首页 > 最新文献

Case Reports in Radiology最新文献

英文 中文
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。
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

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.

硬纤维瘤是一种局部侵袭性肿瘤,即使切除后复发率也很高。经皮冷冻消融是一种有效的替代治疗方法,相关风险较小。患者年龄50岁,有导管原位癌病史,双侧乳房切除术和硅胶植入后的状态,左乳房可触及肿块,核心活检证实植入物下方为硬纤维瘤。患者在六个月内接受了两次冷冻消融手术。在这两种方法中,部分种植体被包括在消融区,对种植体没有任何负面影响。冷冻消融是一种可行的治疗方案,以硬纤维瘤毗邻硅胶乳房植入物。
{"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":" ","pages":"2650790"},"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。
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

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.

脊索样胶质瘤是一种罕见的肿瘤实体。到目前为止,全球只有大约90例病例被描述。脊索样胶质瘤包括起源于第三脑室前部的低级别鞍上神经上皮肿瘤,在MRI上具有一致的放射学特征。该病变应被视为第三脑室肿瘤的鉴别诊断。本文中描述的患者非常独特,尽管只切除了部分肿瘤,但在几年的随访中,残余肿瘤没有进展。术前对这种疾病实体的认识对于修改治疗方法和改善患者预后至关重要。
{"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":" ","pages":"3584837"},"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。
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

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.

右心逆位是一种罕见的先天性畸形,其特征是心尖位于右侧,腹部内脏器官反向旋转。我们报告一个不寻常的病例右心与位置反转在一个59岁的男子,转介盆腔超声扫描,因为下尿路阻塞的症状和相当正常的前列腺特异性抗原(PSA)值。诊断为前列腺肿大,中叶突出,尿量明显残留,需要检查肾脏是否有肾积水,导致偶然发现倒位。经进一步调查,诊断为右心逆位。医生应该注意这种异常,主要是因为它可能与其他疾病有关,如原发性纤毛运动障碍,因此提供适当的干预措施以降低发病率和死亡率。
{"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":" ","pages":"7107293"},"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。
Pub Date : 2019-11-11 eCollection Date: 2019-01-01 DOI: 10.1155/2019/6545472
Mahdis Solhjoo, Supreeya Swarup, Amgad N Makaryus

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.

我们提出一个病例广泛主动脉夹层(AD)确定在一个妇女的非典型症状。经胸超声心动图(TTE)可以识别多个位置的内膜皮瓣,从而快速诊断和治疗。在大多数情况下,CT血管造影是诊断AD的首选成像方式。TTE快速、准确,可用于肾衰竭。我们的病例强调了床边超声心动图在AD诊断中的重要作用,特别是在具有典型症状的患者中,AD的诊断可能不被接受,实际上会导致负面和可能致命的后果。
{"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":" ","pages":"6545472"},"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
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
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.
一位28岁的男性,有多肺动静脉畸形线圈栓塞史,在首次栓塞11年后出现咯血。左上叶空腔病变,伴螺旋变形和毛玻璃影,被认为是咯血的原因。行支气管动脉栓塞术。
{"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":"87 1","pages":""},"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
Pub Date : 2019-10-13 DOI: 10.1155/2019/2016959
M. Petullà, G. Mazzarella, L. Critelli, L. Paone, D. Laganà
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.
螺旋主动脉是主动脉正常解剖路线的一种变体。这种罕见的情况以主动脉明显扭曲为特征。根据我们的经验,它涉及肾下主动脉道,这是一种不寻常的情况,因为在文献中没有其他病例。其特征是至少存在两个扭结,并且在它们之间插入一个卷绕。它是通过血管ct诊断的,其反应是偶然的,从无症状的临床角度来看。
{"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":"38 1","pages":""},"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
Pub Date : 2019-07-08 DOI: 10.1155/2019/6734816
M. Herskowitz, J. Walsh, M. Lilly, K. McFarland
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.
经导管血管造影和栓塞术一直被认为是治疗钝性骨盆创伤后血流动力学不稳定的金标准。虽然通常根据术前ct血管造影的外渗分布可以很容易地定位出血源,但在评估异常解剖结构时应谨慎。一种起源于髂外动脉腹壁下支的变异闭孔动脉通常被称为尸冠动脉。我们提出一个钝性骨盆创伤的情况下,病人表现出外渗在两个髂内动脉的前分布。在双侧髂内动脉栓塞后,确定和栓塞双侧尸冠分支对于实现该患者的血流动力学稳定至关重要。
{"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":"17 1","pages":""},"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
Pub Date : 2019-07-03 DOI: 10.1155/2019/6156948
Lauren E Watchmaker, J. Watchmaker, G. Watchmaker
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.
无症状的显著冠状动脉疾病(CAD)患者有发生包括心肌梗死(MI)在内的意外心脏事件的风险。实验室研究、压力测试和冠状动脉成像(包括冠状动脉钙(CAC)评分)评估高危人群。手部和腕部x光片显示明显的动脉壁钙化可能为识别有心脏事件风险的无症状个体提供额外的手段。在此,我们报告了一系列没有已知心脏疾病的患者,在评估其手部状况的x线片中显示桡动脉和/或尺动脉有明显的钙沉积。每个系列患者随后发现冠状动脉成像有钙化,未来心脏事件的风险增加。我们的研究表明,放射科医生和手部专家观察到的外周动脉钙化可能需要对身体其他部位的动脉粥样硬化进行系统评估。
{"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":"55 1","pages":""},"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
Pub Date : 2019-07-01 DOI: 10.1155/2019/3067346
Naoki Kunitomo, H. Fujii, A. Fujita, Yumiko Hamano, Minako Takanosawa, H. Sugimoto
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.
甲状腺舌管癌是一种罕见的恶性肿瘤,起源于甲状腺组织或舌管壁的残余,通常发生在舌管的解剖过程中。起源于舌骨的TGD癌非常罕见,但由于TGD在极少数情况下穿透舌骨,因此也可能发生。本报告描述的情况下,30岁的男子TGD癌起源于舌骨。计算机断层扫描显示舌骨肿块扩大了舌骨皮质骨。肿块中心为实性钙化,边缘为囊性。当我们遇到舌骨钙化肿块时,我们应该考虑鉴别诊断中的TGD癌。
{"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":"85 1","pages":""},"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
Description of Two Cases of Anaplastic Large Cell Lymphoma Associated with a Breast Implant. 两例与乳房植入物相关的间变性大细胞淋巴瘤的描述。
Pub Date : 2019-06-27 eCollection Date: 2019-01-01 DOI: 10.1155/2019/6137198
Julie Crèvecoeur, Véronique Jossa, Joan Somja, Jean-Claude Parmentier, Jean-Luc Nizet, André Crèvecoeur

Breast implant-associated anaplastic large cell lymphoma (BIA-ALCL) is a recently recognized provisional entity in the 2017 revision of the World Health Organization classification of lymphoid neoplasms. Although the majority of the cases described in the literature demonstrate an effusion confined to the capsule of the breast implant, this rare pathology can also invade the capsule and adjacent tissues and/or involve lymph nodes. We hereby report two new cases of BIA-ALCL in a 58-year-old and a 47-year-old Caucasian female who received a silicone breast implant. The first patient showed a sudden and rapid right breast volume increase 6 years after the implantation surgery. As for the second patient, a left breast volume increase was observed also suddenly and quickly 11 years after surgery. In both cases, an uncompressed mammography was performed allowing a new approach to highlight periprosthetic fluid reaction. Pathologic examination of the fluid collection revealed atypical cells positive for CD30 and CD45 and negative for ALK and CK7. This allowed pathologists to diagnose a breast implant-associated anaplastic large cell lymphoma. Patients were treated with bilateral capsulectomy with no additional local or systemic therapy. The development of breast augmentation may come with an increase in the frequency of this pathology. Radiologists and senologists must therefore be careful when women with breast implants show an increase of breast volume and all cases of BIA-ALCL must be recorded and reported.

乳房植入物相关间变性大细胞淋巴瘤(BIA-ALCL)是世界卫生组织2017年修订的淋巴肿瘤分类中最近认可的临时实体。尽管文献中描述的大多数病例显示积液局限于乳房植入物的包膜,但这种罕见的病理学也可能侵犯包膜和邻近组织和/或涉及淋巴结。我们在此报告两例新的BIA-ALCL病例,一名58岁和一名47岁的白人女性接受了硅胶乳房植入术。第一位患者在植入手术后6年,右乳房体积突然快速增加。至于第二名患者,在手术后11年,左乳房体积也突然迅速增加。在这两种情况下,都进行了未压缩的乳房X光检查,从而采用了一种新的方法来突出假体周围的液体反应。液体采集的病理学检查显示非典型细胞CD30和CD45阳性,ALK和CK7阴性。这使病理学家能够诊断出与乳房植入物相关的间变性大细胞淋巴瘤。患者接受双侧晶状体囊切除术治疗,无需额外的局部或全身治疗。隆胸的发展可能伴随着这种病理的频率增加。因此,当植入乳房的女性乳房体积增加时,放射科医生和Senologist必须小心,并且必须记录和报告所有BIA-ALCL病例。
{"title":"Description of Two Cases of Anaplastic Large Cell Lymphoma Associated with a Breast Implant.","authors":"Julie Crèvecoeur,&nbsp;Véronique Jossa,&nbsp;Joan Somja,&nbsp;Jean-Claude Parmentier,&nbsp;Jean-Luc Nizet,&nbsp;André Crèvecoeur","doi":"10.1155/2019/6137198","DOIUrl":"https://doi.org/10.1155/2019/6137198","url":null,"abstract":"<p><p>Breast implant-associated anaplastic large cell lymphoma (BIA-ALCL) is a recently recognized provisional entity in the 2017 revision of the World Health Organization classification of lymphoid neoplasms. Although the majority of the cases described in the literature demonstrate an effusion confined to the capsule of the breast implant, this rare pathology can also invade the capsule and adjacent tissues and/or involve lymph nodes. We hereby report two new cases of BIA-ALCL in a 58-year-old and a 47-year-old Caucasian female who received a silicone breast implant. The first patient showed a sudden and rapid right breast volume increase 6 years after the implantation surgery. As for the second patient, a left breast volume increase was observed also suddenly and quickly 11 years after surgery. In both cases, an uncompressed mammography was performed allowing a new approach to highlight periprosthetic fluid reaction. Pathologic examination of the fluid collection revealed atypical cells positive for CD30 and CD45 and negative for ALK and CK7. This allowed pathologists to diagnose a breast implant-associated anaplastic large cell lymphoma. Patients were treated with bilateral capsulectomy with no additional local or systemic therapy. The development of breast augmentation may come with an increase in the frequency of this pathology. Radiologists and senologists must therefore be careful when women with breast implants show an increase of breast volume and all cases of BIA-ALCL must be recorded and reported.</p>","PeriodicalId":30326,"journal":{"name":"Case Reports in Radiology","volume":"2019 ","pages":"6137198"},"PeriodicalIF":0.0,"publicationDate":"2019-06-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2019/6137198","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41214681","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
期刊
Case Reports in Radiology
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
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
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1