1.Effects of T2-FLAIR sequence under different imaging conditions on the appearance of ivy sign in patients with moyamoya disease
Wenxue TIAN ; Shen GAO ; Xiangyun RONG ; Zhaoxue ZHANG ; Jianming CAI ; Fugeng SHENG ; Hongtao ZHANG
Military Medical Sciences 2025;49(4):303-306
Objective To investigate the effect of T2-fluid attenuated inversion recovery(T2-FLAIR)sequence on the appearance of ivy sign in patients with moyamoya disease under different imaging conditions.Methods Coronal T2-FLAIR scans were performed in 51 consecutive adult patients with moyamoya disease who had not undergone surgery and had their first visit to this hospital between March and July of 2024.According to the scanning conditions,the patients were divided into 19 and 14 of the echo train length in two groups,and 103,144,and 195 ms of the time of echo(TE)in three groups,respectively.The left and right cerebral hemispheres and whole brains were scored according to the cerebral vascular anatomy,and scores of the ivy sign of left and right cerebral hemispheres and whole brain were compared.Results There was no statistical significance in the ivy sign scores of right and left cerebral hemispheres and whole brain between the two groups with 19 and 14 of the echo train length(P>0.05).Comparison of ivy sign scores in right and left cerebral hemispheres and whole brain was statistically significant among the three groups of TE at 144,103 and 195 ms(P<0.05).Conclusion The best appearance of ivy sign in patients with moyamoya disease is seen under the condition of TE at 195 ms,so appropriately extending the TE time is helpful for ivy sign display.
2.A new classification of left apicoposterior segmental bronchus and its clinical significance
Jian LIU ; Li WEI ; Li ZHU ; Shuai HU ; Tian XIA ; Wenxue WEI
Chinese Journal of Clinical Thoracic and Cardiovascular Surgery 2024;31(01):92-98
Objective To analyze a new classification of the left apicoposterior segmental bronchus and summarize its clinical significance. Methods We accessed the computed tomography imaging data of the inpatients treated in the Department of Thoracic Surgery, Henan Provincial People's Hospital between January and November 2021. We observed and classified the branching pattern of the left apicoposterior segmental bronchus (B1+2) using three-dimensional computed tomography bronchography and angiography (3D-CTBA) technique. And we filtered out the patients who underwent thoracoscopic left apicoposterior segmentectomy and analyzed their clinical data retrospectively to summarize the instructing significance of different bronchial classification in the accurate and safe operation of left apicoposterior segmentectomy. Results Finally 240 patients were collected, including 131 males and 109 females with a median age of 51.0 (19.0-77.0) years. The anatomical pattern of the left apicoposterior segmental bronchus was divided into four main types based on the branching pattern of the outer subsegmental bronchi (B1+2c): type Ⅰ 10% (24 patients), type Ⅱ 54% (130 patients) , type Ⅲ 17% (40 patients) , type Ⅳ 18% (43 patients) and other variations 1% (3 patients). Thirty-two patients smoothly underwent thoracoscopic left apicoposterior segmentectomy, including 23 patients of type Ⅰ and type Ⅱ receiving LS1+2 resection, the other 9 patients of type Ⅲ and type Ⅳ receiving LS1+2 resection (3 patients), LS1+2c resection (4 patients) and LS1+2(a+b) resection (2 patients). Conclusion This new classification systematically and concisely elucidates the branching characteristics of the left apicoposterior bronchus. Different branching types are instructive to the left apicoposterior segmentectomy.
3.Study on syndromic deafness caused by novel pattern of compound heterozygous variants in the CDH23 gene
Bei CHEN ; Sen ZHANG ; Yongan TIAN ; Huanfei LIU ; Danhua LIU ; Xia XUE ; Ruijun LI ; Xinxin HU ; Jingyuan GUAN ; Wenxue TANG ; Hongen XU
Chinese Journal of Otorhinolaryngology Head and Neck Surgery 2020;55(9):822-829
Objective:To explore the pathogenic variants of a family with syndromic deafness by high-throughput sequencing.Methods:The family was from Puyang City, Henan Province, and had four members, including two with syndromic deafness. The proband and his sister had congenital deafness, and their parents had normal phenotypes. The clinical phenotype of the family was characterized using clinical examinations and pedigree analysis. The clinical examinations included imaging examination, audiometry (pure tone audiometry, acoustic immittance, brainstem auditory evoked potential, and otoacoustic emission), vestibular function test, and ophthalmic examination (visual acuity test, visual field test, fundus examination, visual evoked potential, and electroretinogram). Target exome sequencing of 129 known deafness genes and bioinformatics analysis were used to screen suspected pathogenic variants. Sanger sequencing and minigene assay were used to verify and functionally investigate the mutation detected, respectively. According to the standards and guidelines for interpreting genetic variants proposed by the American College of Medical Genetics and Genomics, the variants c.6049G>A and c.8699A>G were classified as pathogenic/likely pathogenic, and the variant c.9856C>G was classified as variants of uncertain significance.Results:The probands and his sister had severe sensorineural hearing loss with decreased binocular vision, night blindness, decreased peripheral visual field sensitivity and partial visual field defect, and normal vestibular function. Both of them had three CDH23 mutations, including CDH23 (NM_022124.5) c.6049G>A (p.Gly2017Ser),c.9856C>G (p.His3286Asp), and c.8699A>G (p. Asp2900Gly), The first two were inherited from the father, and the last one was from the mother. The missense variants c.9856C>G and c.8699A>G were not included in the gnomad database. The missense mutation c.6049G>A was located in the last position of exon 46 and was predicted to affect splicing by bioinformatics software. The minigene experiment showed that the mutation cause exon skipping of exon 46, resulting in an abnormal protein. Conclusions:Compound heterozygous variations of the CDH23 are the leading cause of USH1D in the family. This study confirms that the compound heterozygosity of splicing and missense variants of the CDH23 gene could lead to USH1D.
4.Pulmonary fibroleiomyomatous hamartoma: report of a case.
Zhenying YUE ; Yanguang DONG ; Zhaojian TIAN ; Songbo ZHAO ; Wenxue LI
Chinese Journal of Pathology 2015;44(12):914-915
Hamartoma
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pathology
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Humans
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Lung Neoplasms
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pathology
5.Pulmonary Fungal Infection in Mid-later Stage after Liver Transplantation
Hong CHEN ; Qing ZHANG ; Wenxue ZHANG ; Yan TIAN ; Fengling ZHAO ; Xu WANG
Chinese Journal of Nosocomiology 2009;0(16):-
-?-D-glucan test.CT finding indicated the pulmonary nodules or masses in 9 cases.Plaque and flocculation lesion found in 3 cases.Ten cases were treated,in which 8 cases were cured,1 case was improved,1 case was dead.The effective rate was 90%,the curative rate was 80%,and the mortality rate was 8.3%.The two cases without treatment were stable.CONCLUSIONS The leading etiologic species of pulmonary fungal infections in the mid-later stage after liver transplantation are Aspergillus and Cryptococcous.It is different between early stage and mid-later stage after liver transplantation on clinical feature,outcome and anti-fungal medicine tolerability.

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