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The Internet Journal of Radiology最新文献

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Relationships 的关系
Pub Date : 2020-12-22 DOI: 10.4324/9781003087007-3
Daniell Miller, Don Slater
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引用次数: 0
Conclusions 结论
Pub Date : 2020-12-22 DOI: 10.4324/9781003087007-1
Daniell Miller, Don Slater
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引用次数: 0
Being Trini and Representing Trinidad 作为特里尼,代表特立尼达
Pub Date : 2020-12-22 DOI: 10.4324/9781003087007-4
Daniel W. Miller, D. Slater
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引用次数: 0
Religion 宗教
Pub Date : 2020-12-22 DOI: 10.4324/9781003087007-7
Daniell Miller, Don Slater
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引用次数: 0
The Political Economy of the Internet 互联网的政治经济学
Pub Date : 2020-12-22 DOI: 10.5040/9781474215701.ch-005
Daniel W. Miller, D. Slater
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引用次数: 18
Doing Business Online 网上经商
Pub Date : 2020-12-22 DOI: 10.4324/9781003087007-6
Daniel W. Miller, D. Slater
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引用次数: 0
Trinidad and the Internet – An Overview 特立尼达和互联网-概述
Pub Date : 2020-12-22 DOI: 10.4324/9781003087007-2
Daniel W. Miller, D. Slater
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引用次数: 0
Supernumerary Kidney (Triple Kidney) With Horseshoe Component: A Case Report. 马蹄形多肾(三肾)1例。
Pub Date : 2013-01-03 DOI: 10.5580/2ce7
A. Adekanmi, O. Atalabi, I. Ukachukwu
Supernumerary kidney is a rare congenital anomaly of the urinary system with less than 100 cases documented in literatures worldwide. Very rarely documented is the fused supernumerary kidney and horseshoe component with unknown incidence, due to the rarity of this complex anomaly. We hereby present a rare case of complex renal anomalies of fused supernumerary kidneys with horseshoe component misdiagnosed as an abdominal tumour on ultrasound, incidentally discovered at Computed Tomography. Introduction Supernumerary kidneys are rare congenital anomaly of the urinary system with less than 100 cases documented in literatures worldwide. The true incidence is unknown due to the rarity of the anomaly and it is believed to be found in both sexes with equal frequency . Embryologically, supernumerary kidney is believed to results from abnormal division of the nephrogenic cord into two metanephric blastemas that eventually form two kidneys with partial or duplicated ureteral bud 3, this occurs during the period of urogenital system formation about the 5 to 7week of gestation. No racial predominance is documented in the literature. And most cases of supernumerary kidneys are discovered incidentally Diagnosis and treatment are commonly challenging due to the rarity of this anomaly, its varied presentation and sparse documentation in literatures . Though horseshoe kidneys are relatively common renal fusion anomaly with an incidence of about one in 400-800 live births. Coexisting supernumerary and horseshoe kidney are however very rarely documented
多肾是一种罕见的泌尿系统先天性异常,在世界范围内文献记载的病例不足100例。由于这种复杂异常的罕见性,很少有文献记载的合并多生肾和马蹄部分的发病率未知。我们在此报告一例罕见的合并多生肾合并马蹄成分的复杂肾脏异常,在超声上误诊为腹部肿瘤,在计算机断层扫描中偶然发现。摘要多肾是泌尿系统罕见的先天性异常,在世界范围内文献记载的病例不足100例。由于这种异常的罕见性,真正的发病率尚不清楚,据信在两性中发现的频率相同。胚胎学上,多肾被认为是由于肾原索异常分裂为两个后肾母细胞,最终形成两个肾和部分或重复输尿管芽3,这种情况发生在妊娠5至7周左右的泌尿生殖系统形成时期。在文献中没有种族优势的记载。多数病例是偶然发现的,诊断和治疗通常具有挑战性,因为这种异常罕见,其表现多样,文献记载稀少。虽然马蹄肾是相对常见的肾融合异常,发生率约为400-800活产1例。然而,马蹄肾和多余肾共存的情况很少有记载
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引用次数: 2
Soft Tissue Tumors Around The Knee Joint 膝关节周围软组织肿瘤
Pub Date : 2012-05-21 DOI: 10.5580/2ca8
P. Chatra
Knee joint is a common site for many of the soft tissue tumors. Lipoma and hemangioma are the most common. Knowledge of individual tumors is of utmost importance in differentiating one from the other as each tumor demands unique management. MRI is the imaging modality of choice as it best characterizes the soft tissue. In this pictorial essay we describe morphology, imaging findings and clinical significance of each of the soft tissue tumors.
膝关节是许多软组织肿瘤的常见部位。脂肪瘤和血管瘤是最常见的。个体肿瘤的知识是最重要的区分一个从其他的肿瘤,因为每个肿瘤需要独特的管理。MRI是首选的成像方式,因为它最能表征软组织。在这篇图画文章中,我们描述了每种软组织肿瘤的形态学、影像学表现和临床意义。
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引用次数: 0
CJD: A Case Report CJD:病例报告
Pub Date : 2012-05-21 DOI: 10.5580/2c9a
Neema Agarwal, S. Agarwal
Creuzfeldt-Jakob’s Disease (CJD) is a rare neurodegenerative disorder that is included among the transmissible spongiform encephalopathies. The clinical features are those of a rapidly progressive dementia with myoclonic jerks culminating in death in less than one year. We intend to highlight the role of the magnetic resonance imaging (MRI) as a vital tool for the presumptive in vivo diagnosis, thereby obviating the need of histopathologic confirmation of the disease.
克雅氏病(CJD)是一种罕见的神经退行性疾病,是传染性海绵状脑病之一。临床特征是快速进行性痴呆伴肌阵挛痉挛,最终在不到一年的时间内死亡。我们打算强调磁共振成像(MRI)作为假定体内诊断的重要工具的作用,从而消除了对疾病的组织病理学确认的需要。
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引用次数: 0
期刊
The Internet Journal of Radiology
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