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Sun J.,Beijing Aviation General Hospital | Feng S.-H.,Beijing Aviation General Hospital
International Journal of Ophthalmology | Year: 2011

AIM: To compare the change of intraocular pressure (IOP) and correlative factors in exfoliation syndrome combined with cataract and senile cataract 2 years after phacoemulsification. METHODS: A total of 49 patients 54 eyes with exfoliation syndrome combined with cataract underwent phacoemulsification and intraocular lens (IOL) implantation. Based on IOP, they were divided into exfoliation syndrome combined with cataract (XFS) sub-group (29 cases 31 eyes) and exfoliation syndrome combined with cataract and glaucoma (XFG) sub-group (20 cases 23 eyes). 134 senile cataract patients 152 eyes received phacoemulsification and IOL implantation and were selected as a control at the same period; according to IOP, they were divided into cataract group (86 cases 93 eyes) and cataract combined with open angle glaucoma sub-group (48 cases 59 eyes). The exfoliation syndrome combined with cataract group and control group underwent surgery after IOP was normal by medication and the change of IOP was compared within 2 years after phacoemulsification. RESULTS: preoperative IOP of exfoliation syndrome subgroup was higher than that of the control group (21.85±2.23mmHg vs 18.62±3.12mmHg, P=0.002). Two years after phacoemulsification, IOP lowered in both groups (17.60±3.23mmHg vs 15.08±3.18mmHg, P=0.0037). Statistical analysis showed that it was related with surgical perfusion. IOP of XFG group had significantly decreased. CONCLUSION: The exfoliation syndrome combined with cataract group have significantly lower IOP than the control group 2 years after phacoemulsification. Source

Zhang L.,Chinese PLA General Hospital | Jia Z.,Beijing Aviation General Hospital | Mao F.,Chinese Academy of Sciences | Mao F.,University of Chinese Academy of Sciences | And 3 more authors.
Oncology Reports | Year: 2016

Clear cell sarcoma (CCS) is a rare,low-grade carcinoma commonly located in the distal extremities of young adults involving tendons and aponeuroses. CCS is characterized by its poor prognosis due to late diagnosis,multiple local recurrence,propensity to late metastases,and a high rate of tumor-related mortality. The genetic cause for CCS is thought to be EWSR1 gene translocation. However,CCS lacking a translocation may have other,as yet uncharacterized,genetic mutations that can cause the same pathological effect. A combination of whole-exome sequencing and Sanger sequencing of cancer tissue and venous blood from a patient diagnosed with CCS of the salivary gland revealed a somatic missense mutation,c.1061C>T (p.P354L),in exon 9 of the Nibrin gene (NBN). This somatic missense mutation led to the conversion of proline to leucine (p.P354L),resulting in deleterious effects for the NBN protein. Multiple-sequence alignments showed that codon 354,where the mutation (c.1061C>T) occurs,is located within a phylogenetically conserved region. In conclusion,we here report a somatic missense mutation c.1061C>T (p.P354L) in the NBN gene in a patient with CCS lacking an EWSR1-ATF1 fusion. Our findings broaden the genotypic spectrum of CCS and provide new molecular insight that should prove useful in the future clinical genetic diagnosis of CCS. Source

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