Journal of Radiology Case Reports最新文献

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Pericardial hydatid cyst: The water lily sign as a classical sign in a nonclassical location. 心包水瘤囊肿:睡莲征作为非典型位置的经典征象。
IF 1
Journal of Radiology Case Reports Pub Date : 2023-09-01 DOI: 10.3941/jrcr.v17i9.5152
Israa Alsulami, Reem Alwasiah, Mohammed Alsalman, Abdulmohsen Alyousef
{"title":"Pericardial hydatid cyst: The water lily sign as a classical sign in a nonclassical location.","authors":"Israa Alsulami, Reem Alwasiah, Mohammed Alsalman, Abdulmohsen Alyousef","doi":"10.3941/jrcr.v17i9.5152","DOIUrl":"https://doi.org/10.3941/jrcr.v17i9.5152","url":null,"abstract":"Hydatid disease is a parasitic infection that usually targets the liver and is rarely seen affecting the heart. Herein, we present an incidentally diagnosed cardiac hydatid cyst with a pathognomonic radiological feature of a water lily sign.","PeriodicalId":46520,"journal":{"name":"Journal of Radiology Case Reports","volume":"14 1","pages":"15-21"},"PeriodicalIF":1.0,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139343525","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
Coil embolization of a fistula from the right inferior phrenic artery to the right pulmonary artery with involvement of further arteries: A rare case report. 右下膈动脉至右肺动脉瘘管的线圈栓塞术,同时累及其他动脉:罕见病例报告。
IF 1
Journal of Radiology Case Reports Pub Date : 2023-09-01 DOI: 10.3941/jrcr.v17i9.4972
L. J. Juergens, A. Thalhammer, T. Gruber-Rouh, V. Koch, T. J. Vogl, S. S. Martin
{"title":"Coil embolization of a fistula from the right inferior phrenic artery to the right pulmonary artery with involvement of further arteries: A rare case report.","authors":"L. J. Juergens, A. Thalhammer, T. Gruber-Rouh, V. Koch, T. J. Vogl, S. S. Martin","doi":"10.3941/jrcr.v17i9.4972","DOIUrl":"https://doi.org/10.3941/jrcr.v17i9.4972","url":null,"abstract":"A 51-year-old female patient was presenting dyspnea for more than a year with no previous lung infections or surgery. Initially, a diagnostic computed tomography was made, showing a rare arterio-arterial malformation between the right inferior phrenic and right pulmonary artery leading into a vascular bundle in the middle lung lobe. Due to the patients' dyspnea and massive extent of malformation, the indication for transcatheter arterial embolization was made. The first transcatheter arterial embolization procedure involved the inferior phrenic and a selective branch of the internal thoracic artery. Interventional angiography as well as computed tomography revealed further extend of the malformation showing a connection of right lateral thoracic, hepatic, and inferior epigastric artery to the fistula. After one month, a second transcatheter arterial embolization of these arteries as well as a second approach of the proximal internal thoracic artery was performed. In the follow-up the patient described a substantial improvement of her dyspnea and showed no signs of infections. A phrenic artery to pulmonary artery fistula is an extremely rare case occurring congenital or acquired. Patients may be asymptomatic or present, among others, dyspnea, hemoptysis, pulmonary infections and congestive heart failure. Symptomatic patients require treatment using transcatheter arterial embolization or surgical resection. The patient had dyspnea and a substantial extent of malformation with possibly complicated clinical course. The recommended less invasive treatment using transcatheter arterial embolization was successfully performed. In conclusion, our patient represented a rare congenital case of systemic and pulmonary artery communication, which we were able to treat sufficiently with coil embolization.","PeriodicalId":46520,"journal":{"name":"Journal of Radiology Case Reports","volume":"46 1","pages":"22-28"},"PeriodicalIF":1.0,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139345008","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 embolization with EVOH for the treatment of a Rasmussen aneurysm. EVOH血管内栓塞治疗拉斯穆森动脉瘤。
IF 1
Journal of Radiology Case Reports Pub Date : 2023-08-31 eCollection Date: 2023-08-01 DOI: 10.3941/jrcr.v17i8.4687
Kirollos Bechay, Michael David Katz, Brian Quinn
{"title":"Endovascular embolization with EVOH for the treatment of a Rasmussen aneurysm.","authors":"Kirollos Bechay, Michael David Katz, Brian Quinn","doi":"10.3941/jrcr.v17i8.4687","DOIUrl":"10.3941/jrcr.v17i8.4687","url":null,"abstract":"<p><p>First-line treatment of pulmonary artery aneurysms/pseudoaneurysms (PAA/PAPA) is percutaneous or endovascular embolization. The present case of a Rasmussen aneurysm, a PAPA caused by Tuberculosis (TB), was successfully treated with ethylene-vinyl alcohol (EVOH), a radiopaque liquid embolic agent with favorable characteristics. A 35-year-old man presented as a new patient with hemoptysis, and CT imaging revealed multiple cavitary lesions and a 2.1 cm aneurysm in the upper right lobe. Endovascular treatment was delivered and a complete lack of filling of the lesion was noted on post-treatment angiography. The patient's history includes risk factors and past TB infection. Despite the suspicious imaging, diagnostic tests were negative for active TB in this patient. He was then found to have MRSA bacteremia and a mediastinal lymph node positive for M. avium. The etiology of this aneurysm is suspicious for the superinfection of a chronic tuberculous cavity with M. avium, MRSA, or both.</p>","PeriodicalId":46520,"journal":{"name":"Journal of Radiology Case Reports","volume":"17 8","pages":"8-14"},"PeriodicalIF":1.0,"publicationDate":"2023-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10435256/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10145769","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
Traditional Chinese Acupuncture Causing Acute Hemoperitoneum from Direct Liver Injury. 中医针灸对直接肝损伤急性腹血的影响。
IF 1
Journal of Radiology Case Reports Pub Date : 2023-08-31 eCollection Date: 2023-08-01 DOI: 10.3941/jrcr.v17i8.5100
Edward Zhenyu Seah
{"title":"Traditional Chinese Acupuncture Causing Acute Hemoperitoneum from Direct Liver Injury.","authors":"Edward Zhenyu Seah","doi":"10.3941/jrcr.v17i8.5100","DOIUrl":"10.3941/jrcr.v17i8.5100","url":null,"abstract":"<p><p>Traditional Chinese medicine is a popular form of complementary and/or alternative medicine in Southeast Asia, often incorporating acupuncture. Acupuncture involves the insertion of thin needles into varied anatomical points on the body for the relief of a range of symptoms, such as musculoskeletal aches and pains. We present the first reported case of percutaneous liver injury secondary to acupuncture. We aim to familiarize readers with this rare and as-yet unreported case of intra-abdominal injury related to acupuncture, which is commonly practiced in many countries in Eastern and Southeast Asia.</p>","PeriodicalId":46520,"journal":{"name":"Journal of Radiology Case Reports","volume":"17 8","pages":"15-20"},"PeriodicalIF":1.0,"publicationDate":"2023-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10435255/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10145775","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
Complication of barbotage, acute calcific bursitis treated successfully. 手术并发症,急性钙化滑囊炎治疗成功。
IF 1
Journal of Radiology Case Reports Pub Date : 2023-08-31 eCollection Date: 2023-08-01 DOI: 10.3941/jrcr.v17i8.4603
Cem Gokhan, Sagar Maheshwari, Harish Nagraj, Sofia Vrizidou, Thulasi Tharmalingam
{"title":"Complication of barbotage, acute calcific bursitis treated successfully.","authors":"Cem Gokhan, Sagar Maheshwari, Harish Nagraj, Sofia Vrizidou, Thulasi Tharmalingam","doi":"10.3941/jrcr.v17i8.4603","DOIUrl":"10.3941/jrcr.v17i8.4603","url":null,"abstract":"<p><p>One of the most common causes of chronic shoulder pain that significantly impairs patients' quality of life is rotator cuff calcific tendinitis. The supportive approach of analgesics, anti-inflammatory medications, and physiotherapy is preferred to treat mild symptoms. However, severe intractable symptoms necessitate alternative treatment, and ultrasonography-guided percutaneous barbotage is regarded as an effective treatment technique due to its minimal invasiveness, low cost, and rapid significant pain relief. Post-barbotage complications are reported as acute calcific bursitis along with infection, bleeding, and tendon rupture. In our case, a 41-year-old female presented with a substantial amount of pain shortly after barbotage, which was diagnosed as acute calcific bursitis, a complication of the procedure. Subacromial-subdeltoid steroid injection was used successfully to treat this condition.</p>","PeriodicalId":46520,"journal":{"name":"Journal of Radiology Case Reports","volume":"17 8","pages":"1-7"},"PeriodicalIF":1.0,"publicationDate":"2023-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10435257/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10127571","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
Coil embolization of a fistula from the right inferior phrenic artery to the right pulmonary artery with involvement of further arteries: A rare case report. 右下膈动脉至右肺动脉瘘管的线圈栓塞术,同时累及其他动脉:罕见病例报告。
IF 1
Journal of Radiology Case Reports Pub Date : 2023-08-01 eCollection Date: 2023-09-01 DOI: 10.3941/jrcr.v17i8.4972
L J Juergens, A Thalhammer, T Gruber-Rouh, V Koch, T J Vogl, S S Martin
{"title":"Coil embolization of a fistula from the right inferior phrenic artery to the right pulmonary artery with involvement of further arteries: A rare case report.","authors":"L J Juergens, A Thalhammer, T Gruber-Rouh, V Koch, T J Vogl, S S Martin","doi":"10.3941/jrcr.v17i8.4972","DOIUrl":"https://doi.org/10.3941/jrcr.v17i8.4972","url":null,"abstract":"<p><p>A 51-year-old female patient was presenting dyspnea for more than a year with no previous lung infections or surgery. Initially, a diagnostic computed tomography was made, showing a rare arterio-arterial malformation between the right inferior phrenic and right pulmonary artery leading into a vascular bundle in the middle lung lobe. Due to the patients' dyspnea and massive extent of malformation, the indication for transcatheter arterial embolization was made. The first transcatheter arterial embolization procedure involved the inferior phrenic and a selective branch of the internal thoracic artery. Interventional angiography as well as computed tomography revealed further extend of the malformation showing a connection of right lateral thoracic, hepatic, and inferior epigastric artery to the fistula. After one month, a second transcatheter arterial embolization of these arteries as well as a second approach of the proximal internal thoracic artery was performed. In the follow-up the patient described a substantial improvement of her dyspnea and showed no signs of infections. A phrenic artery to pulmonary artery fistula is an extremely rare case occurring congenital or acquired. Patients may be asymptomatic or present, among others, dyspnea, hemoptysis, pulmonary infections and congestive heart failure. Symptomatic patients require treatment using transcatheter arterial embolization or surgical resection. The patient had dyspnea and a substantial extent of malformation with possibly complicated clinical course. The recommended less invasive treatment using transcatheter arterial embolization was successfully performed. In conclusion, our patient represented a rare congenital case of systemic and pulmonary artery communication, which we were able to treat sufficiently with coil embolization.</p>","PeriodicalId":46520,"journal":{"name":"Journal of Radiology Case Reports","volume":"17 9","pages":"22-28"},"PeriodicalIF":1.0,"publicationDate":"2023-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10718308/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138812190","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
Nasal obstruction in a 14 year old girl caused by a huge middle turbinate mucocele appearing radiologically as an inverted papilloma. 一名 14 岁女孩因巨大的中鼻甲粘液瘤引起鼻塞,放射学表现为倒置乳头状瘤。
IF 1
Journal of Radiology Case Reports Pub Date : 2023-08-01 eCollection Date: 2023-09-01 DOI: 10.3941/jrcr.v17i8.4774
William Wakeford, Dimitrios Ioannidis
{"title":"Nasal obstruction in a 14 year old girl caused by a huge middle turbinate mucocele appearing radiologically as an inverted papilloma.","authors":"William Wakeford, Dimitrios Ioannidis","doi":"10.3941/jrcr.v17i8.4774","DOIUrl":"https://doi.org/10.3941/jrcr.v17i8.4774","url":null,"abstract":"<p><strong>Introduction: </strong>We present a case of a fourteen year old girl who presented with a large intra-nasal mass to the ENT team at a district general hospital in the UK.</p><p><strong>Presentation of case: </strong>The girl presented predominantly with nasal obstruction and some symptoms of allergic rhinitis. Imaging revealed a large lesion abutting the skull base and causing bony remodelling with marked septal deviation. Based both on CT and MRI imaging, the reporting (non-head and neck) radiologist suggested inverted papilloma as a differential diagnosis. Intra-operative exploration in fact revealed a very large left middle turbinate mucocele extending to the left frontal sinus. The mass was excised endoscopically without complications.</p><p><strong>Discussion: </strong>Although concha bullosa of the middle turbinate of the nose are common, development of a mucocele within them is far less common and for such a mucocele to develop to this size in a child is extremely rare. The egg shell lining of the lesion can be a tell-tale sign of their aetiology when taken alongside other radiological factors. This case highlights challenges in radiological diagnosis of intra-nasal masses in children, which can lead to delays and increased anxiety.</p><p><strong>Conclusion: </strong>When assessing nasal masses in children it is important to keep a wide differential due to the challenges of diagnosis. A close conversation should be had with local head and neck radiologists and, of course, where there is a unilateral nasal mass tissue sampling is essential and may be taken as part of a full excision where clinically indicated.</p>","PeriodicalId":46520,"journal":{"name":"Journal of Radiology Case Reports","volume":"17 9","pages":"29-33"},"PeriodicalIF":1.0,"publicationDate":"2023-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10718309/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138812193","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
Pericardial hydatid cyst: The water lily sign as a classical sign in a nonclassical location. 心包水瘤囊肿:睡莲征作为非典型位置的经典征象。
IF 1
Journal of Radiology Case Reports Pub Date : 2023-08-01 eCollection Date: 2023-09-01 DOI: 10.3941/jrcr.v17i8.5152
Israa Alsulami, Reem Alwasiah, Mohammed Alsalman, Abdulmohsen Alyousef
{"title":"Pericardial hydatid cyst: The water lily sign as a classical sign in a nonclassical location.","authors":"Israa Alsulami, Reem Alwasiah, Mohammed Alsalman, Abdulmohsen Alyousef","doi":"10.3941/jrcr.v17i8.5152","DOIUrl":"https://doi.org/10.3941/jrcr.v17i8.5152","url":null,"abstract":"<p><p>Hydatid disease is a parasitic infection that usually targets the liver and is rarely seen affecting the heart. Herein, we present an incidentally diagnosed cardiac hydatid cyst with a pathognomonic radiological feature of a water lily sign.</p>","PeriodicalId":46520,"journal":{"name":"Journal of Radiology Case Reports","volume":"17 9","pages":"15-21"},"PeriodicalIF":1.0,"publicationDate":"2023-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10718310/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138812194","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
Rosai-Dorfman Disease in a Pediatric Patient: Imaging Findings and Pathology with a brief review of the Literature. 一名儿科患者的罗赛-多夫曼病:影像学检查结果和病理学,以及文献简评。
IF 1
Journal of Radiology Case Reports Pub Date : 2023-08-01 eCollection Date: 2023-09-01 DOI: 10.3941/jrcr.v17i8.4873
Thomas Hartmann, Nadia Solomon, Gabriel Lerner, Lauren Ehrlich
{"title":"Rosai-Dorfman Disease in a Pediatric Patient: Imaging Findings and Pathology with a brief review of the Literature.","authors":"Thomas Hartmann, Nadia Solomon, Gabriel Lerner, Lauren Ehrlich","doi":"10.3941/jrcr.v17i8.4873","DOIUrl":"https://doi.org/10.3941/jrcr.v17i8.4873","url":null,"abstract":"<p><p>Rosai-Dorfman Disease, otherwise known as sinus histiocytosis with massive lymphadenopathy, is a rare form of non-Langerhans cell histiocytosis with an estimated incidence of 100 cases per year in the United States. Due to its variable presentation and nonspecific clinical findings, it is particularly difficult to diagnose in pediatric patients. We report a case of an 11-month-old male who presented with a 4-day history of a right groin mass. Ultrasound of the groin and pelvis demonstrated, and MRI of the abdomen and pelvis confirmed an inguinal mass with surrounding lymphadenopathy. Pathology confirmed Rosai-Dorfman Disease and the patient improved after starting oral steroid therapy. To the best of our knowledge, this is the first case of Rosai-Dorfman Disease involving the inguinal region in an infant under 1 year of age reported in the literature. In this case report, we discuss the imaging and histology findings as well as provide a brief literature review for this diagnosis.</p>","PeriodicalId":46520,"journal":{"name":"Journal of Radiology Case Reports","volume":"17 9","pages":"1-14"},"PeriodicalIF":1.0,"publicationDate":"2023-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10718311/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138812195","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
Tumour induced osteopenia due to phosphaturic mesenchymal sinonasal tumour presenting with delayed onset insufficiency fractures. 肿瘤诱导的骨质减少是由于磷酸-间充质鼻窦肿瘤表现为迟发性功能不全性骨折。
IF 1
Journal of Radiology Case Reports Pub Date : 2023-07-31 eCollection Date: 2023-07-01 DOI: 10.3941/jrcr.v17i7.4912
Freda Jawan, Weiling Lim, Joe Francis
{"title":"Tumour induced osteopenia due to phosphaturic mesenchymal sinonasal tumour presenting with delayed onset insufficiency fractures.","authors":"Freda Jawan,&nbsp;Weiling Lim,&nbsp;Joe Francis","doi":"10.3941/jrcr.v17i7.4912","DOIUrl":"10.3941/jrcr.v17i7.4912","url":null,"abstract":"<p><p>We present a case of a 48-year-old female who presented with epistaxis. Magnetic resonance imaging (MRI) revealed a mass within the left nasal cavity which was revealed to be a phosphaturic mesenchymal sinonasal tumour. The patient defaulted treatment at this stage and later re-presented with pelvic and groin pain for which plain radiographs and computed tomography (CT) scan demonstrated diffuse osteopenia and multiple pelvic fractures of varying ages. MRI of the pelvis and both thighs revealed abnormal marrow signal of the bones and confirmed the presence of pelvic fractures. Multiple pseudo-fractures were seen at both femurs and scapula. The radiological findings along with abnormal biochemical markers were attributed to the paraneoplastic entity of tumour induced osteomalacia, in the context of unresected phosphaturic mesenchymal tumour. The tumour was resected, and patient showed complete reversal of the associated biochemical abnormalities. This case exemplifies that with early identification and complete resection of the causative tumour, the prognosis is excellent.</p>","PeriodicalId":46520,"journal":{"name":"Journal of Radiology Case Reports","volume":"17 7","pages":"8-16"},"PeriodicalIF":1.0,"publicationDate":"2023-07-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10435251/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10052720","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
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