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Cutaneous Melanoma with Tonsillar Metastasis: Treatment with Cryoablation. 伴有扁桃体转移的皮肤黑色素瘤:冷冻消融治疗。
Q3 Medicine Pub Date : 2022-01-01 Epub Date: 2022-07-25 DOI: 10.15388/Amed.2021.29.1.5
Audrius Dulskas, Mantas Trakymas, Jolita Gibavičienė, Vytautas Čepulis, Agnė Čižauskaitė, Narimantas E Samalavičius

Metastasis of cutaneous melanoma to the oral cavity is a rare condition. Male patient with cutaneous melanoma metastasis to right tonsil 2 years after radical skin lesion resection was treated with surgery: tonsillectomy and later resection of soft palate were performed. Two years later the patient was diagnosed with progressive disease to right tonsil and soft palate. Rapid inoperable relapse was detected six months later. The patient underwent two procedures of palliative cryoablation of the metastasis. Postoperative course was uneventful. Patient died 7 months later due to progression of the disease. Cryoablation alone or together with surgery may be a relatively safe option for treatment of inoperable disease of head and neck tumours.

皮肤黑色素瘤转移到口腔是一种罕见的情况。皮肤黑色素瘤根治术后2年发生右扁桃体转移的男性患者行手术治疗:行扁桃体切除术后软腭切除术。两年后,患者被诊断为右扁桃体和软腭的进行性疾病。6个月后发现无法手术的快速复发。患者接受了两次转移灶的姑息性冷冻消融手术。术后过程顺利。患者7个月后因病情进展死亡。冷冻消融单独或联合手术可能是治疗头颈部肿瘤不可手术疾病的一种相对安全的选择。
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引用次数: 0
Implementation and Evaluation of Preimplantation Genetic Testing at Vilnius University Hospital Santaros Klinikos. 维尔纽斯大学Santaros Klinikos医院植入前基因检测的实施和评估。
Q3 Medicine Pub Date : 2022-01-01 Epub Date: 2022-06-29 DOI: 10.15388/Amed.2022.29.2.9
Eglė Stukaitė-Ruibienė, Živilė Gudlevičienė, Andrė Amšiejienė, Evelina Dagytė, Rimantas Gricius, Kristina Grigalionienė, Algirdas Utkus, Diana Ramašauskaitė

Background and objectives: The most effective treatment of infertility is in vitro fertilization (IVF). IVF with Preimplantation Genetic Testing (PGT) allows to identify embryos with a genetic abnormality associated with a specific medical disorder and to select the most optimal embryos for the transfer. PGT is divided into structural rearrangement testing (PGT-SR), monogenetic disorder testing (PGT-M), and aneuploidy testing (PGT-A). This study mostly analyzes PGT-SR, also describes a few cases of PGT-M. The aim of this study was to implement PGT procedure at Vilnius University Hospital Santaros Klinikos (VUHSK) Santaros Fertility Centre (SFC) and to perform retrospective analysis of PGT procedures after the implementation.

Materials and methods: A single-center retrospective analysis was carried out. The study population included infertile couples who underwent PGT at SFC, VUHSK from January 01st, 2017 to December 31st, 2020. Ion PGM platform (Life Technologies, USA) and Ion ReproSeq PGS View Kit (Life Technologies, USA) were used for the whole genome amplification. Results were assessed using descriptive statistics.

Results: PGT was successfully implemented in VUHSK in 2017. During the analyzed time period, thirty-four PGT procedures were performed for 26 couples. Two procedures were performed in 2017, 7 procedures - in 2018, 13 - in 2019, and 12 - in 2020. In comparison with all IVF procedures, 2.5% procedures were IVF with PGT, a highest percentage was in 2020 (3.8% of all procedures). The main indication for PGT was balanced chromosomal rearrangements (in 85.3% cases). In all 34 cases 515 oocytes were aspirated in total, 309 oocytes were fertilized, oocytes fertilization rate exceeded 60%. A normal diploid karyotype was found in 46 (16.8%) biopsied embryos. Out of all PGT procedures, 9 (26.5%) resulted in a clinical pregnancy. Six (66.7%) pregnancies were confirmed in 2019, and 3 (33.3%) - in 2020. Three (33.3%) pregnancies resulted in spontaneous abortion, 6 (66.7%) - in delivery.

Conclusions: The implementation of PGT in VUHSK was successful. The most common indication for PGT was a reciprocal translocation. Oocytes fertilization rate exceeded 60%, a normal karyotype was found less than in one-fifth of biopsied embryos. A highest clinical pregnancy rate was achieved in 2019 when almost half of women conceived, which is probably related to the experience gained by the multidisciplinary team. This is the first study analyzing IVF with PGT in Lithuania, however, the results should be interpreted with caution due to a low number of total procedures performed.

背景和目的:不孕不育最有效的治疗方法是体外受精(IVF)。植入前基因测试(PGT)的IVF可以识别与特定疾病相关的遗传异常胚胎,并选择最适合移植的胚胎。PGT分为结构重排检测(PGT-SR)、单基因障碍检测(PGT-M)和非整倍体检测(PGT-A)。本研究主要分析PGT-SR,也描述了一些PGT-M的病例。本研究的目的是在维尔纽斯大学Santaros Klinikos医院(VUHSK)Santaros生育中心(SFC)实施PGT程序,并对实施后的PGT程序进行回顾性分析。材料与方法:采用单中心回顾性分析。研究人群包括2017年1月1日至2020年12月31日在VUHSK SFC接受PGT的不孕夫妇。使用Ion PGM平台(Life Technologies,USA)和Ion ReproSeq PGS View Kit(Life Technology,USA)进行全基因组扩增。使用描述性统计对结果进行评估。结果:PGT于2017年在VUHSK成功实施。在分析的时间段内,对26对夫妇进行了34次PGT手术。2017年进行了两次手术,2018年进行了7次,2019年进行了13次,2020年进行了12次。与所有试管婴儿程序相比,2.5%的程序是带PGT的试管婴儿,2020年的比例最高(占所有程序的3.8%)。PGT的主要指征是染色体平衡重排(85.3%的病例)。34例患者共抽吸卵母细胞515枚,受精卵309枚,卵母细胞受精率超过60%。在46个(16.8%)活检胚胎中发现了正常的二倍体核型。在所有PGT手术中,有9例(26.5%)临床妊娠。2019年确认怀孕6例(66.7%),2020年确认怀孕3例(33.3%)。3例(33.3%)妊娠导致自然流产,6例(66.7%)分娩。结论:PGT在VUHSK的实施是成功的。PGT最常见的适应症是相互易位。卵母细胞受精率超过60%,正常核型不到五分之一的活检胚胎。2019年,近一半的女性怀孕,临床妊娠率最高,这可能与多学科团队获得的经验有关。这是立陶宛第一项分析PGT试管婴儿的研究,然而,由于所执行的总程序数量较少,因此应谨慎解释结果。
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引用次数: 0
The Insight into Obstetric Care near the Front Line in Kharkiv. 对哈尔科夫前线附近产科护理的见解。
Q3 Medicine Pub Date : 2022-01-01 Epub Date: 2022-06-29 DOI: 10.15388/Amed.2022.29.2.10
Igor Lakhno

Objectives: The invasion of Russian troops into independent Ukraine has changed the humanitarian situation in the Kharkiv region. The paper is focused on the peculiarities and issues of the management of labor and delivery near the front line.

Materials and methods: Totally 2030 patients were enrolled in the study. 1410 women who delivered in the second half of 2021 were enrolled in Group I. 620 women who delivered in the first half of 2022 were observed in Group II. Some patients from Group II were used for the investigation of the comparative situation during first months of 2022. 85 women who delivered in January were included in Subgroup IIA. 94 women who have completed their pregnancies and delivered in February were observed in Subgroup IIB. 67 case histories of deliveries which occurred during March were united in Subgroup IIC.

Results: The level of anemia, uterine contractile activity in labor abnormalities, and episiotomies were surprisingly lower during wartime in March. The obtained results showed an almost similar level of obstetric complications, maternal comorbidities, and interventions during labor and delivery in all groups. The stressed environment was a possible reason for the elevation of cardiovascular disease and endocrine disorders.

Conclusion: The study did not reveal any significant changes in the structure of maternal pathologies and obstetric complications during the first months of wartime near the front line. But later the levels of cardiovascular disease and endocrine disorders were found to be elevated.

目标:俄罗斯军队入侵独立的乌克兰改变了哈尔科夫地区的人道主义局势。本文着重论述了近一线劳动生产管理的特点和存在的问题。材料和方法:共有2030名患者参与研究。1410名在2021年下半年分娩的女性被纳入第一组。620名在2022年上半年分娩的妇女被纳入第二组。第二组的一些患者被用于调查2022年前几个月的比较情况。一月份分娩的85名妇女被纳入IIA亚组。在IIB亚组中观察到94名已完成妊娠并于2月份分娩的妇女。IIC亚组合并了67例3月份分娩的病例史。结果:在3月份的战争期间,贫血、分娩异常时的子宫收缩活动和会阴的水平出奇地低。所获得的结果显示,所有组的产科并发症、产妇合并症以及分娩和分娩期间的干预措施水平几乎相似。压力大的环境可能是心血管疾病和内分泌紊乱加剧的原因。结论:这项研究没有发现在战争前线附近的头几个月,产妇的病理结构和产科并发症有任何显著变化。但后来发现心血管疾病和内分泌紊乱的水平升高了。
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引用次数: 0
Reproductive Outcome of the Patients with Uterus Unicornis: Five Year Experience in a Tertiary Center. Unicornis子宫患者的生殖结果:在三级中心的五年经验。
Q3 Medicine Pub Date : 2022-01-01 Epub Date: 2022-06-29 DOI: 10.15388/Amed.2022.29.2.14
Sule Atalay Mert, Berna Dilbaz, Ece Sevin Cukurova, Caner Kose, Yaprak Engin Ustun

Aim: The aim is to evaluate the pregnancy outcomes of patients with uterus unicornis for 5-year experience in a tertiary center.

Material and method: Twenty patients with uterus unicornis who were diagnosed with hysterosalpingography and/or 3D TVUSG between 2017 and 2021 and then confirmed with laparoscopy and simultaneous hysteroscopy were recruited into this retrospective study. The reproductive outcome and obstetric complications of the patients were followed up for two years postoperative period.

Results: Overall 20 patients who fulfilled the inclusion criterion were recruited for the study. The mean age was 28.65±5.03 years. Thirteen patients (65%) had primary infertility while the remaining seven had secondary infertility with two of them having a previous ectopic pregnancy. Rudimentary communicating uterine horn was observed in 7 (35%) of the patients. The horns were excised during laparoscopy. Overall, 14 (70%) pregnancies were achieved during the 2 years follow-up period. Twelve (85.7%) patients had a live birth (71.4% term delivery, 21.4% preterm delivery), and two (15.3%) had a first-trimester spontaneous abortion. Six (50%) of 12 patients who had a live birth received tocolytics for preterm labor.

Conclusion: Unicorn uterus is a rare anomaly diagnosed mostly during infertility work-up and might be related to the poor obstetric outcome, but early diagnosis is important for successful pregnancy results for preterm delivery especially in the secondary infertile group. In addition, rudimentary horn excision is recommended due to the high risk of obstetric complications.

目的:目的是评估子宫独角兽患者在三级中心5年的妊娠结局。材料和方法:本回顾性研究招募了20名在2017年至2021年间通过子宫输卵管造影和/或3D TVUSG诊断,然后通过腹腔镜和宫腔镜同时检查确诊的子宫独角兽患者。对患者的生殖结局和产科并发症进行了两年的术后随访。结果:本研究共招募了20名符合入选标准的患者。平均年龄28.65±5.03岁。13名患者(65%)患有原发性不孕,其余7名患者患有继发性不孕,其中2名患者曾发生过宫外孕。在7例(35%)患者中观察到了初步的交通性子宫角。在腹腔镜检查中切除了角。总的来说,在2年的随访期内实现了14例(70%)妊娠。12名(85.7%)患者进行了活产(71.4%为足月分娩,21.4%为早产),2名(15.3%)患者在妊娠早期进行了自然流产。在12名活产患者中,有6名(50%)接受了早产治疗。结论:独角兽子宫是一种罕见的异常,主要在不孕不育检查中诊断出来,可能与产科预后不佳有关,但早期诊断对早产成功妊娠至关重要,尤其是在继发不孕组。此外,由于产科并发症的高风险,建议进行基本的角切除术。
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引用次数: 0
Immunohistochemical Evaluation of BARX1, DLX4, FOXE1, HOXB3, and MSX2 in Nonsyndromic Cleft Affected Tissue. BARX1、DLX4、FOXE1、HOXB3和MSX2在非综合征性Cleft影响组织中的免疫组织化学评价。
Q3 Medicine Pub Date : 2022-01-01 Epub Date: 2022-06-29 DOI: 10.15388/Amed.2022.29.2.13
Mārtiņš Vaivads, Ilze Akota, Māra Pilmane

Background: Nonsyndromic craniofacial clefts are relatively common congenital malformations which could create a significant negative effect on the health status and life quality of affected individuals within the pediatric population. Multiple cleft candidate genes and their coded proteins have been described with their possible involvement during cleft formation. Some of these proteins like Homeobox Protein BarH-like 1 (BARX1), Distal-Less Homeobox 4 (DLX4), Forkhead Box E1 (FOXE1), Homeobox Protein Hox-B3 (HOXB3), and Muscle Segment Homeobox 2 (MSX2) have been associated with the formation of craniofacial clefts. Understanding the pathogenetic mechanisms of nonsyndromic craniofacial cleft formation could provide a better knowledge in cleft management and could be a possible basis for development and improvement of cleft treatment options. This study investigates the presence of BARX1, DLX4, FOXE1, HOXB3, and MSX2 positive cells by using immunohistochemistry in different types of cleft-affected tissue while determining their possible connection with cleft pathogenesis process.

Materials and methods: Craniofacial cleft tissue material was obtained during cleft-correcting surgery from patients with nonsyndromic craniofacial cleft diagnosis. Tissue material was gathered from patients who had unilateral cleft lip (n=36), bilateral cleft lip (n=13), and cleft palate (n=26). Control group (n=7) tissue material was received from individuals without any craniofacial clefts. The number of factor positive cells in the control group and patient group tissue was evaluated by using the semiquantitative counting method. Data was evaluated with the use of nonparametric statistical methods.

Results: Statistically significant differences were identified between the number of BARX1, FOXE1, HOXB3, and MSX2-containing cells in controls and cleft patient groups but no statistically significant difference was found for DLX4. Statistically significant correlations between the evaluated factors were also notified in cleft patient groups.

Conclusions: HOXB3 could be more associated with morphopathogenesis of unilateral cleft lip during postnatal course of the disorder. FOXE1 and BARX1 could be involved with both unilateral and bilateral cleft lip morphopathogenesis. The persistence of MSX2 in all evaluated cleft types could indicate its possible interaction within multiple cleft types. DLX4 most likely is not involved with postnatal cleft morphopathogenesis process.

背景:非综合征性颅面裂是一种相对常见的先天性畸形,可能会对儿科人群中受影响个体的健康状况和生活质量产生重大负面影响。多个裂隙候选基因及其编码蛋白已被描述为可能参与裂隙形成。这些蛋白质中的一些,如同源盒蛋白BarH样1(BARX1)、远端少同源盒4(DLX4)、叉头盒E1(FOXE1)、同源盒蛋白Hox-B3(HOXB3)和肌肉段同源盒2(MSX2),已经与颅面裂的形成有关。了解非综合征性颅面裂形成的发病机制,可以为腭裂的治疗提供更好的知识,并为开发和改进腭裂治疗方案提供可能的基础。本研究通过免疫组织化学方法研究了BARX1、DLX4、FOXE1、HOXB3和MSX2阳性细胞在不同类型的腭裂病变组织中的存在,同时确定了它们与腭裂发病过程的可能联系。材料和方法:在非综合征性颅面裂患者的唇裂矫正手术中获得颅面裂组织材料。组织材料收集自单侧唇裂(n=36)、双侧唇裂(n=13)和腭裂(n=26)患者。对照组(n=7)从没有任何颅面裂的个体接受组织材料。使用半定量计数方法评估对照组和患者组组织中因子阳性细胞的数量。使用非参数统计方法对数据进行评估。结果:对照组和腭裂患者组中含有BARX1、FOXE1、HOXB3和MSX2的细胞数量之间存在统计学显著差异,但DLX4没有发现统计学显著差异。在腭裂患者组中,评估因素之间也存在统计学上显著的相关性。结论:HOXB3可能与单侧唇裂的形态发生机制密切相关。FOXE1和BARX1可能参与单侧和双侧唇裂的形态学发病机制。MSX2在所有评估的裂隙类型中的持续存在可能表明其在多种裂隙类型中可能存在相互作用。DLX4很可能与出生后腭裂的形态发生过程无关。
{"title":"Immunohistochemical Evaluation of BARX1, DLX4, FOXE1, HOXB3, and MSX2 in Nonsyndromic Cleft Affected Tissue.","authors":"Mārtiņš Vaivads,&nbsp;Ilze Akota,&nbsp;Māra Pilmane","doi":"10.15388/Amed.2022.29.2.13","DOIUrl":"https://doi.org/10.15388/Amed.2022.29.2.13","url":null,"abstract":"<p><strong>Background: </strong>Nonsyndromic craniofacial clefts are relatively common congenital malformations which could create a significant negative effect on the health status and life quality of affected individuals within the pediatric population. Multiple cleft candidate genes and their coded proteins have been described with their possible involvement during cleft formation. Some of these proteins like Homeobox Protein BarH-like 1 (BARX1), Distal-Less Homeobox 4 (DLX4), Forkhead Box E1 (FOXE1), Homeobox Protein Hox-B3 (HOXB3), and Muscle Segment Homeobox 2 (MSX2) have been associated with the formation of craniofacial clefts. Understanding the pathogenetic mechanisms of nonsyndromic craniofacial cleft formation could provide a better knowledge in cleft management and could be a possible basis for development and improvement of cleft treatment options. This study investigates the presence of BARX1, DLX4, FOXE1, HOXB3, and MSX2 positive cells by using immunohistochemistry in different types of cleft-affected tissue while determining their possible connection with cleft pathogenesis process.</p><p><strong>Materials and methods: </strong>Craniofacial cleft tissue material was obtained during cleft-correcting surgery from patients with nonsyndromic craniofacial cleft diagnosis. Tissue material was gathered from patients who had unilateral cleft lip (n=36), bilateral cleft lip (n=13), and cleft palate (n=26). Control group (n=7) tissue material was received from individuals without any craniofacial clefts. The number of factor positive cells in the control group and patient group tissue was evaluated by using the semiquantitative counting method. Data was evaluated with the use of nonparametric statistical methods.</p><p><strong>Results: </strong>Statistically significant differences were identified between the number of BARX1, FOXE1, HOXB3, and MSX2-containing cells in controls and cleft patient groups but no statistically significant difference was found for DLX4. Statistically significant correlations between the evaluated factors were also notified in cleft patient groups.</p><p><strong>Conclusions: </strong>HOXB3 could be more associated with morphopathogenesis of unilateral cleft lip during postnatal course of the disorder. FOXE1 and BARX1 could be involved with both unilateral and bilateral cleft lip morphopathogenesis. The persistence of MSX2 in all evaluated cleft types could indicate its possible interaction within multiple cleft types. DLX4 most likely is not involved with postnatal cleft morphopathogenesis process.</p>","PeriodicalId":34365,"journal":{"name":"Acta Medica Lituanica","volume":"29 2","pages":"271-294"},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9799009/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41168447","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Case of Post-COVID-19 Fibrosis Mimicking Thoracic Manifestation of Ankylosing Spondylitis. covid -19后纤维化模拟强直性脊柱炎胸部表现1例。
Q3 Medicine Pub Date : 2022-01-01 Epub Date: 2022-03-29 DOI: 10.15388/Amed.2021.29.1.10
Emrah Doğan, Sabri Serhan Olcay, Tuba Çınar Olcay, Utku Tapan, Ozge Tapan, Fatih Alaşan

The most common thoracic manifestation form of ankylosing spondylitis is apical fibrocystic changes. It is also known as apical fibrobullous disease (AFBD). The patient was diagnosed with ankylosing spondylitis before 9 years. He suffered COVID-19 infection and passed an intensive care period. However, post-covid fibrosis (PCF) atypically affected dominantly apical zones. If we had no sequential CT evaluations, our case could be easily confused with AFBD. On CT taken before COVID-19, the lung apex was normal. Thus, it was confirmed that there was no rheumatologic thoracic manifestation in the patient before suffering from COVID-19 pneumonia. PCF created similar changes as AFBD. Our case is the first reported paper on this topic.

强直性脊柱炎最常见的胸部表现形式是根尖纤维囊性改变。它也被称为根尖纤维大疱病(AFBD)。患者在9年前被诊断为强直性脊柱炎。他感染了新冠肺炎,并度过了重症监护期。然而,covid后纤维化(PCF)非典型地主要影响根尖区。如果我们没有连续的CT评估,我们的病例很容易与AFBD混淆。在COVID-19之前的CT上,肺尖正常。因此,证实患者在患COVID-19肺炎前没有风湿病胸廓表现。PCF产生了与AFBD类似的变化。我们的案例是关于这个主题的第一篇报道。
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引用次数: 0
Vaccination Against COVID-19 Disease During Pregnancy. 怀孕期间预防COVID-19疾病的疫苗接种。
Q3 Medicine Pub Date : 2022-01-01 Epub Date: 2022-07-26 DOI: 10.15388/Amed.2021.29.1.11
Austėja Voiniušytė, Miglė Černiauskaitė, Virginija Paliulytė, Rūta Einikytė, Diana Ramašauskaitė

Background: The effect of COVID-19 disease during pregnancy is still under investigation, however scientific studies have shown that pregnant women with COVID-19 infection are at increased risk for severe illness or complications [1]. Risk factors for severe disease and death in pregnancy include maternal age (especially ≥35 years), obesity, preexisting medical comorbidities (particularly hypertension and diabetes or more than one comorbidity), and being unvaccinated [2]. Many societies of obstetricians and gynecologists recommend that all pregnant patients undergo COVID-19 vaccination [1]. The aim of this study is to observe demographic characteristics, including education, place of residence and type of employment of women who chose to be vaccinated against COVID-19 in Lithuania, as well as to investigate any adverse reactions following the COVID-19 vaccine during pregnancy and compare the results to published scientific data.

Materials and methods: An online questionnaire for pregnant women primarily located in Lithuania who received at least one dose of COVID-19 vaccine before giving birth has been launched in July, 2021. Data were entered via Google Forms and analyzed using Microsoft Excel and IBM SPSS Statistics. Literature review was performed on PubMed and Google Scholar search engines on inclusion criteria: publication date 2019-2021, used keywords pregnancy, COVID-19, vaccination, side effects.

Results: Data were collected from 227 women vaccinated against COVID-19 during pregnancy. It was observed that the most chosen vaccine was Pfizer-BioNTech BNT162b2 (196 out of 227 individuals (86%)). More pregnant women confirmed having fever after the second dose compared to the first dose (p=0.006). In addition, injection site pain was the most common local side effect after both doses (98%) and more common after the first dose compared to the second (p=0.002). Regarding systemic reactogenicity more women experienced fatigue after the second dose comparing to the first dose (p=0.01). Furthermore, more women were unable to engage in daily activities after the second dose (p=0.03). All other symptoms did not differ after doses 1 and 2.

Conclusions: Overall findings of this study did not suggest any obvious safety signals among pregnant individuals who received COVID-19 vaccine and all the side effects were comparable to the general population. Completed literature review indicates that pregnant women vaccinated against COVID-19 experience the same side effects as individuals in general population and no specific postvaccination reactions among pregnant individuals are observed.

背景:COVID-19疾病对妊娠期的影响仍在调查中,但科学研究表明,感染COVID-19的孕妇发生严重疾病或并发症的风险增加[1]。严重疾病和妊娠死亡的危险因素包括产妇年龄(尤其是≥35岁)、肥胖、既往医学合并症(特别是高血压和糖尿病或一种以上合并症)和未接种疫苗[2]。许多妇产科医师协会建议所有妊娠患者接种COVID-19疫苗[1]。本研究的目的是观察立陶宛选择接种COVID-19疫苗的妇女的人口统计学特征,包括教育程度、居住地和就业类型,以及调查怀孕期间接种COVID-19疫苗后的任何不良反应,并将结果与已发表的科学数据进行比较。材料和方法:2021年7月,针对主要位于立陶宛、在分娩前至少接种过一剂COVID-19疫苗的孕妇开展了在线问卷调查。数据通过Google Forms输入,并使用Microsoft Excel和IBM SPSS Statistics进行分析。在PubMed和Google Scholar搜索引擎上进行文献综述,纳入标准为:发表日期2019-2021,关键词妊娠、COVID-19、疫苗接种、副作用。结果:收集了227名怀孕期间接种COVID-19疫苗的妇女的数据。结果发现,选择最多的疫苗是Pfizer-BioNTech BNT162b2(227个人中有196人(86%))。与第一次接种相比,第二次接种后确诊发烧的孕妇较多(p=0.006)。此外,注射部位疼痛是两种给药后最常见的局部副作用(98%),与第二次给药相比,第一次给药后更常见(p=0.002)。关于全身反应原性,与第一次剂量相比,第二次剂量后更多的妇女出现疲劳(p=0.01)。此外,更多的妇女在第二次剂量后无法从事日常活动(p=0.03)。在剂量1和剂量2后,所有其他症状没有差异。结论:本研究的总体结果未提示接种COVID-19疫苗的孕妇有任何明显的安全性信号,所有副作用与一般人群相当。已完成的文献综述表明,接种COVID-19疫苗的孕妇与一般人群的副作用相同,未观察到孕妇接种疫苗后的特定反应。
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引用次数: 0
Jackstone: A Calculus "Toy" in the Bladder. A Case Report of Rare Entity and Comprehensive Review of the Literature. 杰克斯通:膀胱里的微积分“玩具”。罕见实体病例报告及文献综合复习。
Q3 Medicine Pub Date : 2022-01-01 Epub Date: 2022-01-26 DOI: 10.15388/Amed.2021.29.1.6
Evangelos N Symeonidis, Dimitrios Memmos, Anastasios Anastasiadis, Ioannis Mykoniatis, Eliophotos Savvides, Georgios Langas, Panagiotis Baniotis, Athanasios Bouchalakis, Stavros Tsiakaras, Panagiotis Stefanidis, Michail Stratis, Wilbert F Mutomba, Ioannis Vakalopoulos, Georgios Dimitriadis

Background: An uncommon type of urinary calculus, Jackstone was named after its distinct resemblance to the children's game "Jacks." It typically involves the bladder and, to a lesser extent, the upper urinary tract.

Case presentation: Herein, we report a case of Jackstone vesical calculus in a 75-year-old male undergoing elective open prostate surgery for benign prostate hyperplasia refractory to medical treatment. Preoperative clinical examination revealed intermittent gross hematuria and symptoms suggestive of bladder outlet obstruction, while radiological investigation confirmed the presence of a solitary star-shaped spike-like bladder stone along with an overly enlarged prostate. Following open simple prostatectomy and concomitant intact stone removal, our patient made an uneventful postoperative recovery.

Conclusion: This case highlights an infrequent subtype of bladder lithiasis and further expands upon the importance of promptly treating the underlying cause once this rare entity is detected. A comprehensive review of the literature on Jackstone calculi is further presented.

背景:Jackstone是一种罕见的尿路结石,因其与儿童游戏“Jacks”的明显相似而得名。它通常累及膀胱,在较小程度上累及上尿路。病例介绍:在此,我们报告一例75岁男性Jackstone膀胱结石,因良性前列腺增生难治性药物治疗而接受择期开放前列腺手术。术前临床检查显示间歇性肉眼血尿和提示膀胱出口梗阻的症状,而影像学检查证实存在孤立的星形刺状膀胱结石并伴有前列腺过度增大。在开放性单纯前列腺切除术并同时取出完整的结石后,我们的患者术后恢复顺利。结论:本病例强调了膀胱结石的罕见亚型,并进一步说明了一旦发现这种罕见的实体,及时治疗潜在原因的重要性。本文进一步对Jackstone结石的相关文献进行了综述。
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引用次数: 1
Incidentally Diagnosed Extraluminal Leiomyosarcoma of Infrarenal Inferior Vena Cava: A Case Report and Literature Review from a Radiologist's Perspective. 偶然诊断的肾下下腔静脉腔外平滑肌肉瘤:从放射科医生角度的病例报告和文献复习。
Q3 Medicine Pub Date : 2022-01-01 Epub Date: 2022-06-29 DOI: 10.15388/Amed.2022.29.2.12
A Ebinesh, Aanchal Ashta, Satyam, Gaurav Shanker Pradhan, Rohin Sharma, Prince Das

Background: Vascular leiomyosarcoma is a rare but most common vascular tumor of the inferior vena cava.

Case presentation: We present the case of an incidentally diagnosed extraluminal leiomyosarcoma of the inferior vena cava in a 62 year old patient who presented with abdominal pain following blunt trauma. Ultrasonography showed a lobulated hypoechoic lesion in the upper abdomen. Computed tomography (CT) and magnetic resonance imaging (MRI) showed a circumscribed lobulated near homogeneously enhancing retroperitoneal lesion in anterior relation to the infrarenal inferior vena cava, right paramedian in location with imperceptible vena caval lumen at the site of maximum contact. In positron emission tomography (PET) CT the lesion showed mild fluorodeoxyglucose (FDG) uptake with no distant metastases. CT guided biopsy with immunohistochemical analysis showed leiomyosarcoma. Patient underwent surgical resection with inferior vena cava reconstruction.

Conclusions: Leiomyosarcoma of the inferior vena cava is a rare tumor of vascular origin. Imaging plays an imperative role in the diagnosis and preoperative evaluation. This article also provides a comprehensive literature review of the radiological features of inferior vena caval leiomyosarcoma that would aid in optimal preoperative characterization and evaluation.

背景:血管平滑肌肉瘤是一种罕见但最常见的下腔静脉血管肿瘤。病例介绍:我们介绍了一例62岁的患者,偶然诊断为下腔静脉腔外平滑肌肉瘤,该患者在钝性创伤后出现腹痛。超声检查显示上腹部有分叶性低回声病变。计算机断层扫描(CT)和磁共振成像(MRI。在正电子发射断层扫描(PET)CT中,病变显示轻度氟脱氧葡萄糖(FDG)摄取,无远处转移。CT引导下免疫组化活检显示平滑肌肉瘤。患者接受了下腔静脉重建手术切除。结论:下腔静脉平滑肌肉瘤是一种罕见的血管源性肿瘤。影像学在诊断和术前评估中起着至关重要的作用。本文还对下腔静脉平滑肌肉瘤的放射学特征进行了全面的文献综述,这将有助于优化术前特征和评估。
{"title":"Incidentally Diagnosed Extraluminal Leiomyosarcoma of Infrarenal Inferior Vena Cava: A Case Report and Literature Review from a Radiologist's Perspective.","authors":"A Ebinesh,&nbsp;Aanchal Ashta,&nbsp;Satyam,&nbsp;Gaurav Shanker Pradhan,&nbsp;Rohin Sharma,&nbsp;Prince Das","doi":"10.15388/Amed.2022.29.2.12","DOIUrl":"https://doi.org/10.15388/Amed.2022.29.2.12","url":null,"abstract":"<p><strong>Background: </strong>Vascular leiomyosarcoma is a rare but most common vascular tumor of the inferior vena cava.</p><p><strong>Case presentation: </strong>We present the case of an incidentally diagnosed extraluminal leiomyosarcoma of the inferior vena cava in a 62 year old patient who presented with abdominal pain following blunt trauma. Ultrasonography showed a lobulated hypoechoic lesion in the upper abdomen. Computed tomography (CT) and magnetic resonance imaging (MRI) showed a circumscribed lobulated near homogeneously enhancing retroperitoneal lesion in anterior relation to the infrarenal inferior vena cava, right paramedian in location with imperceptible vena caval lumen at the site of maximum contact. In positron emission tomography (PET) CT the lesion showed mild fluorodeoxyglucose (FDG) uptake with no distant metastases. CT guided biopsy with immunohistochemical analysis showed leiomyosarcoma. Patient underwent surgical resection with inferior vena cava reconstruction.</p><p><strong>Conclusions: </strong>Leiomyosarcoma of the inferior vena cava is a rare tumor of vascular origin. Imaging plays an imperative role in the diagnosis and preoperative evaluation. This article also provides a comprehensive literature review of the radiological features of inferior vena caval leiomyosarcoma that would aid in optimal preoperative characterization and evaluation.</p>","PeriodicalId":34365,"journal":{"name":"Acta Medica Lituanica","volume":"29 2","pages":"258-270"},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9799014/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41170289","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Polycystic Horseshoe Kidney: A Rare Coexistence as a Challenge for the Surgeons. Case Report. 多囊马蹄肾:罕见共存对外科医生的挑战。病例报告。
Q3 Medicine Pub Date : 2022-01-01 Epub Date: 2022-06-29 DOI: 10.15388/Amed.2022.29.2.7
Dionysios Prevezanos, Nikolaos Garmpis, Dimitrios Dimitroulis, Anna Garmpi, Vasiliki E Georgakopoulou, Christos Damaskos

Autosomal dominant polycystic kidney disease (ADPKD) with concomitant horseshoe kidney is an extremely rare entity. In this case, we report a 45-year-old male patient with ADPKD and a horseshoe kidney who demonstrated hypertension, urological complications, and discomfort symptoms such as pain, breathing difficulties, and abdominal meteorism. After preoperative assessment and planning, the patient underwent nephrectomy. Bilateral nephrectomy without dividing the isthmus was performed successfully. The isthmus, which had complicated vasculature and was full of cysts, remained intact, avoiding severe bleeding and infection. The postoperative course was uneventful. Keeping the isthmus intact in such cases is a challenge for the surgeon. The rarity of polycystic horseshoe kidney in combination with the altered abdominal anatomy requires the proper preoperative strategy in order to avoid intraoperative complications.

常染色体显性多囊肾病(ADPKD)伴马蹄肾是一种极为罕见的疾病。在这种情况下,我们报告了一名患有ADPKD和马蹄形肾的45岁男性患者,他表现出高血压、泌尿系统并发症和不适症状,如疼痛、呼吸困难和腹部急流勇进。经过术前评估和计划,患者接受了肾切除术。成功地进行了不分割峡部的双侧肾切除术。峡部血管系统复杂,充满囊肿,保持完整,避免了严重出血和感染。术后进展顺利。在这种情况下,保持峡部完整对外科医生来说是一个挑战。多囊马蹄肾的罕见合并腹部解剖结构的改变需要正确的术前策略,以避免术中并发症。
{"title":"Polycystic Horseshoe Kidney: A Rare Coexistence as a Challenge for the Surgeons. Case Report.","authors":"Dionysios Prevezanos,&nbsp;Nikolaos Garmpis,&nbsp;Dimitrios Dimitroulis,&nbsp;Anna Garmpi,&nbsp;Vasiliki E Georgakopoulou,&nbsp;Christos Damaskos","doi":"10.15388/Amed.2022.29.2.7","DOIUrl":"https://doi.org/10.15388/Amed.2022.29.2.7","url":null,"abstract":"<p><p>Autosomal dominant polycystic kidney disease (ADPKD) with concomitant horseshoe kidney is an extremely rare entity. In this case, we report a 45-year-old male patient with ADPKD and a horseshoe kidney who demonstrated hypertension, urological complications, and discomfort symptoms such as pain, breathing difficulties, and abdominal meteorism. After preoperative assessment and planning, the patient underwent nephrectomy. Bilateral nephrectomy without dividing the isthmus was performed successfully. The isthmus, which had complicated vasculature and was full of cysts, remained intact, avoiding severe bleeding and infection. The postoperative course was uneventful. Keeping the isthmus intact in such cases is a challenge for the surgeon. The rarity of polycystic horseshoe kidney in combination with the altered abdominal anatomy requires the proper preoperative strategy in order to avoid intraoperative complications.</p>","PeriodicalId":34365,"journal":{"name":"Acta Medica Lituanica","volume":"29 2","pages":"211-216"},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9799004/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41168461","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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Acta Medica Lituanica
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