无症状性脑梗塞的CT表现及病因分析

本文说明了无症状性脑梗塞的病灶大小、分布、特点及CT表现。主要病因是动脉粥样硬化、高血压、糖尿病。     

The New Brunswick Health Council at a glance

This article presents an overview of the work of the New Brunswick Health Council (NBHC) since its creation by exploring its mandate and by presenting its different initiatives and publications as they relate to the NBHC's areas of work: population health, care experience, sustainability, and citizen engagement.     

Porokeratosis Causing Change in Melanocytic Nevi

Large cell transformation of mycosis fungoides (MF) is an uncommon phenomenon. We present a case of CD30‐positive large cell transformation and discuss its possible pathophysiology. A 74 year‐old male with a 36‐year history of patch stage MF presented with a 3‐month history of right chest cellulitis that was refractory to IV antibiotic treatment. Skin biopsies from his thigh demonstrated a patchy dermal infiltrate of irregular and hyperchromatic lymphocytes and epidermotropism. The majority of the infiltrate was positive for CD4, CD3, CD2, and negative for CD7. Only 10% were positive for CD25 and CD8. Biopsies obtained from the ulcerated chest nodules showed a dermal infiltrate of large and pleomorphic lymphoid cells with prominent nucleoli. These large lymphoid cells were strongly positive for CD3, CD30, CD25, CD2 and UCHL‐1. Occasional cells were positive for CD4 and CD20. They were negative for ALK‐1, TIA‐1, CD7, CD8, and CD15. T‐gamma receptor gene rearrangement analyses by polymerase chain reaction demonstrated a clonal process with similar rearrangement patterns identified in the patch stage MF as well as in large cell transformation areas. Examinations of his peripheral blood and bone marrow were negative. The patient had tolerated one cycle of CHOP chemotherapy.     

螺旋CT三维成像术-SSD的应用

目的：对三维成像技术SSD的临床应用进行探讨。材料与方法：开展SSD病人20例，其中男13例，女7例，年龄24－69岁，采用西门子Balance CT机，进行容积扫功，层厚2mm-4mm，螺距1－2，三维重建图像后处理采用SSD并采取多个角度观察，分析。结果：20例SSD检查成像良好。结论：SSD是非创伤性影像检查，具有安全、简便、价廉的优点，是一种适合临床广泛应用的影像检查方法。     

纵隔低密度肿块病变CT诊断

目的：提高纵隔低密度肿块病变ＣＴ诊断水平。材料与方法：回顾性分析５１例经临床、手术及病理确诊纵隔低密度肿块变的ＣＴ表现。结果：（１）不同纵隔低密度肿块病变均有其较特定的发病部位;（２）含脂肪密度肿块病变包括囊性畸胎瘤,脂肪瘤 低密度肿块为包括囊性淋巴管瘤,胸腺囊肿,支气管囊肿,心包囊肿,神经纤维瘤囊性变,囊性畸胎瘤,椎旁脓肿;（４）含气及水样密度肿块包括食管癌术后胸腔内胃,食管憩室;（５）２例胸腺     

孤立性肺结节的高分辨CT

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Preclinical PK and PD Studies on 2��-O-Methyl-phosphorothioate RNA Antisense Oligonucleotides in the mdx Mouse Model

Antisense oligonucleotides (AONs) are being developed as RNA therapeutic molecules for Duchenne muscular dystrophy. For oligonucleotides with the 2′-O-methyl-phosphorothioate (2OMePS) RNA chemistry, proof of concept has been obtained in patient-specific muscle cell cultures, the mouse and dog disease models, and recently by local administration in Duchenne patients. To further explore the pharmacokinetic (PK)/pharmacodynamic (PD) properties of this chemical class of oligonucleotides, we performed a series of preclinical studies in mice. The results demonstrate that the levels of oligonucleotides in dystrophin-deficient muscle fibers are much higher than in healthy fibers, leading to higher exon-skipping levels. Oligonucleotide levels and half-life differed for specific muscle groups, with heart muscle showing the lowest levels but longest half-life (~46 days). Intravenous (i.v.), subcutaneous (s.c.), and intraperitoneal (i.p.) delivery methods were directly compared. For each method, exon-skipping and novel dystrophin expression were observed in all muscles, including arrector pili smooth muscle in skin biopsies. After i.v. administration, the oligonucleotide peak levels in plasma, liver, and kidney were higher than after s.c. or i.p. injections. However, as the bioavailability was similar, and the levels of oligonucleotide, exon-skipping, and dystrophin steadily accumulated overtime after s.c. administration, we selected this patient-convenient delivery method for future clinical study protocols.