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Case Reports in Radiology最新文献

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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。
Case Reports in Radiology 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
{"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":null,"pages":null},"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
Upper Limb Meromelia with Oligodactyly and Brachymesophalangy of the Foot: An Unusual Association 上肢缺趾畸形伴足少趾和足短管畸形:一种不寻常的关联
Case Reports in Radiology Pub Date : 2019-06-24 DOI: 10.1155/2019/3419383
M. Özdemir, R. Kavak, Ö. Eraslan
{"title":"Upper Limb Meromelia with Oligodactyly and Brachymesophalangy of the Foot: An Unusual Association","authors":"M. Özdemir, R. Kavak, Ö. Eraslan","doi":"10.1155/2019/3419383","DOIUrl":"https://doi.org/10.1155/2019/3419383","url":null,"abstract":"Meromelia is a rare skeletal abnormality characterized by the partial absence of at least one limb. Several mechanisms have been postulated to explain the etiopathogenesis of the disorder. Most of the cases of meromelia are reported to be sporadic. It can occur either in isolation or with other congenital malformations. VACTERL association, gastroschisis, atrial septal defect, proximal femoral focal deficiency, and fibular hemimelia are the congenital abnormalities reported to be in association with meromelia. However, no other congenital abnormalities in association with meromelia have been recorded to date. We herein present an unusual case of bilateral upper limb meromelia accompanied by unilateral oligodactyly and brachymesophalangy of the foot.","PeriodicalId":30326,"journal":{"name":"Case Reports in Radiology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2019-06-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77233803","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: 2
Microgallbladder: Self-Remitting Acute Cholecystitis-Like Condition Unique to Patients with Cystic Fibrosis 微胆囊:囊性纤维化患者特有的自缓解急性胆囊炎样疾病
Case Reports in Radiology Pub Date : 2019-06-19 DOI: 10.1155/2019/6737428
Mina S Mousa, J. Feldman, Paresh Mahajan
{"title":"Microgallbladder: Self-Remitting Acute Cholecystitis-Like Condition Unique to Patients with Cystic Fibrosis","authors":"Mina S Mousa, J. Feldman, Paresh Mahajan","doi":"10.1155/2019/6737428","DOIUrl":"https://doi.org/10.1155/2019/6737428","url":null,"abstract":"Microgallbladder is a nonsurgical medical condition characterized by chronic inflammation and atrophy of the gallbladder, which is considered a highly specific imaging finding unique to patients with cystic fibrosis (CF), and has been incidentally reported on abdominal imaging in up to 45% of cases with CF. The impairment of exocrine water efflux in CF leads to the production of hyperviscous biliary secretions, cholestasis, and transient cystic duct obstruction of the microgallbladder causing microcholecystitis—interestingly a self-remitting acute cholecystitis-like condition without surgical intervention. We present a case report of a 22-year-old male patient with history of CF with multiple hospital admissions for unexplained chronic abdominal pain found to be caused by microgallbladder, which was managed conservatively.","PeriodicalId":30326,"journal":{"name":"Case Reports in Radiology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2019-06-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85371757","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
Two Cases of Primary Testicular Lymphoma Presenting with Direct Spread along the Spermatic Cord and Gonadal Vessels 原发性睾丸淋巴瘤沿精索及性腺血管直接扩散2例
Case Reports in Radiology Pub Date : 2019-06-18 DOI: 10.1155/2019/5953618
M. Ellatif, Raekha Kumar, A. Weller, D. Katz, E. Vrentzou
{"title":"Two Cases of Primary Testicular Lymphoma Presenting with Direct Spread along the Spermatic Cord and Gonadal Vessels","authors":"M. Ellatif, Raekha Kumar, A. Weller, D. Katz, E. Vrentzou","doi":"10.1155/2019/5953618","DOIUrl":"https://doi.org/10.1155/2019/5953618","url":null,"abstract":"Primary testicular lymphoma is a rare testicular neoplasm that mainly affects elderly patients, with Human Immunodeficiency Virus (HIV) being a known risk factor in the younger population. Approximately 20% of patients will have disseminated disease with extra-nodal involvement at clinical presentation. Rarely, direct spread along the spermatic cord and gonadal vessels can occur and has been described in the literature. We present two cases of this phenomenon where the primary testicular tumour has spread along the gonadal vein to its origin at the inferior vena cava.","PeriodicalId":30326,"journal":{"name":"Case Reports in Radiology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2019-06-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90298854","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: 7
Cholecystohepatic Duct: A Biliary Duct Variant Resulting in Postcholecystectomy Bile Leak—Case Report and Review of Normal and Common Variant Biliary Anatomy 胆囊-肝管:胆囊切除术后胆漏的一种胆管变异——正常和常见变异胆道解剖的病例报告和回顾
Case Reports in Radiology Pub Date : 2019-06-17 DOI: 10.1155/2019/6812793
Nathan Meyer, S. Al-katib, Farnoosh Sokhandon
{"title":"Cholecystohepatic Duct: A Biliary Duct Variant Resulting in Postcholecystectomy Bile Leak—Case Report and Review of Normal and Common Variant Biliary Anatomy","authors":"Nathan Meyer, S. Al-katib, Farnoosh Sokhandon","doi":"10.1155/2019/6812793","DOIUrl":"https://doi.org/10.1155/2019/6812793","url":null,"abstract":"Although relatively infrequent, bile duct leaks are among the primary complications of hepatobiliary surgery and cholecystectomy given the large number of these operations performed annually around the world. Variant biliary anatomy increases the risk of surgical complications, especially if unrecognized on preoperative imaging or intraoperatively. Presented here is a case of a patient with an unrecognized cholecystohepatic duct at the time of surgery leading to bile leak after cholecystectomy. Numerous factors made for a technically difficult surgery with obscuration of the true anatomy, ultimately resulting in transection of the cholecystohepatic duct. Understanding normal and variant biliary anatomy will help prevent avoidable complications of hepatobiliary surgery.","PeriodicalId":30326,"journal":{"name":"Case Reports in Radiology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2019-06-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80297218","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
Dural and Leptomeningeal Spine Metastases of Breast Cancer. 乳腺癌的硬脊膜和脊膜脊柱转移。
Case Reports in Radiology Pub Date : 2019-05-29 eCollection Date: 2019-01-01 DOI: 10.1155/2019/4289362
Fernando Matos, Luís Cerqueira
{"title":"Dural and Leptomeningeal Spine Metastases of Breast Cancer.","authors":"Fernando Matos,&nbsp;Luís Cerqueira","doi":"10.1155/2019/4289362","DOIUrl":"https://doi.org/10.1155/2019/4289362","url":null,"abstract":"<p><p>We present a case of a 57-year-old female diagnosed with invasive ductal breast cancer, which was treated and in remission for 12 years. In 2018 she presented a progressive dorsal back pain, which prevented her from performing basic tasks. An MR study was performed and revealed the presence of an extramedullary metastatic sleeve located in the thoracic intradural space. Concomitant multiple small nodular foci were adhering diffusely to the spinal cord, compatible with leptomeningeal metastatic disease. The occurrence of both forms of spread in the spine is uncommon, and its distinction on imaging is of particular importance taking into account the differences in treatment approach and prognosis.</p>","PeriodicalId":30326,"journal":{"name":"Case Reports in Radiology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2019-05-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2019/4289362","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37119921","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
Case Report of a Rare Cystic Mediastinal Lymphangioma Mimicking Recurrent Pleural Effusion. 罕见的囊性纵隔淋巴管瘤表现为复发性胸腔积液1例报告。
Case Reports in Radiology Pub Date : 2019-05-26 eCollection Date: 2019-01-01 DOI: 10.1155/2019/1301845
Fateme Salehi, Mark Landis, Richard Inculet, Daniele Wiseman
{"title":"Case Report of a Rare Cystic Mediastinal Lymphangioma Mimicking Recurrent Pleural Effusion.","authors":"Fateme Salehi,&nbsp;Mark Landis,&nbsp;Richard Inculet,&nbsp;Daniele Wiseman","doi":"10.1155/2019/1301845","DOIUrl":"https://doi.org/10.1155/2019/1301845","url":null,"abstract":"<p><p>Mediastinal lymphangiomas are rare benign congenital malformations, but complications can occur, including infection, cystic hemorrhage, superior vena cava syndrome, airway compromise, and chylothorax. Radiologically, lymphangiomas are well-defined masses, with low attenuation ranging from simple to complex fluid and fat. They often encase adjacent mediastinal structures. We present a case of mediastinal lymphangioma in a young female, who presented with recurrent complex pleural effusions, initially thought to represent an empyema and/or necrotic mass. Despite surgical chest tube and interventional radiology drainage, fluid reaccumulated. Upon further review, the interventional and thoracic radiologist concurred that the complex collection was in fact predominantly extra pleural in location. The patient underwent partial resection after it was discovered intraoperatively that the extra pleural cystic mass was contiguous with and extended deeply into the mediastinum. Histopathology confirmed the diagnosis of lymphangioma.</p>","PeriodicalId":30326,"journal":{"name":"Case Reports in Radiology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2019-05-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2019/1301845","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37367651","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
An Unusual Ovarian Mucinous Borderline Tumor with a Large Solid Component. 罕见的卵巢黏液交界性肿瘤伴大实性成分。
Case Reports in Radiology Pub Date : 2019-05-22 eCollection Date: 2019-01-01 DOI: 10.1155/2019/1402736
Eito Kozawa, Kaiji Inoue, Mitsutake Yano, Masanori Yasuda, Kosei Hasegawa, Junji Tanaka, Tomoaki Ichikawa, Mamoru Niitsu
{"title":"An Unusual Ovarian Mucinous Borderline Tumor with a Large Solid Component.","authors":"Eito Kozawa,&nbsp;Kaiji Inoue,&nbsp;Mitsutake Yano,&nbsp;Masanori Yasuda,&nbsp;Kosei Hasegawa,&nbsp;Junji Tanaka,&nbsp;Tomoaki Ichikawa,&nbsp;Mamoru Niitsu","doi":"10.1155/2019/1402736","DOIUrl":"https://doi.org/10.1155/2019/1402736","url":null,"abstract":"<p><p>Herein, we report magnetic resonance imaging (MRI) findings of a mucinous borderline tumor of the ovary, which we observed as a mainly solid tumor with large solid components in the lower pelvic cavity. The appearance of ovarian epithelial tumors on imaging is often complex. Cystic to solid appearing masses may be observed, and they often resemble epithelial carcinoma. Due to mucinous or hemorrhage components of packed small or microcystic components, MRI depicts slightly high signal intensity on T1-weighted images and low signal intensity on T2-weighted images. Mucinous borderline tumor of the ovary with a large solid component is very rare, but it is clinically important to recognize the possibility of mucinous borderline tumor to avoid unnecessary surgical intervention.</p>","PeriodicalId":30326,"journal":{"name":"Case Reports in Radiology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2019-05-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2019/1402736","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37367652","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: 3
TB Meningitis and TB Peritonitis: Abdominal Pseudocyst and VP-Shunt Link. 结核性脑膜炎和结核性腹膜炎:腹部假性囊肿和vp -分流链。
Case Reports in Radiology Pub Date : 2019-04-28 eCollection Date: 2019-01-01 DOI: 10.1155/2019/4893547
Manzoor Ahmed, Essameldin Ali ElGamal, Anwar Ahmad, Muhammad Badar Zaman
{"title":"TB Meningitis and TB Peritonitis: Abdominal Pseudocyst and VP-Shunt Link.","authors":"Manzoor Ahmed,&nbsp;Essameldin Ali ElGamal,&nbsp;Anwar Ahmad,&nbsp;Muhammad Badar Zaman","doi":"10.1155/2019/4893547","DOIUrl":"https://doi.org/10.1155/2019/4893547","url":null,"abstract":"<p><p>TB meningitis (TBM) carries high morbidity and mortality and is a relatively common extrapulmonary TB in the third world countries. TBM as thick exudative disease manifests on MRI and CT as nodular basal leptomeningitis, hydrocephalus, basal infarcts, and tuberculomas. Hydrocephalus is treated with ventriculoperitoneal shunting (VPS). Shunt malfunction and revision are common. We report a case of multidrug-resistant TBM with spinal involvement and dissemination of the disease via VPS causing TB peritonitis (TBP). TBP presented as a large abdominal pseudocyst around the catheter tip with shunt malfunction. There was no evidence for any other site of extra-CNS disease. TBP per se is relatively less common. This is the first case reporting VPS as a means of TB spread.</p>","PeriodicalId":30326,"journal":{"name":"Case Reports in Radiology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2019-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2019/4893547","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37315156","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
Transcatheter Proximal Coil Blocking with n-Butyl-2-Cyanoacrylate Injection via the Pulmonary Artery Alone for Rasmussen's Aneurysm. 经肺动脉注射正丁基-2-氰基丙烯酸酯近端线圈阻断治疗拉斯穆森动脉瘤。
Case Reports in Radiology Pub Date : 2019-04-15 eCollection Date: 2019-01-01 DOI: 10.1155/2019/1725238
Atsushi Ugajin, Hiroyuki Fujii, Hiroyasu Nakamura, Akifumi Fujita, Takahiro Sasaki, Naoko Mato, Hideharu Sugimoto
{"title":"Transcatheter Proximal Coil Blocking with n-Butyl-2-Cyanoacrylate Injection via the Pulmonary Artery Alone for Rasmussen's Aneurysm.","authors":"Atsushi Ugajin,&nbsp;Hiroyuki Fujii,&nbsp;Hiroyasu Nakamura,&nbsp;Akifumi Fujita,&nbsp;Takahiro Sasaki,&nbsp;Naoko Mato,&nbsp;Hideharu Sugimoto","doi":"10.1155/2019/1725238","DOIUrl":"https://doi.org/10.1155/2019/1725238","url":null,"abstract":"<p><p>Rasmussen's aneurysm is a peripheral pulmonary artery pseudoaneurysm (PAP) within a tuberculosis cavity. Because it can be perfused from the bronchial and pulmonary arterial circulations, combined embolization via the bronchial and pulmonary arteries is sometimes required. Herein, we present case of a 51-year-old man with Rasmussen's aneurysm that was successfully treated by proximal coil blocking with n-butyl-2-cyanoacrylate (NBCA) injection via the pulmonary artery alone. With proximal coil blocking, a sufficient amount of NBCA could be injected without unintended reflux of the NBCA cast to the proximal pulmonary artery. To our knowledge, there has been no report that attempted NBCA injection under proximal coil blocking for Rasmussen's aneurysm. Our treatment approach may be safe and effective for infectious lung disease-related PAP, which has to be treated from the pulmonary artery side.</p>","PeriodicalId":30326,"journal":{"name":"Case Reports in Radiology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2019-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2019/1725238","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37282388","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
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