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Ventriculocoronary Fistulas with Hypoplastic Left Heart in a Neonate: Imaging with Cardiac CT. 新生儿左心发育不全的心室冠状动脉瘘:心脏CT成像。
Pub Date : 2021-03-16 eCollection Date: 2021-01-01 DOI: 10.1155/2021/6657447
Serap Baş, Utku Alkara

Fistulous communications between the ventricular cavities and the coronary arterial tree can be found in the presence of hypoplasia of the left ventricle, especially when the ventricular septum is intact and mitral stenosis and aortic atresia subtype are present. The cardiac CT provides excellent anatomic information especially in the evaluation of extracardiac vessels and coronary arteries. In this case study, we report a newborn with ventriculocoronary fistulas (VCFs) with the hypoplastic left disease diagnosed with cardiac CT. Transthoracic echocardiography of a term baby showed hypoplastic left heart syndrome (HLHS) with mitral stenosis and aortic atresia. The patient immediately underwent a Sano variation of the Norwood procedure. On the postoperative second day, the clinical status of the patient deteriorated. A prospective electrocardiogram-gated axial technique was performed within a single heartbeat for the patient and large VCFs were detected and a second operation were performed to close the VCFs that failed. On the nineteenth day after the operation, the baby passed away. According to us, cardiac CT can also be performed free-breathing and without anesthesia in the neonatal period for the definition of complex cardiac anatomy with the lower radiation dose from the latest scanners, radiation risk of CT should be weighed against the anesthesia risk of cardiac MRI and intraoperative risk of conventional cardiac angiography. Pre-operative cardiac CT may increase surgical success.

在左心室发育不全的情况下,特别是当室间隔完整、二尖瓣狭窄和主动脉闭锁亚型存在时,可以发现心室腔和冠状动脉树之间的瘘状交通。心脏CT提供了很好的解剖信息,特别是在评估心外血管和冠状动脉。在这个病例研究中,我们报告了一个新生儿心室冠状动脉瘘(VCFs)与心脏CT诊断的左发育不全疾病。经胸超声心动图显示左心发育不良综合征(HLHS)伴有二尖瓣狭窄和主动脉闭锁。患者立即接受了诺伍德手术的Sano变异。术后第2天,患者临床状况恶化。在患者单次心跳中进行前瞻性心电图门控轴向技术,检测到较大的vcf,并进行第二次手术以关闭失败的vcf。手术后的第十九天,婴儿去世了。我们认为,新生儿期心脏CT也可以自由呼吸、不麻醉进行,由于心脏解剖结构复杂,最新扫描仪的辐射剂量较低,CT的辐射风险应与心脏MRI的麻醉风险和常规心脏血管造影的术中风险进行权衡。术前心脏CT可提高手术成功率。
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引用次数: 0
Refractory Biliary Catheter Leak Corrected by a Hybrid Closed Loop Catheter-Pump System. 复合式闭环导管-泵系统纠正顽固性胆管泄漏。
Pub Date : 2021-03-09 eCollection Date: 2021-01-01 DOI: 10.1155/2021/6677500
Ravi Murthy, Varun Rachakonda, Juri Bassuner

The development of inoperable biliary obstruction in patients with liver, biliary, and pancreatic neoplasia is commonplace particularly in the advanced stages of these diseases. Under these circumstances, restoring bile flow to the gut is paramount in reestablishing homeostasis. Hitherto, this has been achieved by utilizing passive, gravity-dependent bilioenteric conduits with the use of perforated plastic catheters or metallic stents inserted either in a percutaneous transhepatic fashion or via endoscopic techniques. A frequent untoward event of biliary decompression utilizing percutaneous transhepatic catheters (PTC) is the development of pain, cholangitis, hyperbilirubinemia, or pericatheter bile leak due to the suboptimal normalization of bile flow. In some instances, the etiology of PTC malfunction can be correctly ascribed to catheter malposition and/or catheter lumen obstruction; however, in the majority, it remains radiographically occult on transcatheter cholangiography-the "gold standard." Regardless of findings, the management remains fluoroscopic repositioning or exchanges for larger diameter catheters to attempt to seal the pericatheter potential space and prevent bile seepage. Unfortunately, these maneuvers are met with limited and unpredictable levels of success. We present the successful management of an instance of recalcitrant external pericatheter bile leak mitigated by employing a hybrid closed loop biliary catheter-pump system by employing an assortment of FDA approved off-the-shelf medical devices.

不能手术的胆道梗阻在肝脏、胆道和胰腺肿瘤患者中是常见的,特别是在这些疾病的晚期。在这种情况下,恢复胆汁流向肠道是重建体内平衡的首要任务。到目前为止,这是通过使用被动的、重力依赖的胆道导管来实现的,使用穿孔塑料导管或金属支架,通过经皮经肝方式或通过内窥镜技术插入。使用经皮经肝导管(PTC)进行胆道减压时,常见的不良事件是由于胆流量未达到最佳正常化而导致疼痛、胆管炎、高胆红素血症或导管周围胆漏。在某些情况下,PTC功能障碍的病因可以正确地归因于导管错位和/或导管管腔阻塞;然而,在大多数情况下,它在经导管胆道造影(“金标准”)中仍然是隐匿的。无论结果如何,处理方法仍然是在透视下重新定位或更换更大直径的导管,以试图密封导管周围的潜在空间,防止胆汁渗漏。不幸的是,这些演习的成功程度有限且不可预测。我们提出了一个成功的管理难治性外导管胆漏的实例,通过采用混合闭环胆管泵系统,通过采用各种FDA批准的现成的医疗设备减轻。
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引用次数: 0
Fetus in Fetu in an Adult Female and Brief Review of Literature. 一名成年女性的胎儿和文献简评。
Pub Date : 2021-02-11 eCollection Date: 2021-01-01 DOI: 10.1155/2021/6660277
Saroj Sharma, Prashant Kumar Gupta, Basanta Regmi, Aarti Gupta, Upasana Lamichhane

Fetus in fetu (FIF) is a very rare condition in which malformed fetus is found within the body of a living twin, most commonly within the retroperitoneum. It is a parasitic fetal twin of a diamniotic, monozygotic type. It should be differentiated from teratoma by the presence of organized vertebral column and appropriately arranged other organs or limbs around it. There is no such axial arrangement in teratoma, which has also got definite malignant potential. We report a case of FIF in a 21-year-old lady who presented late with nonspecific abdominal symptoms. Preoperative diagnosis of FIF in this case was made on computed tomography, and the patient underwent exploratory laparotomy with complete excision of mass. The excised mass in a sac was proven to be FIF on the basis of gross and histopathological examination. Surgical excision is the ideal treatment even teratoma being the differential diagnosis.

胎儿畸形(Fetus in fetu,FIF)是一种非常罕见的情况,畸形胎儿存在于活体双胞胎体内,最常见的是在腹膜后。它是一种单卵双胎型的寄生胎儿。它与畸胎瘤的区别在于畸胎瘤周围存在有组织的椎体和适当排列的其他器官或肢体。畸胎瘤没有这种轴向排列,也具有明确的恶性潜能。我们报告了一例 21 岁女性的 FIF,她因非特异性腹部症状就诊较晚。该病例术前通过计算机断层扫描确诊为 FIF,患者接受了探查性开腹手术并完全切除了肿块。根据大体和组织病理学检查,切除的囊性肿块被证实为 FIF。即使畸胎瘤是鉴别诊断,手术切除也是理想的治疗方法。
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引用次数: 0
Parastomal Gallbladder Herniation as an Incidental Preoperative Computed Tomography Finding. 造口旁胆囊疝作为一种偶然的术前计算机断层扫描发现。
Pub Date : 2021-02-11 eCollection Date: 2021-01-01 DOI: 10.1155/2021/8864347
Magdalini Smarda, Konstantinos Manes, Dimitrios Fagkrezos, Dimitrios Argiropoulos, Konstantinos Laios, Charickleia Triantopoulou, Petros Maniatis

A 65-year-old woman with a long surgical history was referred to our hospital's Colorectal Unit for ileostomy management. The patient retained an ileostomy for almost a decade after a series of complicated operations she had undergone, which had several side effects such as electrolyte imbalances, high output, weight loss, and a parastomal hernia. Our hospital's colorectal surgeon proposed to replace the ileostomy with a permanent sigmoidostomy and asked for an imaging evaluation of the parastomal hernia content before the surgery. A computed tomography of the abdomen was performed using our Computed Tomography Department's 64-detector row CT scanner after oral administration of contrast media, without intravenous contrast media injection due to allergy. Concerning the parastomal ileostomal hernia, besides small bowel loops with intraluminal gastrografin, inside the parastomal hernial sac, there also was an almost rounded cystic lesion. Absence of the gallbladder at its typical position and no record of cholecystectomy raised suspicion for gallbladder projection inside the sac. Our suspicion was confirmed during the surgery. Nonexisting acute cholecystitis allowed easy reduction of the gallbladder along with the small bowel loops inside the peritoneal cavity, without proceeding to cholecystectomy at the same time. Finally, ileostomy was annulated and an end colostomy was established. Four days after the surgery, the patient was discharged from the hospital and was happy to live an almost normal life thereafter.

一位65岁的女性,有长期的手术史,被转介到我院结直肠科进行回肠造口治疗。在经历了一系列复杂的手术后,患者保留了近十年的回肠造口术,这些手术有一些副作用,如电解质失衡、高排尿量、体重减轻和造口旁疝。本院结直肠外科医生建议将回肠造口术改为乙状结肠永久性造口术,并要求术前对造口旁疝内容物进行影像学评估。经口服造影剂,未因过敏静脉注射造影剂,使用我院计算机断层科64排CT扫描腹部。造口旁回造口疝,除腔内有胃grafin的小肠袢外,造口旁疝囊内也有近圆形的囊性病变。胆囊在其典型位置缺失且无胆囊切除术记录,引起胆囊囊内突出的怀疑。我们的怀疑在手术中得到了证实。不存在的急性胆囊炎使得胆囊和腹膜腔内的小肠袢容易缩小,而不需要同时进行胆囊切除术。最后将回肠造口术进行环结,并建立末端结肠造口术。手术四天后,病人出院了,从此过着几乎正常的生活。
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引用次数: 4
Giant Basal Cell Carcinoma of the Scalp with Intracranial Invasion: MRI Findings with Tract Visualisation. 侵袭颅内的头皮巨大基底细胞癌:具有束状影像的MRI表现。
Pub Date : 2021-02-10 eCollection Date: 2021-01-01 DOI: 10.1155/2021/6675199
Maria Brunella Cipullo, Elham Rahimian, Majid Tahsini, Zoi Giavri, Sotirios Bisdas

A rare case of recurrent basal cell carcinoma in the scalp that infiltrated multiple intracranial structures is presented. Basal cell carcinoma represents one of the most frequent malignant nonmelanotic skin neoplasms, but the majority of them have no aggressive and recurrent behaviour. The aim of this case report is to provide an overview of the main clinical and radiologic features of basal cell carcinoma, focusing on the conventional and advanced (tractography) MRI findings and providing an overview of treatment and prognosis.

本文报告一例罕见的复发性头皮基底细胞癌,其浸润于多个颅内结构。基底细胞癌是最常见的恶性非黑色素皮肤肿瘤之一,但大多数没有侵袭性和复发性行为。本病例报告的目的是概述基底细胞癌的主要临床和放射学特征,重点是常规和晚期(导管造影)MRI表现,并概述治疗和预后。
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引用次数: 1
Intermetatarsal Coalition: Case Report, Literature Review, and Imaging Findings of an Underrecognized and Underdiagnosed Cause of Foot Pain. 跖骨间联合:病例报告,文献回顾,以及未被充分认识和诊断的足痛原因的影像学表现。
Pub Date : 2021-02-08 eCollection Date: 2021-01-01 DOI: 10.1155/2021/6667907
WanYin Lim, Steven Zadow, Angela Moran, Jonathan Heysen

Coalition is defined as abnormal bridging between two bones, and the connection can be osseous or nonosseous. Most coalitions in the foot involve the hindfoot. Intermetatarsal coalition is thought to be much rarer than the more common hindfoot coalitions and has only been reported sporadically in the orthopedic literature. We present two patients with nonosseous intermetatarsal coalition presenting with nonspecific dorsolateral foot pain and describe the imaging findings of intermetatarsal coalition with different modalities. We suspect that whilst rarely described, intermetatarsal coalition is quite likely a more common underrecognized entity than a rare entity. This report is aimed at increasing the awareness of coalition in this location, in the radiology community, particularly the nonosseous ones, given that this condition can be debilitating but treatable.

连接被定义为两根骨头之间的异常桥接,连接可以是骨性的或非骨性的。大多数足部的结扎都发生在后脚。跖骨间联合被认为比更常见的后足联合要罕见得多,在骨科文献中仅偶有报道。我们报告了两例以非特异性足背外侧疼痛为表现的非骨性跖骨间联盟患者,并描述了不同形式的跖骨间联盟的影像学表现。我们怀疑,虽然很少被描述,但跖骨间关节联合很可能是一种更常见的未被充分认识的实体,而不是罕见的实体。本报告旨在提高放射界对该部位联合的认识,特别是非骨性联合,因为这种情况可能使人衰弱,但可以治疗。
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引用次数: 0
Epilepsy as a Presentation of a Neuroglial Cyst Associated with Dysgenesis of Corpus Callosum in a Child. 癫痫是儿童胼胝体发育不良相关的神经胶质囊肿的表现。
Pub Date : 2021-01-21 eCollection Date: 2021-01-01 DOI: 10.1155/2021/6675071
Outznit Mustapha, Nazik Allali, Chat Latifa, Siham El Haddad

Neuroglial (glioependymal) cyst is a rare congenital tumor of the central nervous system usually found in childhood. It can be isolated or associated with other brain malformations. Magnetic resonance imaging is the technique of choice for making the diagnosis. We report the case of a 10-year-old child who presented with epileptic seizures revealing a neuroglial cyst and dysgenesis of the corpus callosum.

摘要神经胶质(胶质室管膜)囊肿是一种罕见的先天性中枢神经系统肿瘤,常见于儿童。它可以是孤立的,也可以与其他脑畸形相关联。磁共振成像是诊断的首选技术。我们报告的情况下,一个10岁的孩子谁提出了癫痫发作显示神经胶质囊肿和胼胝体发育不良。
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引用次数: 1
Amyotrophic Monoplegia Secondary to Posttraumatic Rupture of the Brachial Plexus's Roots: A Case Report and Review of the Literature. 创伤后臂丛神经根断裂继发肌萎缩性单瘫1例报告及文献复习。
Pub Date : 2021-01-01 DOI: 10.1155/2021/6614881
Oumniya Abouhanine, Hasnaa Belgadir, Vianney Ndayishimiye, Omar Amriss, Aicha Merzem, Nadia Moussali, Naima El Benna

Brachial plexus lesions most often occur in multiple trauma. We report a case of a 37-year-old patient who presented an upper left limb total sensitivomotor deficit and amyotrophy after a cervical and upper limb trauma. Cervical magnetic resonance imaging (MRI) was performed. It noted pseudomeningoceles at the levels of C6-C7, C7-D1, and D1-D2 in T1 hyposignal , T2 and STIR hypersignal , not enhanced by the injection of Gadolinium extending in foraminal and extraforaminal spaces without visualization of the corresponding rootlets. Traumatic brachial plexus injury is a potentially serious debilitating injury which can be well explored on MRI.

臂丛病变多发生于多发创伤。我们报告一例37岁的患者,在颈椎和上肢外伤后出现左上肢完全敏感运动障碍和肌萎缩。行宫颈磁共振成像(MRI)检查。在T1低信号、T2和STIR高信号区,可见C6-C7、C7-D1和D1-D2水平的假性脑膜膨出,注射钆不增强,向椎间孔和椎间孔外间隙延伸,未见相应的根状突起。外伤性臂丛神经损伤是一种潜在的严重的衰弱性损伤,MRI可以很好地探讨这种损伤。
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引用次数: 0
Coil Embolization of Arc of Buhler Aneurysm Rupture. 螺旋栓塞治疗布勒动脉瘤破裂弧线。
Pub Date : 2020-12-11 eCollection Date: 2020-01-01 DOI: 10.1155/2020/8855946
Daniel Yuxuan Ong, Uei Pua

The arc of Buhler (AOB) is a rare anatomical variant. Rupture of an AOB aneurysm is exceedingly rare. In this study, we report a case of AOB aneurysm rupture, which was successfully treated by transcatheter coil embolization. A 74-year-old man presented with symptomatic AOB aneurysm rupture. A computed tomography scan and subsequent angiography revealed the aberrant connection between the common hepatic artery and the superior mesenteric artery. A fusiform AOB aneurysm with focus of active bleeding was detected. This was successfully treated through embolization and sacrifice of the AOB. This suggests that conventional embolization with sacrifice of AOB is a feasible and safe approach.

Buhler弧度(AOB)是一种罕见的解剖变异。AOB动脉瘤破裂极为罕见。在本研究中,我们报告一例AOB动脉瘤破裂,经导管线圈栓塞成功治疗。一名74岁男性表现为有症状的AOB动脉瘤破裂。计算机断层扫描和随后的血管造影显示肝总动脉和肠系膜上动脉之间的异常连接。发现梭状AOB动脉瘤伴病灶活动性出血。通过栓塞和牺牲AOB成功治疗。提示常规栓塞术牺牲AOB是一种可行且安全的方法。
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引用次数: 0
Proptosis with Increased Orbital Fat in an Obese Patient. 1例肥胖患者眼球突出伴眼眶脂肪增加。
Pub Date : 2020-12-08 eCollection Date: 2020-01-01 DOI: 10.1155/2020/8832704
Azhar Seedat, Shaheen Seedat, Sulaiman E I Moosa

Computational tomography (CT) is a well-documented modality in the workup of proptosis. We present a case of proptosis due to increased orbital fat in an obese patient. We review the literature to discuss the most likely causes of increased orbital fat, and we discuss the utility of CT imaging in assessing this pathology.

计算机断层扫描(CT)是一种有充分文献证明的诊断突出的方法。我们报告一例因眼眶脂肪增加而导致眼球突出的肥胖患者。我们回顾文献,讨论眶脂肪增加的最可能原因,并讨论CT成像在评估这种病理中的应用。
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引用次数: 3
期刊
Case Reports in Radiology
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