发布求助
文献互助 智能选刊 最新文献

Journal of Radiology Case Reports最新文献

筛选
英文 中文
Persistent craniopharyngeal canal with an associated sphenoid sinus fistula. 伴有蝶窦瘘的顽固性颅咽管。
IF 1
Journal of Radiology Case Reports Pub Date : 2023-10-31 eCollection Date: 2023-10-01 DOI: 10.3941/jrcr.v17i8.4707
Chase C Dougherty, Barton F Branstetter
{"title":"Persistent craniopharyngeal canal with an associated sphenoid sinus fistula.","authors":"Chase C Dougherty, Barton F Branstetter","doi":"10.3941/jrcr.v17i8.4707","DOIUrl":"10.3941/jrcr.v17i8.4707","url":null,"abstract":"<p><p>Persistent craniopharyngeal canal (PCC) is a rare congenital anomaly that appears as a linear well-corticated canal running from the sella through the clivus and into the nasopharynx. Case reports of this anomaly have shown it is associated with a range of craniofacial defects, pituitary abnormalities, and meningoencephaloceles. It predisposes patients to bacterial meningitis. In this case a 46-year-old gentleman presenting for preoperative planning for surgical drainage of Potts Puffy tumor was found to have a PCC on CT and MRI. Imaging also demonstrated the presence of chronic inflammation and a fistula extending from the tract into the sphenoid sinus. This unusual presentation of a PCC with a sphenoid sinus fistula broadens the potential clinical presentations of PCC and further emphasizes the ability of this anomaly to serve as a conduit for CNS infection.</p>","PeriodicalId":46520,"journal":{"name":"Journal of Radiology Case Reports","volume":"17 10","pages":"14-20"},"PeriodicalIF":1.0,"publicationDate":"2023-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10852052/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139725680","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
Imaging in hepatopulmonary syndrome-case report. A multicenter approach during the coronavirus pandemic. 肝肺综合征的成像--病例报告。冠状病毒大流行期间的多中心方法。
IF 0.6
Journal of Radiology Case Reports Pub Date : 2023-10-31 eCollection Date: 2023-10-01 DOI: 10.3941/jrcr.v17i8.4411
Afsara Anisa Ahmmed, Randeep Kulshrestha
{"title":"Imaging in hepatopulmonary syndrome-case report. A multicenter approach during the coronavirus pandemic.","authors":"Afsara Anisa Ahmmed, Randeep Kulshrestha","doi":"10.3941/jrcr.v17i8.4411","DOIUrl":"10.3941/jrcr.v17i8.4411","url":null,"abstract":"<p><p>A 60-year-old lady with alcoholic liver disease developed central cyanosis and orthodeoxia. A technetium-99m macro-aggregated albumin lung perfusion scan and contrast echocardiogram were performed. A 13% right to left shunt was calculated from the macro-aggregated albumin scan. There were more bubbles in the left heart than the right at the end of the contrast echocardiogram. Hepatopulmonary syndrome was therefore diagnosed. The patient had a liver transplant five days after these investigations. Further discussion about hepatopulmonary syndrome will be provided. Normally, macro-aggregated albumin scans are performed in few centers, however as this was at the height of the coronavirus pandemic, the scan needed to be performed locally to reduce the chance of the patient getting coronavirus. Local radiographers were remotely instructed on conducting the macro-aggregated albumin scan by a larger center to provide a timely and important investigation in a logistically difficult scenario.</p>","PeriodicalId":46520,"journal":{"name":"Journal of Radiology Case Reports","volume":"17 10","pages":"1-13"},"PeriodicalIF":0.6,"publicationDate":"2023-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10852050/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139725679","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
Breast cancer in a Hispanic patient with Werner syndrome. 一名患有维尔纳综合征的西班牙裔患者的乳腺癌。
IF 1
Journal of Radiology Case Reports Pub Date : 2023-10-31 eCollection Date: 2023-10-01 DOI: 10.3941/jrcr.v17i8.5168
Manuel Menendez Santos, Carlos Gonzalez Baerga, Sanjay Lamsal, Corey Engel, Savas Ozdemir
{"title":"Breast cancer in a Hispanic patient with Werner syndrome.","authors":"Manuel Menendez Santos, Carlos Gonzalez Baerga, Sanjay Lamsal, Corey Engel, Savas Ozdemir","doi":"10.3941/jrcr.v17i8.5168","DOIUrl":"10.3941/jrcr.v17i8.5168","url":null,"abstract":"<p><p>Werner Syndrome is a rare autosomal recessive condition characterized by premature aging and increased risk of malignancies due to gene mutations associated with DNA stability. We present the first case report of a 29-year-old Hispanic female with WS diagnosed with breast cancer. Diagnostic mammography and ultrasound, breast MRI and PET examinations revealed two lesions biopsy proven as invasive ductal carcinoma. The patient underwent neoadjuvant chemotherapy and radical mastectomy. Recurrence occurred 10 months postoperatively with molecular analysis demonstrating TP53 mutations. The multifactorial assessment of breast cancer in this case study is crucial towards optimizing screening, diagnosis and management of this disease in patients with WS.</p>","PeriodicalId":46520,"journal":{"name":"Journal of Radiology Case Reports","volume":"17 10","pages":"21-31"},"PeriodicalIF":1.0,"publicationDate":"2023-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10852053/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139724468","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
Preoperative Transcatheter Arterial Embolization for Spontaneous Rupture of Huge Amebic Liver Abscess with Massive Intraperitoneal Hemorrhage 经导管动脉栓塞治疗阿米巴肝脓肿自发性破裂伴大量腹腔内出血
Journal of Radiology Case Reports Pub Date : 2023-10-11 DOI: 10.3941/jrcr.v17i8.4837
None Koesbandono, Raditya Utomo, Benyamin Lukito, Jusef Treser, Nyoman Aditya Sindunata
{"title":"Preoperative Transcatheter Arterial Embolization for Spontaneous Rupture of Huge Amebic Liver Abscess with Massive Intraperitoneal Hemorrhage","authors":"None Koesbandono, Raditya Utomo, Benyamin Lukito, Jusef Treser, Nyoman Aditya Sindunata","doi":"10.3941/jrcr.v17i8.4837","DOIUrl":"https://doi.org/10.3941/jrcr.v17i8.4837","url":null,"abstract":"An 18-year-old male developed a huge liver abscess with severe anemia over the course of 2 weeks. Abdominal contrast enhanced computed tomography showed ruptured huge liver abscess in the right liver lobe with signs of active hemorrhage (contrast extravasation). Serology examination confirmed amoeba as the suspected pathogen of cause. Angiography was performed followed by transcatheter arterial embolization to localize and control the hemorrhage. Embolization using a combination of polyvinyl alcohol and gelfoam successfully controlled the active hemorrhage. Exploratory laparotomy was performed to evacuate and debride the huge abscess. Metronidazole was given and showed good results. Huge liver abscess size is a predictor of conservative management failure and requires a gradual step-up intervention. The purpose of this paper is to explain the importance of imaging in detecting liver abscess and active hemorrhage along with the role of interventional radiology in this case.","PeriodicalId":46520,"journal":{"name":"Journal of Radiology Case Reports","volume":"2014 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136213559","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
Flood Syndrome: Endovascular management of spontaneous rupture of an umbilical hernia due to long-standing ascites – A case report 洪水综合征:血管内处理因长期腹水引起的脐疝自发性破裂-一例报告
Journal of Radiology Case Reports Pub Date : 2023-10-11 DOI: 10.3941/jrcr.v17i8.4884
Pablo Peñalver Calero, Marco Leyva Vásquez-Caicedo, Claudia Jimena González-Nieto, Javier Eduardo Armijo Astrain, José Vicente Méndez Montero
{"title":"Flood Syndrome: Endovascular management of spontaneous rupture of an umbilical hernia due to long-standing ascites – A case report","authors":"Pablo Peñalver Calero, Marco Leyva Vásquez-Caicedo, Claudia Jimena González-Nieto, Javier Eduardo Armijo Astrain, José Vicente Méndez Montero","doi":"10.3941/jrcr.v17i8.4884","DOIUrl":"https://doi.org/10.3941/jrcr.v17i8.4884","url":null,"abstract":"Umbilical hernias are common in patients with cirrhosis of the liver and ascites; however, spontaneous rupture of the hernia is a rare complication. Flood Syndrome occurs very rarely in cirrhotic patients with massive ascites and refers to the spontaneous rupture of an umbilical hernia followed by leakage of ascites fluid. A literature search shows that patients have been managed both operatively and nonoperatively for this condition. We report a case of a 56-year-old man with a history of alcohol-related liver cirrhosis and massive ascites refractory to medical therapy with sudden and spontaneous perforation of his hernia leading to drainage of ascitic fluid from the abdomen. We performed a transjugular intrahepatic portosystematic shunt to relieve portal pressure and subsequent intraabdominal pressure. The patient had resolution of symptoms and the ascitic fluid outflow was resolved.","PeriodicalId":46520,"journal":{"name":"Journal of Radiology Case Reports","volume":"50 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136213252","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
Descending necrotizing mediastinitis secondary to retropharyngeal abscess 降性坏死性纵隔炎继发于咽后脓肿
Journal of Radiology Case Reports Pub Date : 2023-10-11 DOI: 10.3941/jrcr.v17i8.5095
Sarah M Nwia, Christian D Huebner, Jeremy B. Nguyen
{"title":"Descending necrotizing mediastinitis secondary to retropharyngeal abscess","authors":"Sarah M Nwia, Christian D Huebner, Jeremy B. Nguyen","doi":"10.3941/jrcr.v17i8.5095","DOIUrl":"https://doi.org/10.3941/jrcr.v17i8.5095","url":null,"abstract":"We report a case of descending necrotizing mediastinitis (DNM) in a 68-year-old male who presented in acute respiratory distress accompanied with anterior cervical neck swelling and pain with swallowing. Contrast enhanced computed tomography (CECT) of the neck demonstrated a large, peripherally enhancing retropharyngeal fluid and air collection that appeared to communicate with a fluid and air collection within the mediastinum. CECT of the chest demonstrated punctate foci of air and fat stranding along the anterior and superior mediastinum. Radiological evidence and the presence of necrosis on surgical debridement of the retropharyngeal abscess established the diagnosis of DNM. This case emphasizes the role of computed tomography (CT) in the diagnosis of DNM and demonstrates the utility of chest imaging in a high-risk patient who presents with a retropharyngeal abscess.","PeriodicalId":46520,"journal":{"name":"Journal of Radiology Case Reports","volume":"104 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136213255","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
Trigeminal Lipomatosis: A Rare Cause of Intractable Neuralgia 三叉神经脂肪瘤病:难治性神经痛的罕见病因
Journal of Radiology Case Reports Pub Date : 2023-10-11 DOI: 10.3941/jrcr.v17i8.4709
Apoorva Sehgal, Jyoti Kumar, Ishwar Singh, Ashish Gopal
{"title":"Trigeminal Lipomatosis: A Rare Cause of Intractable Neuralgia","authors":"Apoorva Sehgal, Jyoti Kumar, Ishwar Singh, Ashish Gopal","doi":"10.3941/jrcr.v17i8.4709","DOIUrl":"https://doi.org/10.3941/jrcr.v17i8.4709","url":null,"abstract":"Lipomatosis of nerve, earlier known as fibrolipomatous hamartoma is a rare condition which predominantly affects peripheral nerves, cranial nerve involvement being extremely uncommon. Preoperative consideration of this entity is of paramount importance as its inadvertent complete surgical resection may inevitably result in significant neurological deficit. We report a case of trigeminal lipomatosis in a young patient with trigeminal neuralgia.","PeriodicalId":46520,"journal":{"name":"Journal of Radiology Case Reports","volume":"12 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136213557","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
Zinner’s Syndrome: Case report of a Developmental Anomaly of the Mesonephric Duct 津纳综合征:中肾管发育异常1例报告
Journal of Radiology Case Reports Pub Date : 2023-10-10 DOI: 10.3941/jrcr.v17i8.5055
Mirco Cleva, Luca Montaldo, Giovanna Graziani, Ennio Bruschi, Massimo Valentino
{"title":"Zinner’s Syndrome: Case report of a Developmental Anomaly of the Mesonephric Duct","authors":"Mirco Cleva, Luca Montaldo, Giovanna Graziani, Ennio Bruschi, Massimo Valentino","doi":"10.3941/jrcr.v17i8.5055","DOIUrl":"https://doi.org/10.3941/jrcr.v17i8.5055","url":null,"abstract":"Zinner’s syndrome is a rare congenital malformation characterized by the association of unilateral renal agenesis with ipsilateral seminal vesicle cyst and ejaculatory duct obstruction. Most patients are asymptomatic until the third or fourth decade of life when the syndrome is associated with dysuria, perineal pain, infertility, and painful ejaculation. In this report, we present the common imaging findings of this rare developmental anomaly involving the mesonephric duct in a 48-year-old male patient experiencing pelvic pain, recurrent dysuria, and pollakiuria.","PeriodicalId":46520,"journal":{"name":"Journal of Radiology Case Reports","volume":"89 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136357814","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
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 : 2023-09-01 DOI: 10.3941/jrcr.v17i9.4873
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.v17i9.4873","DOIUrl":"https://doi.org/10.3941/jrcr.v17i9.4873","url":null,"abstract":"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.","PeriodicalId":46520,"journal":{"name":"Journal of Radiology Case Reports","volume":"82 1","pages":"1-14"},"PeriodicalIF":1.0,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139347070","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
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 : 2023-09-01 DOI: 10.3941/jrcr.v17i9.4774
W. 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":"W. Wakeford, Dimitrios Ioannidis","doi":"10.3941/jrcr.v17i9.4774","DOIUrl":"https://doi.org/10.3941/jrcr.v17i9.4774","url":null,"abstract":"Introduction 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. Presentation of case 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. Discussion 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. Conclusion 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.","PeriodicalId":46520,"journal":{"name":"Journal of Radiology Case Reports","volume":"92 1","pages":"29-33"},"PeriodicalIF":1.0,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139344533","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
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：604180095
Book学术官方微信