论著

临床特征联合外周血血管内皮生长因子和 α- 羟基丁酸脱氢酶对卵巢癌的诊断价值

Diagnostic value of clinical features combined with peripheral blood vascular endothelial growth factor and α-hydroxybutyrate dehydrogenase levels in ovarian cancer

:77-82
 
        目的   探讨临床特征联合外周血血管内皮生长因子(VEGF)与α-羟基丁酸脱氢酶(α-HBDH)对卵巢癌的诊断价值。方法   选取2022年6月—2024年6月在天津市中心妇产科医院妇科接收的84例卵巢癌恶性肿瘤患者纳入观察组,同期选取84例卵巢良性病变患者纳入对照组。对比两组患者临床资料及VEGF、α-HBDH水平的差异,分析VEGF、α-HBDH水平与卵巢癌恶性肿瘤患者临床特征的相关性。采用二元Logistics回归分析卵巢癌恶性肿瘤的独立危险因素,并采用受试者工作特征(ROC)曲线分析VEGF、α-HBDH水平诊断卵巢癌恶性肿瘤的价值。结果   观察组年龄、身体质量指数(BMI)及血清CA125、HE4、VEGF、α-HBDH水平显著高于对照组(P<0.05),VEGF与α-HBDH水平与国际妇产科联盟(FIGO)分期、分化等级及淋巴结转移均呈正相关关系(P<0.05)。将年龄、BMI、VEGF、α-HBDH作为自变量纳入二元Logistic回归,结果显示BMI、VEGF、α-HBDH是卵巢癌恶性肿瘤的影响因素(P<0.05),ROC曲线分析显示,联合检测VEGF和α-HBDH的AUC达0.921,灵敏度和特异度分别为81.0%和91.7%,优于单独检测(VEGF:AUC=0.702;α-HBDH:AUC=0.796)。结论  BMI联合VEGF与α-HBDH检测可为卵巢癌的诊断提供高效、无创的辅助手段,具有重要临床应用潜力
      Objective  To explore the  diagnostic value of clinical features combined with  peripheral  blood vascular endothelial growth factor(VEGF)and α-hydroxybutyrate dehydrogenase(α-HBDH)levels in ovarian cancer.Methods  A total of 84 patients with malignant ovarian cancer admitted to the gynecology department of Tianjin Central Hospital of Gynecology and Obstetrics from June 2022 to June 2024 were included in the observation group,and 84 patients with benign ovarian lesions during the same period were included in the control group.The clinical data and VEGF,α-HBDH levels of the two groups were compared.Pearson analysis was used to explore the correlation between VEGF,α-HBDH levels,and clinical characteristics of patients with malignant ovarian cancer.Binary Logistic regression analysis was conducted to identify independent risk factors for malignant ovarian cancer,and receiver operating characteristic(ROC) curves were used to analyze the diagnostic value of VEGF and α-HBDH levels for malignant ovarian cancer.Results  The observation group had significantly higher age,BMI,and serum CA125,HE4,VEGF,α-HBDH levels compared to the control group(P<0.05).VEGF and α-HBDH levels were significantly positively correlated with FIGO stage,differentiation grade,and lymph node metastasis(P<0.05).Age,BMI,VEGF,and α-HBDH were included as independent variables in binary Logistic regression,and the results showed that BMI,VEGF,and α-HBDH levelswere independent risk factors for malignant ovarian cancer(P<0.05).ROC curve analysis  revealed that the AUC for combined detection of VEGF and α-HBDH reached 0.921,with sensitivity and specificity of 81.0% and 91.7%,respectively,significantly superior to individual detection(VEGF:AUC=0.702;α-HBDH:AUC=0.796).Conclusions  The detection of BMI combined with VEGF and α-HBDH levels can provide an efficient and noninvasive auxiliary means for the diagnosis of ovarian cancer,which has important clinical application potential.
论著

广州番禺地区鹦鹉热衣原体肺炎的临床特征及疗效分析

Clinical characteristics and treatment efficacy of Chlamydia psittaci pneumonia in Panyu district of Guangzhou

:1574-1580
 
        目的   分析广州番禺地区鹦鹉热衣原体肺炎患者临床表现、实验室及胸部CT特征、并发症以及治疗方案,为其临床诊治提供参考。方法   回顾性分析2022年1月—2024年7月在广州市番禺区何贤纪念医院通过二代测序技术确诊的10例鹦鹉热感染患者的临床资料。结果  5例(5/10)患者有明确的鸟类或禽类接触史,8例(8/10)患者以发热为首发症状,发热(10/10)、咳嗽、咳痰(10/10)、呼吸困难(7/10)、相对缓脉(8/10)是主要临床表现。患者白细胞计数通常正常或轻微升高;多数患者存在有不同程度的电解质紊乱(10/10)及肝功能损伤(8/10)、乳酸脱氢酶升高(8/10),白蛋白显著降低(8/10)和C反应蛋白显著升高(10/10)。最常见的胸部CT异常为多肺叶受累的斑片状或片状实变,而重症患者多合并双侧胸腔积液。大多数患者经四环素或喹诺酮类单用,或者四环素联用β-内酰胺类抗菌药物治疗,预后良好。结论   有鸟类或禽类接触史、以发热为首发或主要症状、存在相对缓脉、白细胞计数升高不明显等临床特征可有助于区分鹦鹉热衣原体肺炎与其他传统细菌性肺炎,但这并不能确诊。二代测序技术是确诊鹦鹉热衣原体感染的很好方法,可以缩短诊断延误时间并改善患者预后。
       Objective  To describe the clinical,laboratory and chest CT characteristics as well as the complications and treatments of Chlamydia psittaci pneumonia patients in Panyu district of Guangzhou,to provide  reference for clinical diagnosis and treatment.Methods  A retrospective study was conducted on the clinical characteristics of Chlamydia psittaci pneumonia patients who were diagnosed by next-generation sequencing in Panyu Hexian Memorial Hospital of Guangzhou form January 2022 to July 2024.Results  Half patients had a definite history of bird or poultry exposure.Fever(100%),cough,sputum(100%),dyspnea(70%),relative bradycardia(80%)were the main clinical presentation.The total white cell counts were usually normal or slightly increased.Most patients had electrolyte disturbance(100%),liver function impairment(80%),lactic dehydrogenase increased(80%),albumin decreased(80%)and C reactive protein increased remarkably(100%).The most common chest CT abnormality was patchy or flaky hyper densities and consolidation,bilateral pleural effusion was common in severe patients.All patient exhibited good recovery after being treated with tetracycline or quinolone alone,or tetracycline in combination with other antibiotics.Conclusions  These characteristics may help distinguish Chlamydia psittaci pneumonia from other traditional bacterial pneumonia,but they are not definitive.Next-generation sequencing may be a promising approach to confirm Chlamydia psittaciinfection,which can shorten the diagnostic delay time and improve the prognosis of patients.
论著

153例住院儿童甲型流感病毒肺炎及混合感染的临床特征

Clinical characteristics of 153 hospitalized children with influenza A virus pneumonia and mixed infection

:1009-1014
 
目的 探讨住院儿童甲型流感病毒肺炎合并其他病原菌感染的临床特征。方法 通过回顾性研究方法,分析2021年6月—2023年6月广州市妇女儿童医疗中心住院治疗的153例甲型流感病毒肺炎患儿的临床资料,针对有无合并其他病原菌感染,分为混合感染组及非混合感染组两组,分别为98例及55例,分析并对比两组的临床特征。结果 甲型流感病毒肺炎患儿以发热、咳嗽、呕吐/腹泻等症状为主,其中混合感染组患儿呕吐/腹泻症状占比高于非混合感染组(P<0.05);两组患儿其他症状及并发症对比差异无统计学意义(P>0.05);儿童甲型流感病毒肺炎患儿检出合并细菌感染的患儿65例(29.41%),合并肺炎支原体感染的患儿33例(21.57%);合并病毒感染的患儿20例(13.07%)。与非混合感染组比较,混合感染组患儿乳酸脱氢酶水平更高,白细胞计数<4×109/L的人数占比更少(P<0.05);其他实验室指标对比差异无统计学意义(P>0.05);经过抗病毒及对症治疗后,150例(98.04%)患儿痊愈出院,3例出现严重并发症,其均伴有其他病原菌感染。与非混合感染组比较,混合感染组患儿住院天数更长、住院费用更高(P<0.05);其他预后指标对比差异无统计学意义(P>0.05)。结论 甲型流感病毒肺炎患儿易感染其他的病原菌,导致疾病治疗难度加大,因此临床要提高警惕,以防混合感染情况发生,尽早采取有效的诊治措施,提高疾病早期治愈率。
Objective To explore the clinical characteristics of hospitalized children with influenza A virus pneumonia complicated with other pathogens.Methods The clinical data of 153 children with influenza A virus pneumonia hospitalized in Guangzhou Women and Children Medical Center in the past two years(June 2021 ~ June 2023)were analyzed retrospectively. According to whether they were infected with other pathogens,they were divided into mixed infection group and non-mixed infection group,with 98 cases and 55 cases respectively.The clinical characteristics of the two groups were analyzed and compared.Results Fever,cough,vomiting and diarrhea were the main symptoms in children with influenza A virus pneumonia,and the proportion of vomiting and diarrhea in children with mixed infection group was higher than that in children without mixed infection group(P<0.05).There was no significant difference in other symptoms and complications between the two groups(P>0.05).There were 65 children(29.41%)with influenza A virus pneumonia and 33 children(21.57%)with mycoplasma pneumonia,20 children(13.07%)with virus infection.Compared with non-mixed infection group,the level of lactate dehydrogenase in children with mixed infection group was higher,and the proportion of children with white blood cell count<4×109/L was less(P<0.05).There was no significant difference in other laboratory indexes(P>0.05).After antiviral and symptomatic treatment,150 cases(98.04%)were cured and discharged,and 3 cases had serious complications,all of which were accompanied by other pathogens.Compared with non-mixed infection group,children in mixed infection group had longer hospitalization days and higher hospitalization expenses(P<0.05).There was no significant difference in other prognostic indicators(P>0.05).Conclusions Children with influenza A virus pneumonia are easily infected with other pathogens,which makes it more difficult to treat the disease.Therefore,we should be vigilant in clinic to prevent mixed infection and take effective diagnosis and treatment measures as soon as possible to improve the early cure rate of the disease.
论著

早产儿坏死性小肠结肠炎的临床特征及危险因素分析

Clinical characteristics and risk factors of necrotizing enterocolitis in premature infants

:1141-1145
 
目的 分析早产儿发生新生儿坏死性小肠结肠炎(NEC)的临床特点及危险因素。方法 选取2021年3月—2023年3月在濮阳市人民医院出生的早产儿160例,根据有无NEC分为NEC组(40例)和非NEC组(120例),总结和比较两组患儿的临床资料,分析早产儿NEC的危险因素。结果 NEC组早产儿的发病时间主要集中在出生后的3~21 d,平均发病时间为(12.84±3.5)d。主要临床症状包括肉眼便血23例(57.5%)、腹胀31例(77.5%)、呕吐18例(45.0%)、呼吸暂停7例(17.5%)、肠穿孔9例(22.5%)。Logistic回归分析发现,败血症、输血、呼吸窘迫综合征及新生儿窒息是早产儿发生NEC的危险因素(P<0.05),而预防应用益生菌以及母乳喂养是NEC的保护因素(P<0.05)。结论 NEC的主要临床表现包括肉眼便血、腹胀、呕吐、呼吸暂停、肠穿孔等;患儿出现NEC与败血症、输血、呼吸窘迫综合征及新生儿窒息等因素相关;母乳喂养和益生菌的应用是其保护因素。
Objective To analyze the clinical characteristics and risk factors of necrotizing enterocolitis(NEC)in premature infants. Methods A total of 160 premature infants born in Puyang People's Hospital from March 2021 to March 2023 were selected and divided into NEC group(40 cases)and non-NEC group(120 cases)according to the presence or absence of NEC.The clinical data were obtained and compared between the two groups.The clinical data of two groups were compared,and the related risk factors of NEC in premature infants were analyzed and summarized. Results The onset time of NEC premature infants is mainly between 3-21 days after birth,with an average onset time of(12.84±3.5)days.The main clinical symptoms included 23 cases(57.5%)of bloody stool,31 cases(77.5%)of abdominal distension,18 cases(45.0%)of vomiting,7 cases(17.5%)of apnea,and 9 cases(22.5%)of intestinal perforation.Logistic regression analysis found that sepsis,blood transfusion,respiratory distress syndrome,and neonatal asphyxia were risk factors for NEC in premature infants(P<0.05),while prophylactic use of probiotics and breastfeeding were protective factors for NEC(P<0.05). Conclusions The main clinical manifestations of NEC include bloody stool,abdominal distension,vomiting,apnea,intestinal perforation,etc.NEC in infants is related to sepsis,blood transfusion,respiratory distress syndrome and neonatal asphyxia.Breastfeeding and the application of probiotics are its protective factors.
论著

YAP、p65与弥漫大B细胞淋巴瘤临床特征的相关性及临床意义

Correlation and clinical significance of YAP and p65 with clinical features of diffuse large B-cell lymphoma

:1389-1396
 
目的 探讨Yes1相关蛋白(YAP)及p65在弥漫大B细胞淋巴瘤(DLBCL)中与临床特征的相关性及对DLBCL治疗和预后的意义。方法 收集65例DLBCL和10例反应性增生淋巴结患者组织进行免疫组织化学染色,分析两组差异;对多种临床特征与YAP、p65的相关性进行统计学和生存差异性分析。结果 YAP、p65染色评分在两组间比较差异有统计学意义(P<0.05);YAP评分与疗效分组呈正相关,与治疗前乳酸脱氢酶(LDH)、Ann-Arbor分期、国际预后指数(IPI)呈负相关(P<0.05);p65表达与疗效分组呈负相关,与治疗前LDH水平、Ann-Arbor分组、美国东部肿瘤协作组活动状态评分(ECOG)ECOG分组、结外侵犯、IPI评分、巨大包块呈正相关(P<0.05)。IPI及p65评分是DLBCL患者总生存期(OS)的独立危险因素(P<0.05)。共表达分层中YAP-/p65+组患者OS均值最低。结论 对于DLBCL,YAP低表达或p65高表达提示患者瘤荷较大、较差的疗效和预后。
Objective To investigate the correlation of YAP and p65 with clinical features in diffuse large B-cell lymphoma(DLBCL)and the significance for treatment and prognosis.Methods Tissues from 65 patients with DLBCL and 10 patients with reactive hyperplasia lymph node were collected for immunohistochemistry staining to analyze the differences between the two groups;statistical analysis and survival difference analysis of the correlation between various clinical features and YAP,p65 were performed.Results YAP and p65 staining scores were significantly different between the two groups(P<0.05).YAP scores were positively correlated with efficacy subgroups,and negatively correlated with LDH levels before treatment,Ann-Arbor staging,and International Prognostic Index(IPI)scores before treatment(P<0.05);p65 expression was negatively correlated with efficacy subgroups,and positively correlated with pretreatment LDH levels,Ann-Arbor subgroup,ECOG subgroup,extra-nodal invasion,IPI scores,and huge mass(P<0.05).IPI and p65 score were independent prognostic risk factors for overall survival(OS) in DLBCL patients(P<0.05).The mean value of OS was the lowest in patients in the YAP-/p65+ group in the co-expression stratification.Conclusions Low expression of YAP or high expression of p65 suggests larger tumor load and poorer outcome and prognosis in patients for DLBCL.
论著

TIMELESS、RAB2A、ASPM在乳腺癌组织中的表达及与临床特征相关性

Expression of TIMELESS,RAB2A and ASPM in breast cancer and their correlation with clinical features

:80-86
 
目的 分析TIMELESS、鼠肉瘤病毒家族相关蛋白2A(RAB2A)、异常纺锤体样小头畸形相关基因(ASPM)在乳腺癌组织中的表达及与临床特征相关性。方法 选取2019年2月—2021年2月我院乳腺癌组织标本84例作为研究组、正常乳腺组织标本53例作为对照组,采用荧光定量聚合酶测定TIMELESS、ASPM,采用Western blot检测RAB2A蛋白表达情况,分析上述三个指标在乳腺癌中表达及与临床特征相关性。结果 对比对照组,研究组TIMELESS、ASPM表达较高,RAB2A较低(P<0.05)。TIMELESS、RAB2A、ASPM与乳腺癌淋巴结浸润、TNM分期、分化程度相关(P<0.05)。TIMELESS、RAB2A、ASPM为影响乳腺癌发生的危险因素(P<0.05)。TIMELESS、RAB2A负相关(r=-0.383、P=0.001);TIMELESS、ASPM正相关(r=0.397、P=0.001);RAB2A、ASPM负相关(r=-0.257、P=0.018)。对比TIMELESS、RAB2A、ASPM单一检测,三者联合检测对乳腺癌的诊断价值较高(P<0.05)。结论 乳腺癌患者TIMELESS、ASPM呈高表达,RAB2A呈低表达,上述三个指标与乳腺癌高度相关,可作为乳腺癌发生的检测指标。
Objective To analyze the expression of TIMELESS,murine sarcoma virus family related protein 2A(RAB2A)and abnormal spindle like microcephaly related gene(ASPM)in breast cancer tissues and their correlation with clinical features.Methods A total of 84 breast cancer tissue samples from our hospital from February 2019 to February 2021 were selected as the study group and 53 normal breast tissue samples were selected as the control group.Time,ASPM and RAB2A protein expression were determined by fluorescent quantitative polymerase,and RAB2A protein expression was detected by Western blot.The expression of the above three indicators in breast cancer and their correlation with clinical characteristics were analyzed.Results Compared with the control group,the study group had higher TIMELESS and ASPM expression levels and lower RAB2A level(P<0.05).TIMELESS,RAB2A and ASPM expressions were correlated with lymph node infiltration,TNM stage and differentiation of breast cancer(P<0.05).TIMELESS,RAB2A and ASPM were the risk factors of breast cancer(P<0.05).TIMELESS and RAB2A were negatively correlated(r=-0.383,P=0.001);TIMELESS and ASPM were positive correlated(r=0.397、P=0.001);RAB2A and ASPM were negatively correlated(r=-0.257,P=0.018).Compared with the single detection of TIMELESS,RAB2A and ASPM,the combined detection had higher diagnostic value for breast cancer(P<0.05).Conclusions Patients with breast cancer had high expression of TIMELESS and ASPM,and low expression of RAB2A.The above three indicators were highly correlated with breast cancer and can be detection indicators for breast cancer.
论著

肺部受累的惠普尔病与初治菌阴肺结核患者的临床特征对比分析

A comparative analysis of the clinical features between patients with pulmonary involvement of Whipple disease and primary treated bacteriological negative pulmonary tuberculosis

:28-33
 
目的 分析对比肺部受累的惠普尔病与初治菌阴肺结核患者的临床特征,提高对肺部受累的惠普尔病的认识、诊断及鉴别水平。方法 回顾性收集20例肺部受累的惠普尔病为病例组,并随机选取同期56例初治菌阴肺结核患者为对照组进行对比,探讨肺部受累的惠普尔病的临床特征。结果 病例组中老年(>37岁)、急性或亚急性的病程比例高于对照组(P<0.05)。CT影像学中,从病灶分布来看,病例组的病灶分布在下叶的病例比例高于对照组(P<0.05),病灶分布在上叶的病例比例低于对照组(P<0.05);从形态上看,病例组中表现为网状病灶、间质性肺炎的比例高于对照组(P<0.05),病例组中表现为空洞、纤维条索、实性影、结节影、树芽征、肺门淋巴结肿大的比例低于对照组(P<0.05),而性别、合并免疫力低下疾病、咳嗽、咳痰、发热、咳血、关节痛、腹泻等在组间比较差异均无统计学意义。病例组全部病例的肺泡灌洗液宏基因测序结果显示:惠普尔养障体是唯一菌19例(95.0%)或主要菌1例(5.00%,合并结核菌1序列),而对照组肺泡灌洗液宏基因测序结果显示:21例(37.5%)检测出结核分枝杆菌(TB)复合群是唯一菌或主要致病菌,18例TB-RNA(+),15例TB-LAMP(+)。结论 惠普尔病在临床可表现为急性或亚急性病程,好发中老年男性,以发热和(或)呼吸道症状为主,可伴或不伴有腹泻、关节痛;肺部影像学以下肺网状、间质性肺炎改变为主,可以单独累及肺部;与初治菌阴肺结核患者临床症状极其相似。应尽快完善支气管镜检查,肺泡灌洗液的宏基因检测对早期、快速诊断此病尤为重要。
Objective To analyze and compare the clinical features of patients with pulmonary involvement of Whipple disease and primary treated bacteriological negative pulmonary tuberculosis,so as to improve the recognition,diagnosis and differentiation ability of pulmonary involvement of Whipple disease.Methods Clinical features of Whipple disease with pulmonary involvement were investigated by retrospectively collecting 20 cases as a case group,comparing with 56 randomly selected patients with primary treated bacteriological negative pulmonary tuberculosis as a control group during the same period.Results The case group had a significantly higher proportion of older patients(>37 years),acute or subacute disease courses than the control group (P<0.05).On CT imaging,in terms of lesion distribution,the proportion of cases with lesions in the lower lobe was significantly more in the case group than in the control group(P<0.05),and the ratio of cases with lesions in the upper lobe was considerably less than in the control group(P<0.05).Regarding morphology,significantly more of the case group showed reticular lesions and interstitial pneumonia than the control group(P<0.05).Significantly fewer of the case group showed cavities,fibrous bands,solid shadows,nodular shadows,tree-bud signs,and enlarged hilar lymph nodes than the control group(P<0.05).No statistically significant differences existed between the two groups in gender,combined immunocompromising diseases,cough,sputum,fever,coughing up blood,arthralgia or diarrhea. At the same time,the differences of gender,combined immunocompromised disease,cough,sputum,fever,coughing up blood,arthralgia,and diarrhea were not statistically significant.The metagenomic sequencing of alveolar lavage fluid in the case group revealed Tropheryma whipplei as the sole pathogenic bacteria in 19 cases(95%)or the primary pathogenic bacteria in 1 case(5.00%,combined TB 1 sequence).In contrast,metagenomic sequencing of alveolar lavage fluid in the control group detected Mycobacterium tuberculosis complex as the sole or primary pathogenic bacteria in 21 cases(37.5%),TB-RNA(+)in 18 cases and TB-LAMP(+)in 15 cases.Conclusions Clinical presentation in Whipple disease can be of an acute or subacute course,preferably in middle-aged and older men,with fever or/and respiratory symptoms,either with or without diarrhea and arthralgia.Its pulmonary imaging dominates with reticular,interstitial pneumonia changes in the lower lungs,which can involve the lungs alone in the disease.At the same time,the clinical symptoms are highly similar to those patients with primary treated bacteriological negative pulmonary tuberculosis.Therefore,it is vital to complete bronchoscopy and metagenomic sequencing of alveolar lavage fluid as soon as possible for early and rapid diagnosis of this Whipple disease.Treatment with sensitive antibacterial drugs can result in significant improvement and save patients' lives.
论著

双下肢乏力伴叶酸缺乏患者临床特征的研究

Study on the clinical characteristics of patients with lower extremity weakness and folic acid deficiency

:22-28
 
目的 总结以双下肢乏力为主要表现的、合并低叶酸血症的患者的临床特征。方法 选择自2017年1月—2020年12月在我院神经内科住院的患者,分为3组:双下肢乏力伴叶酸缺乏组,共23例;叶酸缺乏合并脑血管病组,共129例;叶酸缺乏的健康体检者,为来我院行健康体检、无意中发现叶酸水平降低者,共42例,比较3组患者特征。结果 双下肢乏力伴叶酸缺乏组患者的发病年龄在19~88岁之间,平均(63.82±20.24)岁,男女比为2.3∶1。起病时间(13.34±17.88)d。与叶酸缺乏合并脑血管病组以及与叶酸缺乏的健康体检者相比,双下肢乏力伴叶酸缺乏组患者脑叶缺血灶数量较少,差异有统计学意义,P分别=0.001和0.008;与叶酸缺乏的健康体检者相比,双下肢乏力伴叶酸缺乏组患者放射冠和侧脑室缺血灶数量无变化,差异无统计学意义,P>0.05;与叶酸缺乏合并脑血管病组以及与叶酸缺乏的健康体检者相比,双下肢乏力伴叶酸缺乏组患者整体脑组织缺血灶总数较少,差异有统计学意义,P分别<0.01和0.05。结论 临床上遇到双下肢乏力患者,尤其是发病年龄在63岁左右,男性,起病时间在13 d左右,颅内整体缺血灶、尤其脑叶缺血灶较少的患者,需要警惕低叶酸血症所致双下肢乏力的可能。
Objective To summarize the clinical characteristics of patients with lower extremity weakness as the main manifestation and hypofolicemia.Methods Patients admitted in our neurology inpatient center from January 2017 to December 2020 were selected and divided into 3 groups.Group A consisted of 23 cases of bilateral lower extremity weakness combined with folic acid deficiency.Group B consisted of 129 cases of folic acid deficiency combined with cerebrovascular disease.Group C consisted of 42 healthy people with folic acid deficiency who came to our hospital for health check-up and found that the level of folic acid was decreased accidentally.The clinical characteristics of the three groups of patients were compared.Results The age of onset in group A was between 19 and 88 years old,with an average of(63.82±20.24)years old,and the male to female ratio was 2.3∶1.The onset time was(13.34±17.88)days.Compared with the group B and group C,the number of cerebral lobe ischemic area in group A was lesser,and the difference was statistically significant,P=0.001 and 0.008,respectively.Compared with group C,the number of corona radiata and lateral ventricle ischemic lesions in group A did not change,and the difference was not statistically significant,P>0.05.Compared with group B and group C,the total number of ischemic lesions in the overall brain tissue of group A was lesser,and the difference was statistically significant,P<0.01 and P=0.05 respectively.Conclusions When we encounter patients with bilateral lower extremity weakness in clinical practice,especially the average age of onset is around 63 years old,male,the onset time is about 13 days,and the overall intracranial ischemic lesions,especially the lobar ischemic lesions are less,we need to think of the possibility of bilateral lower extremity weakness caused by hypofolate.
论著

儿童结直肠息肉98例的临床特征及腹腔镜联合结肠镜下手术治疗效果

Clinical characteristics of 98 cases of colorectal polyps in children and the efficacy of laparoscopic surgery combined with colonoscopy

:63-67
 
目的 调查与分析儿童结直肠息肉的临床特征及腹腔镜联合结肠镜下手术对其的治疗效果。方法 选择2019年2月—2021年10月在郑州大学附属儿童医院诊治的98例结直肠息肉患儿,记录患儿的临床特征,根据患儿的手术方法分为腹腔镜组(腹腔镜联合结肠镜下手术治疗,n=40)与结肠镜组(采用结肠镜手术治疗,n=58),对比不同手术方法的治疗效果、并发症发生率、疼痛视觉模拟评分法(VAS)评分、息肉复发与再手术率。结果 98例患儿中,息肉部位为直肠44例、横直肠38例、其他16例;息肉最大直径(1.65±0.24)cm;息肉单发83例、多发15例。腹腔镜组的围手术期指标比结肠镜组改善(P<0.05)。腹腔镜组术后7 d的感染、出血、肠穿孔、肠梗阻等并发症发生率为5.00%,低于结肠镜组的17.24%(P<0.05)。腹腔镜组术后1个月的总有效率为97.50%,高于结肠镜组的82.76%(P<0.05)。腹腔镜组术后1、3、7 d的疼痛VAS评分低于结肠镜组(P<0.05)。所有患儿术后随访1年,联合的息肉复发率与再次手术率为5.00%、2.50%,均低于结肠镜组的18.97%、13.79%(P<0.05)。结论 儿童结直肠息肉主要位于直肠、横直肠,多为单发,腹腔镜联合结肠镜下手术治疗能促进患儿康复,提高总体治疗效果,也能缓解患儿疼痛,减少并发症的发生,降低随访息肉复发率与再次手术率。
Objective To investigate and analyze the clinical features of children with colorectal polyps and the efficacy of laparoscopic surgery combined with colonoscopy. Methods A total of 98 children with colorectal polyps diagnosed and treated in our hospital from February 2019 to October 2021 were selected as subjects of this study. The clinical characteristics of all children were recorded,and they were divided into the laparoscopic group(laparoscopic surgery combined with colonoscopy,n=40)and the colonoscopy group(colonoscopy,n=58)according to the differences in surgical methods. The therapeutic effect,complication rate,VAS pain score,polyp recurrence and reoperation rate of different surgical methods were compared. Results Among the 98 children,the polyps of 44 cases were in rectum,38 cases in transverse rectum and 16 cases in other sites. The maximum diameter of polyp was(1. 65±0. 24)cm. Polyps were solitary in 83 cases and multiple in 15 cases. The perioperative indexes in the laparoscopic group were significantly improved compared with those in the colonoscopy group(P<0. 05). The incidence of postoperative complications such as infection,bleeding,intestinal perforation and intestinal obstruction was 5. 00% in the laparoscopy group,which was significantly lower than 17. 24% in the colonoscopy group(P<0. 05). The total effective rate of laparoscopic group was 97. 50% one month after operation,which was significantly higher than that of colonoscopy group(82. 76%,P<0. 05). The VAS pain score of the laparoscopic surgery group was significantly lower than that of the colonoscopy group at 1,3 and 7 days after surgery(P<0. 05). After 1 year of follow-up,the combined polyp recurrence rate and reoperation rate were 5. 00% and 2. 50%,which were significantly reduced compared with 18. 97% and 13. 79% in colonoscopy group(P<0. 05). Conclusions The main sites of colorectal polyps in children are rectum and transverse rectum,and most of them are solitary. Laparoscopic and colonoscopic surgery for colorectal polyps in children can promote the recovery of children,improve the overall treatment effect of patients,relieve the pain of children,reduce the occurrence of complications,and reduce the recurrence rate and reoperation rate of follow-up polyps in children.
论著

广东省小榄地区急性上消化道出血患者临床特征及其危险因素

Clinical characteristics and risk factors of acute upper gastrointestinal bleeding in Xiaolan District, Guangdong Province

:87-90
 
目的 上消化道出血发作急、变化快,具有较高的危险性,本研究目的在于分析急性上消化道出血患者的临床特征及危险因素,为临床诊治提供参考。方法 将2019年1月—2021年2月年我院的242例疑似急性上消化道出血患者作为研究对象,收集患者的年龄、性别、是否有长期抽烟史、饮酒史,是否有合并症以及并发症等一般资料,运用单因素分析其临床特征,运用多因素Logistic回归分析其独立危险因素。结果 患者年龄、长期饮酒史、消化性溃疡、门脉高压、急性胃黏膜病变、服用阿司匹林(ASA药物)、Hp感染等临床特征与急性上消化道出血具有相关性,与患者的性别、长期抽烟史不具有相关性;年龄、消化性溃疡、门脉高压、服用ASA药物、Hp感染是急性上消化道出血的危险性因素。结论 急性上消化道出血病势程度较重,死亡率高,出血需及时针对性治疗;对于急性上消化道出血高危患者,严密监测病情变化,评估其风险系数。
Objective Upper gastrointestinal bleeding has a high risk because of its rapid change. The purpose of this study is to analyze the clinical characteristics and risk factors of patients with acute upper gastrointestinal bleeding, so as to provide reference for clinical diagnosis and treatment. Methods A total of 242 patients with suspected acute upper gastrointestinal bleeding in our hospital from January 2019 to February 2021 were selected as the research objects. The general data such as patients' age, gender, whether they had a long-term history of smoking or drinking, whether they had complications and data of complications were collected. The clinical characteristics were analyzed by univariate analysis, and the independent risk factors were analyzed by multivariate Logistic regression analysis. Results Age, long-term drinking history, peptic ulcer, portal hypertension, acute gastric mucosal lesions, taking aspirin (ASA drugs), Hp infection and other clinical characteristics were correlated with acute upper gastrointestinal bleeding, but gender and long-term smoking history were not. Age, peptic ulcer, portal hypertension, taking ASA drugs and Hp infection were the risk factors of acute upper gastrointestinal bleeding. Conclusion The acute upper gastrointestinal bleeding is a serious disease, with high mortality, and the bleeding needs timely targeted treatment. For patients with high-risk acute upper gastrointestinal bleeding, closely monitor the changes of the disease and evaluate the risk coefficient are needed.
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