ABSTRACT
OBJECTIVE：To opt imize the extraction technology of phenolic acid from Amomum tsaoko . METHODS ：The extraction technology of phenolic acid from A. tsaoko was optimized by using Box-Behnken design-response surface methodology with ethanol volume fraction ，liquid-solid ratio and extraction time as factors ，using the total contents of protocatechuic acid and vanillic acid as response value. The optimizd extraction technology was vlidated. RESULTS ：The optimal extraction technology was as follows ：ethanol volume fraction 65％，liquid-solid ratio 4∶1（mL/g），extraction time 2.5 h. After 3 times of validation tests ， average total content of protocatechuic acid and vanillic acid were 12.32 mg/g（RSD＝0.26 ％，n＝3），average relative error of which with predicted value （12.63 mg/g）was 2.45％. CONCLUSIONS ：The optimal technology is stable and feasible .
ABSTRACT
Objective To investigate the MRI manifestations of pilomyxoid astrocytoma (PMA)at unusual sites and differential diagnosis in children.Methods The clinical and MRI data from 6 cases of PMA with atypical locations confirmed by surgery and pathology were analyzed retrospectively.Results 2 cases located at cerebral hemisphere,1 case at tegmentum mesencephali,1 case at medulla and 2 cases at cerebellar hemisphere.There were 4 cases of solid tumor and 2 case belonged to cystic-solid mass.5 cases were round or oval and 1 case was shallow lobulated.In addition,there were 2 cases with hemorrhage and 2 cases with peritumoral edema.T1WI showed hypointensity,isointense or slightly hyperintense while T2WI and fluid attented inversion recovery (FLAIR)exhibited isointensity or hyperintensity.After contrast administration,there were 3 cases of obvious multi-ring enhancement,of which 1 case showed astral enhancement of the mural nodules and the other 3 cases showed mild homogeneous or inhomogeneous enhancement.4 cases showed non-enhanced areas in the solid parts.No signs of leptomeningeal dissemination were found in all 6 cases.Conclusion The PMA at unuaual sites in children is primarily solid or cystic-solid,and the image manifestations of plain scan are varied.After enhancement,the tumors show obviously multi-circular enhancement and mild homogeneous or inhomogeneous enhancement could be observed,no enhancement areas are visible in the solid parts.It is noteworthy to distinguish this astrocytoma from other lesions.
ABSTRACT
Objective To improve the diagnostic level of the holoprosencephaly (HPE) disease in children by imaging analysis. Methods From May 2007 to August 2015, 14 cases of HPE in children were collected (7 males and 7 females, aged 2 days to 8 years, mean 14 months). Two cases were showed as sucking difficulty and convulsions frequently after birth. Mental and motor development defects were showed in 12 cases, in which 4 cases were associated with cleft lip and palate deformities and 1 case with microcephaly. Of the 14 cases, CT scan was performed in 7 cases and MRI scan in 7 cases. Results All 14 cases were consistent with the diagnostic criteria of HPE according to the imaging findings of literatures reviewed. Four cases were showed as semilobar HPE, 8 cases were lober HPE, and 2 cases were middle interhemispheric fusion variant. There were thirteen cases were associated with corpus callosum agenesis, including 2 cases were with heterotopic gray matter. Putamen and caudate partia fusion were showed in 6 cases, and thalamus partia fusion in 3 cases. One case was associated with schizencephaly, 4 cases were palate malformation, one case was microcephaly, and one case was cerebellar hypoplasia. Conclusion CT and MRI scan could contribute to diagnosis and classification of holoprosencephaly, and determine whether HPE was associated with other neurological abnormalities. MRI scan should be the first choice for HPE diagnosis.
ABSTRACT
Objective To study MRI diagnosis and differential diagnosis of posterior fossa cyst with hydrocephalus in children. Methods MRI performances and clinical data of 56 children with cyst in the posterior fossa and hydrocephalus were analyzed and classified.Results 12 cases of Dandy-Walker malformation(DWM)showed absence of the vermis at different degrees and the enlarged fourth ventricle widely communicating with the large posterior fossa cyst,accompanied by elevation of the tentorium cerebella and hydrocephalus,in which 1 case combined with callosal agenesis,1 case with subependymal gray matter heterotopia and 1 case with subependymal gray matter heterotopia and small occipital encephalocele.9 cases of Blake's pouch cyst(BPC)showed mildly dilatation of the fourth ventricle,and the cyst was below the cerebellar and hydrocephalus.Neither cerebellar hypoplasia nor elevation of the tentorium cerebella was observed. The postirior wall of the cyst was observed on sagittal T 2WI in 5 cases.The choroid plexus of the fourth ventricular moving to the top wall of the cyst were seen on thin sagittal T 2WI in 1 case.35 cases of arachnoid cyst(AC)showed aggregation of cerebrospinal fluid,and the fourth ventricular and aqueductal stenosis at different degrees and hydrocephalus.Conclusion MRI has evident advantages at diagnosis and differential diagnosis of cystic malformations of the posterior fossa with hydrocephalus,especially on sagittal MRI.
ABSTRACT
Objective To explore the clinical and imaging features of pulmonary embolism (PE)in children with mycoplasma pneumonia (MP).Methods The clinical features,imaging manifestations and laboratory data of 6 children with MP complicated by PE were reviewed retrospectively.Results 6 cases of children were admitted with chief complaints of fever and cough,the D-dimer levels were increased obviously.Consolidation was observed in 4 cases in the right lower lobe combined with pleural effusion and in 2 cases in the left lobe,which showed homogeneous enhancement.Filling defect of pulmonary artery was observed in 1 case,and other 5 cases showed sparse pulmonary vascular in consolidation area.D-dimer returned to normal level and consolidation was absorbed after anticoagulation therapy.Conclusion MP combined with PE in children is rare,and the positive detection rate of pulmonary artery angiography is low.PE should be considered when MP continues to deterioration after anti-infection treatment,even though there is no typical imaging findings of PE.
ABSTRACT
Objective To explore the clinical and imaging features of pulmonary embolism (PE)in children with mycoplasma pneumonia (MP).Methods The clinical features,imaging manifestations and laboratory data of 6 children with MP complicated by PE were reviewed retrospectively.Results 6 cases of children were admitted with chief complaints of fever and cough,the D-dimer levels were increased obviously.Consolidation was observed in 4 cases in the right lower lobe combined with pleural effusion and in 2 cases in the left lobe,which showed homogeneous enhancement.Filling defect of pulmonary artery was observed in 1 case,and other 5 cases showed sparse pulmonary vascular in consolidation area.D-dimer returned to normal level and consolidation was absorbed after anticoagulation therapy.Conclusion MP combined with PE in children is rare,and the positive detection rate of pulmonary artery angiography is low.PE should be considered when MP continues to deterioration after anti-infection treatment,even though there is no typical imaging findings of PE.
ABSTRACT
Objective To evaluate the imaging features and causes of cerebral cortical laminar necrosis(CLN) in children,to improve understanding this sign.Methods The imaging and clinical data of 33 children diagnosed with CLN were analyzed retrospectively.The imaging features of CT and MRI were summarized and compared according to their etiologies.Results Children cerebral CLN involved multiple lobes of bilateral hemicerebrum, including the cortical region, subcortical region and basal ganglia region, and linear or gyral shape,patchy shape and punctate shape abnormal density or signal were demonstrated.The typical imaging features were high-signal intensity over the lateral cortical surfaces or along the gyri on T1WI and FLAIR.Diffusion weighted imaging(DWI) showed high signal with restricted diffusion on acute-stage, and Gd-DTPA enhancement demonstrated linear or gyrate enhanced appearance on early-stage.The extent of CLN of cerebral infarction was relatively limited.Acute anoxic encephalopathy showed an early imaging change and extensive involvement.While chronic anoxic encephalopathy and inflammatory encephalopathy showed a late imaging change and a longer existence.Conclusion Children cerebral CLN may have various causes and imaging features,and show characteristic chronological signal changes on imaging studies.The different causes result in the different patterns for CLN in distribution and time distribution.
ABSTRACT
Objective To study the value of MRI and proton magnetic resonance spectroscopy(H 1-MRS)for neonatal hypoxic-is-chemic encephalopathy(HIE).Methods Magnetic resonance imaging (MRI)and proton magnetic resonance spectroscopy (H 1-MRS)were performed in 30 cases of full-term neonates with HIE,and 10 infant control group without evidence of birth asphyxia. Cerebral MRI and H 1-MRS were performed within 1 5 days after birth.The results of H 1-MRS such as subwave crest values of me-tabolites in lesion areas were recorded.The data were analyzed statistically.Results (1)MRI showed abnormal fetures of HIE such as diffuse cerebral edema,loss of hyperintensity in the posterior limb of the internal capsule on T1 WI,gyrus sign,diffuse parenchy-mal hemorrhage,which could predict the severity of brain damage.(2)On H 1-MRS,the ratio of Lac/Cr in HIE group was much higer than that in control group,which was statistically significant (P <0.05).The ratio of Lac/Cr showed a rising trend with clini-cal grading of HIE.The ratio of NAA/Cr and NAA/Cho were lower in HIE group than that in control group (P <0.05),which showed a trend of gradually reduce with clinical grading of HIE.The difference between ratio of Glx-α/Cr in HIE group and control group was also significantly,the moderate-severe group was much higher than the mild group and control group.There was no sig-nificant difference in the ratio of Cho/Cr between the 4 groups.Conclusion The combination of MRI and H 1-MRS can objectively re-flect brain morphology and metabolic changes of HIE,and evaluate the severity of the brain injury,and provide an effective evidence for clinical diagnosis and treatment.
ABSTRACT
Objective To investigate MRI findings and its relationship with clinical grading and prognosis of infant muggy syn-drome (IMS).Methods Twenty five cases of IMS diagnosed newly and nine cases of IMS with follow-up were collected.MRI find-ings were retrospectively analyzed and compared with their clinical data.Results Seven early abnormal signs could be shown on cer-ebral MRI examination.There was no correlation between the clinical grading and three abnormal signs,which were subdural effu-sion,supratentorial cerebral edema and subarachnoid hemorrhage (P >0.05).In contrast,the other four abnormal signs (abnormal signal of subcortex and cortex,diffuse cerebral hemorrhage,basal ganglia and corpus callosum edema or infarction,large area cere-bral infarction)were closely related to the severity of clinical symptom (P <0.05).MRI findings had certain correlation with clinical classification.Conclusion MRI can objectively reflect the serious change of brain damage in IMS,and provide important information for clinical therapy and prognosis.