1. Clinical and imaging characteristics of invasive Klebsiella pneumoniae liver abscess syndrome
Chinese Journal of Medical Imaging Technology 2020;36(8):1202-1206
Objective: To observe the clinical and imaging characteristics of invasive Klebsiella pneumoniae liver abscess syndrome (IKLAS). Methods: Clinical and imaging findings of 18 patients with IKLAS were retrospectively analyzed. Results: Clinical manifestations included fever (n=18), chills (n=11), some accompanied by respiratory, digestive, nervous system symptoms and visual impairment. Among 18 patients, 13 were found with diabetes. Laboratory examinations showed rise of infection indicators and hepatic function abnormality. Liver abscess located at right lobe in 15 cases, at left lobe in 2 cases, simultaneously involved at both right and left lobe in 1 case, sized 2.45-10.27 cm, mean (5.70±2.35)cm, and gas in abscess was observed in 3 cases. Lung lesions mainly located at the peripheral subpleural areas, CT showed nodules without cavity (18/18, 100%), with cavity (15/18, 83.33%) or honeycomb-like (13/18, 72.22%) abscess, with halo sign (4/18, 22.22%), reverse halo sign (3/18, 16.67%), consolidation shadows (3/18, 16.67%), peripheral wedge shadow (2/18, 11.11%), nourishing blood vessels (2/18, 11.11%), ground glass opacity (1/18, 5.56%) and bilateral pleural effusion (15/18, 83.33%). Two patients were found with intracranial and eye infection. Conclusion: IKLAS has certain characteristic imaging manifestations, which are helpful to diagnosis combining with clinical characteristics.
2.Proliferation effects of astragaloside on neural atem cells in vitro
Lijuan CHAI ; Peiru ZHONG ; Zhihuan ZHOU ; Xiuyun WANG ; Ishida TORAO ; Yanjun ZHANG
Chinese Pharmacological Bulletin 1986;0(05):-
Aim To explore the effects of astragaloside(AS)on the proliferation of neural stem cells(NSCs).Methods The NSCs of embryonic day(E)16 SD rat were cultured in vitro.The NSCs were identified by the immunocytochemical(ICC)staining of Nestin.The ICC staining of BrdU was adopted to characterize the proliferation of NSCs.The number of neurospheres and the ICC staining of BrdU were performed to identify their proliferation properties.Real time RT-PCR technique was used to investigate the proliferation mechanisms of the AS on the NSCs.Results Characteristic protein(Nestin)of NSCs labeling,BrdU labeling were positive showed by immunocytochemical staining.The ICC of BrdU labeling results showed that different dosages of AS could promote the proliferation of NSCs in vitro.The proliferation rate of NSCs was increased extremely significant(P
3.A preliminary study of spectral CT parameters in gastrointestinal stromal tumor risk classification
Xueling ZHANG ; Jianhong ZHAO ; Lingyan ZHANG ; Peili ZHANG ; Yanjun CHAI ; Junlin ZHOU
Journal of Practical Radiology 2016;32(12):1880-1883
Objective To evaluate the value of spectral CT in risk classification of gastrointestinal stromal tumor (GIST).Methods Forty-one patients with GIST were collected,including 1 3 in high risk,1 2 in medium risk,1 1 in low risk and 5 in very low risk. All of the patients underwent plain and triple phases contrast enhanced CT with spectral CT scanning mode.CT value of 70 keV monochromatic images,the slope of spectral curve and normalized iodine concentration (NIC)were measured and calculated.Then, data was correlated with the risk of GIST.Results ①The CT value of 70 keV monochromatic images was negative correlation in the arterial phase (r=-0.173),positive correlation in delayed phase (r=0.552),and no correlation in venous phase with the risk of GIST.②The slopes of spectral curves in delayed phase were significantly different in GISTs with the different risk (χ2= 6.641,P= 0.036).③The NIC values of GISTs with different risk were significantly different in the triple phases (F=3.646,χ2=6.046,F=57.233,P=0.035, P=0.049,P<0.001),and correlated with the risk of GIST (r=-0.564)in the delayed phase.Conclusion Quantitative paremeters of spectral CT imaging such as the CT value of 70 keV,the slopes of spectral curves and iodine concentration are valuable for the risk classification of GIST,and can be used as a preoperative reference.
4.Advance in genetics of lissencephaly
Wenxin LIN ; Yingying CHAI ; Guo ZHENG ; Yanjun HUANG
International Journal of Pediatrics 2021;48(11):766-769
Lissencephaly(LIS)is a group of abnormal cerebral cortical dysplasias caused by the defective migration of neurons and it is characterized by thickening of the cerebral cortex, widening of the gyri and disappearance or shallowness of the sulci.Clinically, the patients often have manifestations such as epilepsy, mental retardation, and developmental delay.At present, there is no specific treatment and most patients have poor prognosis.There is currently no specific treatment, and most patients have a poor prognosis.Recently, with the widespreading clinical application of genetic testing, many disease-causing genes related to the lissencephaly have been discovered, so it is important for us to study its pathogenesis and the mode of inheritance.In this study, we reviewed the recent literature on genes associated with lissencephaly.
5.Advance in tic disorder related genes in children
Yingying CHAI ; Wenxin LIN ; Guo ZHENG ; Yanjun HUANG
International Journal of Pediatrics 2022;49(6):389-392
Tic disorders(TD), a complex chronic neuropsychiatric disorder characterized by rapid, involuntary, non rhythmic, single or multiple muscle movements or vocal twitches, usually occurs in children aged from 2 to 15 years.TD has various clinical manifestations, which are usually related to various psychopathology or behavioral comorbidities, including attention deficit hyperactivity disorder, anxiety, depression and obsessive-compulsive disorder.The etiology and pathogenesis of TD are still not completely clear.Immune, genetic, neurobiochemical and environmental factors are generally recognized as factors related to the pathogenesis of TD.In recent years, the research on TD and genetic factors has gradually increased, but so far there is no clear conclusion on the pathogenic genes of TD.This paper only discusses the genes related to TD.