首页 > 最新文献

Journal of Radiology Case Reports最新文献

英文 中文
Acute Hemorrhagic Cholecystitis with Large Hemoperitoneum: Treatment with Microcoil Embolization and Subsequent Cholecystectomy. 急性出血性胆囊炎伴大腹膜出血:微线圈栓塞治疗及后续胆囊切除术。
IF 1 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2021-02-28 eCollection Date: 2021-02-01 DOI: 10.3941/jrcr.v15i2.3901
Don Nguyen, J Scott Goodwin, Nirjhor Bhowmik, Guillaume Boiteau, Jonathan Potts

Hemorrhagic cholecystitis is a potentially deadly and difficult to recognize entity. It is associated with cystic artery pseudoaneurysm and is usually seen in the setting of acute calculous cholecystitis. We report two cases of hemorrhagic cholecystitis with arteriographic findings of cystic artery pseudoaneurysms that were successfully embolized using microcoils, facilitating subsequent cholecystectomy. Both cases had unusual presentations of gallbladder rupture with hemoperitoneum, the latter of which was atypical occurring in the absence of gallstones. We believe when hemorrhagic cholecystitis is suspected, a two-step therapeutic approach should be employed with embolization of the bleeding cystic artery followed by cholecystectomy. A comprehensive literature review and discussion of hemorrhagic cholecystitis will be provided.

出血性胆囊炎是一种潜在的致命且难以识别的疾病。它与囊性动脉假性动脉瘤有关,通常见于急性结石性胆囊炎。我们报告两例出血性胆囊炎的动脉造影发现囊性动脉假性动脉瘤,成功栓塞微线圈,促进后续胆囊切除术。这两个病例都有不寻常的表现胆囊破裂并腹腔积血,后者是不典型的,在没有胆结石的情况下发生。我们认为,当怀疑出血性胆囊炎时,应采用两步治疗方法,首先栓塞出血的囊性动脉,然后进行胆囊切除术。本文将对出血性胆囊炎进行全面的文献回顾和讨论。
{"title":"Acute Hemorrhagic Cholecystitis with Large Hemoperitoneum: Treatment with Microcoil Embolization and Subsequent Cholecystectomy.","authors":"Don Nguyen,&nbsp;J Scott Goodwin,&nbsp;Nirjhor Bhowmik,&nbsp;Guillaume Boiteau,&nbsp;Jonathan Potts","doi":"10.3941/jrcr.v15i2.3901","DOIUrl":"https://doi.org/10.3941/jrcr.v15i2.3901","url":null,"abstract":"<p><p>Hemorrhagic cholecystitis is a potentially deadly and difficult to recognize entity. It is associated with cystic artery pseudoaneurysm and is usually seen in the setting of acute calculous cholecystitis. We report two cases of hemorrhagic cholecystitis with arteriographic findings of cystic artery pseudoaneurysms that were successfully embolized using microcoils, facilitating subsequent cholecystectomy. Both cases had unusual presentations of gallbladder rupture with hemoperitoneum, the latter of which was atypical occurring in the absence of gallstones. We believe when hemorrhagic cholecystitis is suspected, a two-step therapeutic approach should be employed with embolization of the bleeding cystic artery followed by cholecystectomy. A comprehensive literature review and discussion of hemorrhagic cholecystitis will be provided.</p>","PeriodicalId":46520,"journal":{"name":"Journal of Radiology Case Reports","volume":"15 2","pages":"25-34"},"PeriodicalIF":1.0,"publicationDate":"2021-02-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7942966/pdf/jrcr-15-2-25.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25486773","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
Vigabatrin-associated Reversible MRI Abnormalities in an Infant with Tuberous Sclerosis. 婴儿结节性硬化症维加巴林相关的可逆性MRI异常。
IF 1 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2021-02-28 eCollection Date: 2021-02-01 DOI: 10.3941/jrcr.v15i2.3918
Joseph Franklin Craft, Agustin M Cardenas

Vigabatrin therapy is commonly used in infants diagnosed with tuberous sclerosis complex, particularly in the setting of epilepsy. Utilization of vigabatrin can result in bilateral and symmetric abnormal sequence changes within the deep brain matter and brainstem on magnetic resonance imaging. These abnormalities occur predominantly in infancy, are reversible, and can be asymptomatic or result in symptomatic clinical manifestations. We present a case with classic neuroimaging findings. Familiarity with these findings can prevent unnecessary follow up tests or studies and the cost of continuing or discontinuing vigabatrin therapy should be weighed heavily against the potential manifestation of extrapyramidal symptoms.

维加巴林治疗通常用于诊断为结节性硬化症的婴儿,特别是癫痫患者。使用维加巴林可在磁共振成像上引起脑深部物质和脑干内双侧和对称的异常序列改变。这些异常主要发生在婴儿期,是可逆的,可以无症状或导致症状性临床表现。我们提出一个典型的神经影像学发现的病例。熟悉这些发现可以防止不必要的随访试验或研究,继续或停止维他汀治疗的费用应与锥体外系症状的潜在表现进行重大权衡。
{"title":"Vigabatrin-associated Reversible MRI Abnormalities in an Infant with Tuberous Sclerosis.","authors":"Joseph Franklin Craft,&nbsp;Agustin M Cardenas","doi":"10.3941/jrcr.v15i2.3918","DOIUrl":"https://doi.org/10.3941/jrcr.v15i2.3918","url":null,"abstract":"<p><p>Vigabatrin therapy is commonly used in infants diagnosed with tuberous sclerosis complex, particularly in the setting of epilepsy. Utilization of vigabatrin can result in bilateral and symmetric abnormal sequence changes within the deep brain matter and brainstem on magnetic resonance imaging. These abnormalities occur predominantly in infancy, are reversible, and can be asymptomatic or result in symptomatic clinical manifestations. We present a case with classic neuroimaging findings. Familiarity with these findings can prevent unnecessary follow up tests or studies and the cost of continuing or discontinuing vigabatrin therapy should be weighed heavily against the potential manifestation of extrapyramidal symptoms.</p>","PeriodicalId":46520,"journal":{"name":"Journal of Radiology Case Reports","volume":"15 2","pages":"1-6"},"PeriodicalIF":1.0,"publicationDate":"2021-02-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7942967/pdf/jrcr-15-2-1.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25486771","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
Magnetic Resonance Imaging Appearance of Erythema Nodosum: A Case Report. 结节性红斑的磁共振影像表现1例。
IF 1 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2021-01-31 eCollection Date: 2021-01-01 DOI: 10.3941/jrcr.v15i1.3919
Ankita Chauhan, Richard Thomas

Erythema nodosum (EN) is the commonest inflammation of the subcutaneous fat tissue (panniculitis). Erythema nodosum (EN) requires an interdisciplinary approach and exclusion of all underlying causes. We present a case of an 18-year-old female with a history of recurrent streptococcal infections over the years, who developed pain and swelling in the left ankle. To evaluate the persistent ankle swelling, the physician ordered a magnetic resonance imaging (MRI) of the left lower extremity. The MRI appearance of EN has not been described in detail in the literature so far.

结节性红斑(EN)是最常见的皮下脂肪组织炎症(泛膜炎)。结节性红斑(EN)需要跨学科的方法和排除所有潜在的原因。我们报告一例18岁的女性,多年来有复发性链球菌感染史,左脚踝疼痛和肿胀。为了评估持续的踝关节肿胀,医生要求对左下肢进行磁共振成像(MRI)检查。迄今为止,文献尚未详细描述EN的MRI表现。
{"title":"Magnetic Resonance Imaging Appearance of Erythema Nodosum: A Case Report.","authors":"Ankita Chauhan,&nbsp;Richard Thomas","doi":"10.3941/jrcr.v15i1.3919","DOIUrl":"https://doi.org/10.3941/jrcr.v15i1.3919","url":null,"abstract":"<p><p>Erythema nodosum (EN) is the commonest inflammation of the subcutaneous fat tissue (panniculitis). Erythema nodosum (EN) requires an interdisciplinary approach and exclusion of all underlying causes. We present a case of an 18-year-old female with a history of recurrent streptococcal infections over the years, who developed pain and swelling in the left ankle. To evaluate the persistent ankle swelling, the physician ordered a magnetic resonance imaging (MRI) of the left lower extremity. The MRI appearance of EN has not been described in detail in the literature so far.</p>","PeriodicalId":46520,"journal":{"name":"Journal of Radiology Case Reports","volume":"15 1","pages":"21-29"},"PeriodicalIF":1.0,"publicationDate":"2021-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7942961/pdf/jrcr-15-1-21.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25486769","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
Pancreatic Neuroendocrine Tumor presenting as a diffuse pancreatic enlargement, case report and review of literature. 胰腺神经内分泌肿瘤表现为弥漫性胰腺增大,病例报告及文献复习。
IF 1 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2021-01-31 eCollection Date: 2021-01-01 DOI: 10.3941/jrcr.v15i1.3822
Faeze Salahshour, Reza Taslimi, Najme-Sadat Moosavi, Niloofar Ayoobi Yazdi, Mohsen Esfandbod

Pancreatic neuroendocrine tumors are rare neoplasms that comprise 1-2% of all pancreatic tumors. However, they are the second most common solid pancreatic neoplasms. They have a wide range of imaging appearances and they can show common to very rare imaging presentations. Most of the time they are solitary well-marginated enhancing solid mass arising in a certain aspect of the pancreas. We present a case report of a 41-year-old female who underwent clinical work-up for abdominal pain, loss of appetite and weight loss for the past year. Ultrasound, computed tomography, and magnetic resonance imaging show diffuse homogenous pancreatic enlargement without contour deformity or a focal mass. Lymphoma and autoimmune pancreatitis were suggested based on imaging findings but IGg4 level and other lab data were normal. Endoscopic ultrasonography confirmed the diffuse enlargement of the pancreas without peripheral structures involvement. The pathological results of multiple fine-needle aspiration biopsy from all parts of the enlarged pancreas revealed a low-grade neuroendocrine tumor.

胰腺神经内分泌肿瘤是一种罕见的肿瘤,占所有胰腺肿瘤的1-2%。然而,它们是第二常见的实体性胰腺肿瘤。它们有广泛的影像学表现,它们可以表现出常见到非常罕见的影像学表现。大多数情况下,它们是孤立的,边缘良好的增强实性肿块,出现在胰腺的某个部位。我们提出一个41岁的女性病例报告,她在过去的一年里因腹痛、食欲不振和体重减轻而接受了临床检查。超声、计算机断层和磁共振成像显示胰腺弥漫性均匀增大,无轮廓畸形或局灶性肿块。影像学结果提示淋巴瘤和自身免疫性胰腺炎,但IGg4水平和其他实验室数据正常。内窥镜超声检查证实胰腺弥漫性扩大,未累及周围结构。胰腺肿大部位多次细针穿刺活检病理结果显示为低度神经内分泌肿瘤。
{"title":"Pancreatic Neuroendocrine Tumor presenting as a diffuse pancreatic enlargement, case report and review of literature.","authors":"Faeze Salahshour,&nbsp;Reza Taslimi,&nbsp;Najme-Sadat Moosavi,&nbsp;Niloofar Ayoobi Yazdi,&nbsp;Mohsen Esfandbod","doi":"10.3941/jrcr.v15i1.3822","DOIUrl":"https://doi.org/10.3941/jrcr.v15i1.3822","url":null,"abstract":"<p><p>Pancreatic neuroendocrine tumors are rare neoplasms that comprise 1-2% of all pancreatic tumors. However, they are the second most common solid pancreatic neoplasms. They have a wide range of imaging appearances and they can show common to very rare imaging presentations. Most of the time they are solitary well-marginated enhancing solid mass arising in a certain aspect of the pancreas. We present a case report of a 41-year-old female who underwent clinical work-up for abdominal pain, loss of appetite and weight loss for the past year. Ultrasound, computed tomography, and magnetic resonance imaging show diffuse homogenous pancreatic enlargement without contour deformity or a focal mass. Lymphoma and autoimmune pancreatitis were suggested based on imaging findings but IGg4 level and other lab data were normal. Endoscopic ultrasonography confirmed the diffuse enlargement of the pancreas without peripheral structures involvement. The pathological results of multiple fine-needle aspiration biopsy from all parts of the enlarged pancreas revealed a low-grade neuroendocrine tumor.</p>","PeriodicalId":46520,"journal":{"name":"Journal of Radiology Case Reports","volume":"15 1","pages":"11-20"},"PeriodicalIF":1.0,"publicationDate":"2021-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7942962/pdf/jrcr-15-1-11.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25486768","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: 6
Honoring our helpers. 向我们的帮手致敬。
IF 1 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2021-01-31 eCollection Date: 2021-01-01 DOI: 10.3941/jrcr.v15i1.4273
Roland Talanow, Frederik Giesel

This special issue of the Journal of Radiology Case Reports honors the reviewers who donated their time and expertise throughout the year 2020 to the high quality and success of this journal.

本期《放射学病例报告杂志》特刊向在2020年全年为该杂志的高质量和成功贡献时间和专业知识的审稿人致敬。
{"title":"Honoring our helpers.","authors":"Roland Talanow,&nbsp;Frederik Giesel","doi":"10.3941/jrcr.v15i1.4273","DOIUrl":"https://doi.org/10.3941/jrcr.v15i1.4273","url":null,"abstract":"<p><p>This special issue of the Journal of Radiology Case Reports honors the reviewers who donated their time and expertise throughout the year 2020 to the high quality and success of this journal.</p>","PeriodicalId":46520,"journal":{"name":"Journal of Radiology Case Reports","volume":"15 1","pages":"30-32"},"PeriodicalIF":1.0,"publicationDate":"2021-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7942963/pdf/jrcr-15-1-30.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25486770","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
An Infratemporal Meningioma: A Diagnostic Dilemma. 颞下脑膜瘤:诊断困境。
IF 1 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2021-01-31 eCollection Date: 2021-01-01 DOI: 10.3941/jrcr.v15i1.3898
Arlinder Kaur, Rofiah Ali, Effat Omar, Hilwati Hashim

A 46-year-old male presented with painless, recurrent bilateral ear discharge and an enlarging right temporal swelling. There were no neurological deficits. Imaging revealed an enhancing, soft tissue mass at the right infratemporal region involving the right temporalis muscle with a small, enhancing intradural component and associated hyperostosis of the greater wing of the right sphenoid bone. Tumour debulking of the right temporalis tumour was performed. Tumour invasion of the right temporalis muscle was noted intraoperatively. Histopathological result was consistent with fibrous meningioma WHO Grade 1 involving surgical resection margins. Follow-up MRI revealed residual right temporal extracranial component. Thus, plans were made for a second stage tumour debulking, however at time of writing, surgery had not been performed. This case highlights the differing appearances of the common meningioma occurring extracranially with elaboration of its differential diagnosis and management.

46岁男性,表现为无痛性,复发性双耳分泌物和右侧颞肿胀。没有神经功能缺陷。影像学显示右侧颞下区软组织肿块增强,累及右侧颞肌,伴一小块增强的硬膜内成分,伴右侧蝶骨大翼骨质增生。对右侧颞部肿瘤进行肿瘤清除。术中发现肿瘤侵犯右颞肌。组织病理学结果与WHO 1级纤维脑膜瘤一致,涉及手术切除边缘。后续MRI显示右侧颞颅外成分残留。因此,制定了第二阶段肿瘤切除的计划,但在撰写本文时,尚未进行手术。本病例强调了发生在颅外的普通脑膜瘤的不同表现,并阐述了其鉴别诊断和治疗。
{"title":"An Infratemporal Meningioma: A Diagnostic Dilemma.","authors":"Arlinder Kaur,&nbsp;Rofiah Ali,&nbsp;Effat Omar,&nbsp;Hilwati Hashim","doi":"10.3941/jrcr.v15i1.3898","DOIUrl":"https://doi.org/10.3941/jrcr.v15i1.3898","url":null,"abstract":"<p><p>A 46-year-old male presented with painless, recurrent bilateral ear discharge and an enlarging right temporal swelling. There were no neurological deficits. Imaging revealed an enhancing, soft tissue mass at the right infratemporal region involving the right temporalis muscle with a small, enhancing intradural component and associated hyperostosis of the greater wing of the right sphenoid bone. Tumour debulking of the right temporalis tumour was performed. Tumour invasion of the right temporalis muscle was noted intraoperatively. Histopathological result was consistent with fibrous meningioma WHO Grade 1 involving surgical resection margins. Follow-up MRI revealed residual right temporal extracranial component. Thus, plans were made for a second stage tumour debulking, however at time of writing, surgery had not been performed. This case highlights the differing appearances of the common meningioma occurring extracranially with elaboration of its differential diagnosis and management.</p>","PeriodicalId":46520,"journal":{"name":"Journal of Radiology Case Reports","volume":"15 1","pages":"1-10"},"PeriodicalIF":1.0,"publicationDate":"2021-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7942964/pdf/jrcr-15-1-1.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25486767","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
Extramedullary Plasmacytoma of the breast in a patient with Multiple Myeloma. 多发性骨髓瘤患者的乳腺髓外浆细胞瘤。
IF 1 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2020-12-31 eCollection Date: 2020-12-01 DOI: 10.3941/jrcr.v14i12.4110
Stephen Vong, Shannon Marisa Navarro, Morgan Darrow, Shadi Aminololama-Shakeri

Extramedullary plasmacytoma of the breast is rare. It is important to recognize the imaging findings and include it as a differential consideration in multiple myeloma patients with a breast mass. A 74-year-old woman undergoing chemotherapy for relapsed multiple myeloma presented with a palpable mass in her right breast. A screening mammogram four months prior was unremarkable. She underwent a diagnostic right mammogram which showed two well-circumscribed hyperdense masses. An ultrasound of the right breast showed mixed echogenic masses with indistinct margins and increased vascularity. Ultrasound guided biopsy confirmed the presence of an extramedullary plasmacytoma. A follow-up whole body PET/CT demonstrated an FDG-avid right breast mass with extensive osseous metastases.

乳腺髓外浆细胞瘤是罕见的。重要的是要认识到影像学表现,并将其作为多发性骨髓瘤患者乳腺肿块的鉴别考虑。一名74岁女性,因复发性多发性骨髓瘤接受化疗,右乳房出现可触及的肿块。4个月前的乳房x光检查结果没有显著差异。她接受了诊断性乳房x光检查,显示两个界限清楚的高密度肿块。右乳超声显示混合性回声肿块,边界不清,血管增多。超声引导活检证实髓外浆细胞瘤的存在。随后的全身PET/CT显示右侧乳腺肿块伴广泛骨转移。
{"title":"Extramedullary Plasmacytoma of the breast in a patient with Multiple Myeloma.","authors":"Stephen Vong,&nbsp;Shannon Marisa Navarro,&nbsp;Morgan Darrow,&nbsp;Shadi Aminololama-Shakeri","doi":"10.3941/jrcr.v14i12.4110","DOIUrl":"https://doi.org/10.3941/jrcr.v14i12.4110","url":null,"abstract":"<p><p>Extramedullary plasmacytoma of the breast is rare. It is important to recognize the imaging findings and include it as a differential consideration in multiple myeloma patients with a breast mass. A 74-year-old woman undergoing chemotherapy for relapsed multiple myeloma presented with a palpable mass in her right breast. A screening mammogram four months prior was unremarkable. She underwent a diagnostic right mammogram which showed two well-circumscribed hyperdense masses. An ultrasound of the right breast showed mixed echogenic masses with indistinct margins and increased vascularity. Ultrasound guided biopsy confirmed the presence of an extramedullary plasmacytoma. A follow-up whole body PET/CT demonstrated an FDG-avid right breast mass with extensive osseous metastases.</p>","PeriodicalId":46520,"journal":{"name":"Journal of Radiology Case Reports","volume":"14 12","pages":"14-23"},"PeriodicalIF":1.0,"publicationDate":"2020-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943045/pdf/jrcr-14-12-14.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25476887","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: 2
Penile Mondor's disease: Imaging in two cases. 阴茎蒙多氏病:2例影像学分析。
IF 1 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2020-12-31 eCollection Date: 2020-12-01 DOI: 10.3941/jrcr.v14i12.3926
Michele Foresti, Andrea Parmiggiani

Penile Mondor's disease is a rare and under-recognized benign genital condition consisting of an isolated thrombosis of the dorsal superficial vein of the penis. Symptoms do not show distinctive features and there are asymptomatic cases. The patients usually present with a cord-like induration at dorsum of the penis. Diagnosis is usually made based on history and physical examination. The role of imaging in Mondor's disease is to identify the intravascular thrombus. In case of diagnostic uncertainty, Grey scale and Doppler ultrasound can be useful to detect the extent of thrombosis demonstrating echogenic material within venous lumen, vessel incompressibility and absence of flow, as well as painful selective pressure. The use of Magnetic Resonance imaging is controversial and not used routinely. Usually treatment is conservative: sexual rest, local anesthetics, anti-inflammatories, antibiotics in case of infection and anticoagulants. Sclerosing lymphangitis and Peyronie's disease have been described as possible differential diagnosis.

阴茎蒙多氏病是一种罕见且未被认识的良性生殖器疾病,由阴茎背浅静脉的孤立血栓组成。症状不明显,也有无症状的病例。患者通常表现为阴茎背部的索状硬结。诊断通常基于病史和体格检查。影像学在蒙多氏病中的作用是识别血管内血栓。在诊断不确定的情况下,灰度和多普勒超声可用于检测血栓形成的程度,显示静脉腔内的回声物质,血管不可压缩性和无血流,以及痛苦的选择性压力。磁共振成像的使用是有争议的,并没有常规使用。通常治疗是保守的:性休息,局部麻醉剂,消炎药,感染时使用抗生素和抗凝血剂。硬化性淋巴管炎和佩罗尼氏病已被描述为可能的鉴别诊断。
{"title":"Penile Mondor's disease: Imaging in two cases.","authors":"Michele Foresti,&nbsp;Andrea Parmiggiani","doi":"10.3941/jrcr.v14i12.3926","DOIUrl":"https://doi.org/10.3941/jrcr.v14i12.3926","url":null,"abstract":"<p><p>Penile Mondor's disease is a rare and under-recognized benign genital condition consisting of an isolated thrombosis of the dorsal superficial vein of the penis. Symptoms do not show distinctive features and there are asymptomatic cases. The patients usually present with a cord-like induration at dorsum of the penis. Diagnosis is usually made based on history and physical examination. The role of imaging in Mondor's disease is to identify the intravascular thrombus. In case of diagnostic uncertainty, Grey scale and Doppler ultrasound can be useful to detect the extent of thrombosis demonstrating echogenic material within venous lumen, vessel incompressibility and absence of flow, as well as painful selective pressure. The use of Magnetic Resonance imaging is controversial and not used routinely. Usually treatment is conservative: sexual rest, local anesthetics, anti-inflammatories, antibiotics in case of infection and anticoagulants. Sclerosing lymphangitis and Peyronie's disease have been described as possible differential diagnosis.</p>","PeriodicalId":46520,"journal":{"name":"Journal of Radiology Case Reports","volume":"14 12","pages":"24-30"},"PeriodicalIF":1.0,"publicationDate":"2020-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943046/pdf/jrcr-14-12-24.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25476888","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: 2
Malignant transformation in a sciatic plexiform neurofibroma in Neurofibromatosis Type 1 - imaging features that aid diagnosis. 1型神经纤维瘤病中坐骨丛状神经纤维瘤的恶性转化:辅助诊断的影像学特征。
IF 1 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2020-12-31 eCollection Date: 2020-12-01 DOI: 10.3941/jrcr.v14i12.4028
Dorinda Chee Yee Chew, Daniel Bin Hang Zhao, Kesavan Sittampalam, S Krishna Kumar

A 41-year-old Asian male with NF1 and bilateral sciatic plexiform neurofibromas, presented with unintentional weight loss, increasing size of a left thigh mass associated with increasing pain and radiculopathy. MRI of the left thigh demonstrated imaging features suspicious of malignant transformation. The patient had a new left lung mass, demonstrating avid FDG uptake, raising suspicion for metastasis. Surgical resection of the left thigh mass confirms malignant transformation in a preexisting sciatic plexiform neurofibroma. Diagnosis of malignant transformation in a nerve sheath tumour can be challenging. MRI remains the main preferred imaging modality in the evaluation of these tumours. Imaging features that raise suspicion for malignant transformation are discussed. Although none of these are specific for malignant transformation, studies suggest that the presence of two to four of these features should prompt further investigations.

41岁亚洲男性,患有NF1和双侧坐骨丛状神经纤维瘤,表现为体重意外减轻,左大腿肿块增大,伴有疼痛和神经根病。左大腿MRI显示疑似恶性转化的影像学特征。患者有一个新的左肺肿块,显示FDG摄取旺盛,引起转移的怀疑。手术切除左大腿肿块证实了先前存在的坐骨丛状神经纤维瘤的恶性转化。神经鞘肿瘤恶性转化的诊断具有挑战性。MRI仍然是评估这些肿瘤的主要首选成像方式。讨论了引起恶性转化怀疑的影像学特征。虽然这些都不是恶性转化所特有的,但研究表明,其中两到四种特征的存在应该促使进一步的研究。
{"title":"Malignant transformation in a sciatic plexiform neurofibroma in Neurofibromatosis Type 1 - imaging features that aid diagnosis.","authors":"Dorinda Chee Yee Chew,&nbsp;Daniel Bin Hang Zhao,&nbsp;Kesavan Sittampalam,&nbsp;S Krishna Kumar","doi":"10.3941/jrcr.v14i12.4028","DOIUrl":"https://doi.org/10.3941/jrcr.v14i12.4028","url":null,"abstract":"<p><p>A 41-year-old Asian male with NF1 and bilateral sciatic plexiform neurofibromas, presented with unintentional weight loss, increasing size of a left thigh mass associated with increasing pain and radiculopathy. MRI of the left thigh demonstrated imaging features suspicious of malignant transformation. The patient had a new left lung mass, demonstrating avid FDG uptake, raising suspicion for metastasis. Surgical resection of the left thigh mass confirms malignant transformation in a preexisting sciatic plexiform neurofibroma. Diagnosis of malignant transformation in a nerve sheath tumour can be challenging. MRI remains the main preferred imaging modality in the evaluation of these tumours. Imaging features that raise suspicion for malignant transformation are discussed. Although none of these are specific for malignant transformation, studies suggest that the presence of two to four of these features should prompt further investigations.</p>","PeriodicalId":46520,"journal":{"name":"Journal of Radiology Case Reports","volume":"14 12","pages":"1-13"},"PeriodicalIF":1.0,"publicationDate":"2020-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943044/pdf/jrcr-14-12-1.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25476886","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
Involvement of the Mediastinal Subpleural Pulmonary Parenchyma on Chest CT in COVID-19 patients: A Case Series. COVID-19 患者胸部 CT 显示纵隔胸膜下肺实质受累:病例系列。
IF 1 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2020-11-30 eCollection Date: 2020-11-01 DOI: 10.3941/jrcr.v14i11.3974
Luigi Urciuoli, Elvira Guerriero, Lanfranco Musto

Coronavirus disease 2019 (COVID-19) is an infectious disease caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). First identified in December 2019 in Wuhan, China, it has since become a global pandemic. Although the reference standard for SARS-CoV-2 diagnosis is real-time reverse transcription polymerase chain reaction (RT-PCR), computed tomography (CT) is recommended for both initial evaluation and follow-up. The CT findings in COVID-19 are varied, but typical ground-glass opacities are usually reported to occupy a peripheral costal subpleural distribution. Here we report eight confirmed COVID-19 cases who underwent clinical evaluation, laboratory testing, and unenhanced chest CT. In all patients, chest CT showed the presence of ground-glass opacities in the mediastinal subpleural parenchyma. While these cases also showed the typical CT features of COVID-19, involvement of the mediastinal subpleural parenchyma should not lower the index of suspicion for COVID-19.

冠状病毒病 2019(COVID-19)是由严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)引起的一种传染病。它于 2019 年 12 月在中国武汉首次发现,此后成为一种全球性流行病。虽然 SARS-CoV-2 诊断的参考标准是实时反转录聚合酶链反应(RT-PCR),但建议在初步评估和随访时使用计算机断层扫描(CT)。COVID-19的CT结果多种多样,但据报道,典型的磨玻璃不透明通常呈肋膜下周围分布。在此,我们报告了 8 例确诊的 COVID-19 患者,他们接受了临床评估、实验室检查和非增强胸部 CT。所有患者的胸部 CT 均显示纵隔胸膜下实质存在磨玻璃不透明。虽然这些病例也显示出 COVID-19 的典型 CT 特征,但纵隔胸膜下实质受累不应降低对 COVID-19 的怀疑指数。
{"title":"Involvement of the Mediastinal Subpleural Pulmonary Parenchyma on Chest CT in COVID-19 patients: A Case Series.","authors":"Luigi Urciuoli, Elvira Guerriero, Lanfranco Musto","doi":"10.3941/jrcr.v14i11.3974","DOIUrl":"10.3941/jrcr.v14i11.3974","url":null,"abstract":"<p><p>Coronavirus disease 2019 (COVID-19) is an infectious disease caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). First identified in December 2019 in Wuhan, China, it has since become a global pandemic. Although the reference standard for SARS-CoV-2 diagnosis is real-time reverse transcription polymerase chain reaction (RT-PCR), computed tomography (CT) is recommended for both initial evaluation and follow-up. The CT findings in COVID-19 are varied, but typical ground-glass opacities are usually reported to occupy a peripheral costal subpleural distribution. Here we report eight confirmed COVID-19 cases who underwent clinical evaluation, laboratory testing, and unenhanced chest CT. In all patients, chest CT showed the presence of ground-glass opacities in the mediastinal subpleural parenchyma. While these cases also showed the typical CT features of COVID-19, involvement of the mediastinal subpleural parenchyma should not lower the index of suspicion for COVID-19.</p>","PeriodicalId":46520,"journal":{"name":"Journal of Radiology Case Reports","volume":"14 11","pages":"1-15"},"PeriodicalIF":1.0,"publicationDate":"2020-11-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7942959/pdf/jrcr-14-11-1.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25479774","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
期刊
Journal of Radiology Case Reports
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:604180095
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