/10.1155/2019/6156948","url":null,"abstract":"Asymptomatic individuals with significant coronary artery disease (CAD) are at risk for unanticipated cardiac events including myocardial infarction (MI). Laboratory studies, stress tests, and coronary artery imaging including coronary artery calcium (CAC) scoring evaluate at-risk individuals. Hand and wrist x-rays demonstrating significant arterial wall calcification may provide an additional means to identify asymptomatic individuals at risk for cardiac events. Here we report a case series of patients without known cardiac disease who demonstrated significant calcium deposits in the radial and/or ulnar arteries in radiographs performed for evaluation of their hand conditions. Each series patient was subsequently found to have calcification on coronary artery imaging and an elevated risk of future cardiac events. Our series suggests that peripheral arterial calcifications observed by radiologists and hand specialists may warrant systemic evaluation for atherosclerosis in other areas of the body.","PeriodicalId":30326,"journal":{"name":"Case Reports in Radiology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2019-07-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82776040","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: 4
Thyroglossal Duct Carcinoma Originating in the Hyoid Bone 甲状腺舌导管癌起源于舌骨
Case Reports in Radiology Pub Date : 2019-07-01 DOI: 10.1155/2019/3067346
Naoki Kunitomo, H. Fujii, A. Fujita, Yumiko Hamano, Minako Takanosawa, H. Sugimoto
{"title":"Thyroglossal Duct Carcinoma Originating in the Hyoid Bone","authors":"Naoki Kunitomo, H. Fujii, A. Fujita, Yumiko Hamano, Minako Takanosawa, H. Sugimoto","doi":"10.1155/2019/3067346","DOIUrl":"https://doi.org/10.1155/2019/3067346","url":null,"abstract":"Thyroglossal duct (TGD) carcinoma is a rare malignant tumor arising from remnants of thyroid tissue or the wall of the duct and generally occurs along the anatomic course of the TGD. TGD carcinoma originating in the hyoid bone is extremely rare but can occur since the TGD penetrates the hyoid bone on rare occasions. This report describes the case of a 30-year-old man with TGD carcinoma originating in the hyoid bone. Computed tomography demonstrated a mass in the hyoid bone that expanded the cortical bone of the hyoid. The mass had a central solid component with calcification and a marginal cystic component. When we encounter a calcified mass in the hyoid bone, we should consider TGD carcinoma among the differential diagnoses.","PeriodicalId":30326,"journal":{"name":"Case Reports in Radiology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2019-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78144389","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: 3
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