ABSTRACT
[Objective]To investigate the diagnostic characteristics of optic chiasm-hypothalamic glioma (OCHG) and the reasons for its high misdiagnosis rate.[Methods]Retrospective analysis was performed on the clinical features and imaging findings of 32 patients with OCHG,admitted to our hospitals from October 1999 to December 2011 and proved by pathology.Being compared with those features of other diseases in the sellar region,the reasons for high misdiagnosis rate of OCHG were analyzed.[Results] Among the 32 patients,18 were diagnosed correctly before surgery.However,in the other 14,lesions were misdiagnosed as craniopharyngioma in 8,germ cell tumor in 4,pituitary adenoma in 1,and chordoma in 1 with a total misdiagnosis rate reaching 43％.All patients suffered craniotomy surgery for tumor removal.Among the 4 patients misdiagnosed as having germinoma,2 underwent preoperative radiotherapy and 2 performed preoperative EP regimen chemotherapy.According to the features of the CT and MR images,the OCHG were divided into 3 presentations:solid,solid and cyst mixture and round enhanced tumors.The solid lesions (n=10) were easily misdiagnosed as germinoma (4/10,40％);however,the round enhanced tumors (n=5),especially combined with huge calcification (n=4),were extremely easily misdiagnosed as craniopharyngioma (4/5,80％ ).[Conclusion] Comprehensive understanding the growth and image features of OCHG and summing up the misdiagnosis points when comparing to the other diseases in the sellar region are indispensable in improving the presurgical diagnosis accuracy for OCHG.
ABSTRACT
Objectives To investigate the relationship between single nucleotide polymorphism (SNP)H558R in SCN5A gene and chronic Keshan disease (KSD) complicated with hypertension,and the relationship between H558R and occurrence of arrythmia in chronic KSD complicated with hypertension.MethodsThirty nine patients with chronic KSD complicated with hypertension and 63 geographical region matched hypertension control subjects were recruited in our study in Fuyu county,Qiqihaer city,Heilongjiang province between 2006 and 2010.H558R polymorphism in case and control groups was genotyped using the polymerase chain reaction single-strand conformation polymorphism(PCR-SSCP) and sequenced,and electrocardiography(ECG) characteristics were examined in the two groups.Case-control study analytical methods were applied to analyze the relationship between H558R and chronic KSD complicated with hypertension,and the relationship between H558R and occurrence of arrythmia in chronic KSD patients complicated with hypertension.Results Subjects of genotype 558 TC in the case group had a decreased risk of chronic KSD complicated with hypertension with odds ratio of 0.288[95％ confidence interval (CI):0.104 - 0.794],and subjects of genotype TC in chronic KSD complicated hypertension patients had a decreased risk of QRS prolongation with odds ratio of 0.061 (95％CI:0.006 - 0.612).Conclusions Polymorphism H558R in SCN5A gene may be a predisposition factor of chronic KSD complicated with hypertension and occurrence of arrythmia in chronic KSD complicated with hypertension.