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The Assessment of CDX1, IHH, SHH, GATA4, FOXA2, FOXF1 in Congenital Intra-Abdominal Adhesions CDX1、IHH、SHH、GATA4、FOXA2、FOXF1 对先天性腹腔内粘连的评估
Q3 Medicine Pub Date : 2024-05-22 DOI: 10.15388/amed.2024.31.1.15
Helēna Freijere Pope, M. Pilmane, Anna Junga, A. Petersons
Congenital abdominal adhesions are a rare condition that can result in a small bowel obstruction at any age, more frequently in pediatric populations. The cause remains unknown, and the importance of aberrant congenital bands is related to the difficulty of diagnosis, and cases of death with late detection have been documented. This research examines the expression of Caudal Type Homeobox 1 (CDX1), Indian Hedgehog (IHH), Sonic Hedgehog (SHH), GATA Binding Protein 4 (GATA4), Forkhead Box A2 (FOXA2) and Forkhead Box F1 (FOXF1) gene expression in human abdominal congenital adhesion fibroblast and endothelium cells by chromogenic in situ hybridization, with the aim of elucidating their potential association with the etiology of congenital intra-abdominal adhesion band development. The potential genes’ signals were examined using a semi-quantitative approach. Significant correlations were observed between the expression of CDX1 (p <.001) and SHH (p=0.032) genes in fibroblasts from congenital intra-abdominal adhesions compared to fibroblasts from control peritoneal tissue. Statistically significant very strong correlations were found between the CDX1 and IHH comparing endothelium and fibroblast cells in congenital abdominal adhesion bands. There was no statistically significant difference found in the distribution of IHH, FOXA2, GATA4, and FOXF1 between the fibroblasts and endothelium of the patients compared to the control group. The presence of notable distinctions and diverse associations suggests the potential involvement of numerous morpho-pathogenetic processes in the development of intraabdominal adhesions.
先天性腹腔粘连是一种罕见的疾病,可导致任何年龄段的小肠梗阻,在儿科人群中更为常见。病因至今不明,先天性异常腹腔粘连的重要性与诊断的难度有关,有文献记载发现过晚导致死亡的病例。这项研究检测了尾状同源染色体 1(CDX1)、印度刺猬(IHH)、声刺猬(SHH)、GATA 结合蛋白 4(GATA4)的表达、通过显色原位杂交研究人腹腔先天性粘连成纤维细胞和内皮细胞中叉头盒 A2(FOXA2)和叉头盒 F1(FOXF1)基因的表达,旨在阐明它们与先天性腹腔内粘连带发育病因的潜在联系。采用半定量方法对潜在基因的信号进行了检测。与对照腹膜组织的成纤维细胞相比,先天性腹腔内粘连的成纤维细胞中 CDX1(p <.001)和 SHH(p=0.032)基因的表达存在显著相关性。先天性腹腔粘连带内皮细胞和成纤维细胞的 CDX1 和 IHH 比较发现,两者之间存在统计学意义上的非常强的相关性。与对照组相比,患者的成纤维细胞和内皮细胞中 IHH、FOXA2、GATA4 和 FOXF1 的分布无明显统计学差异。明显的差异和多种关联的存在表明,腹腔内粘连的发生可能与多种形态-病理过程有关。
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引用次数: 0
Survival after Consecutive Myocardial Infarction and Stroke: A Case Report 连续心肌梗死和中风后的存活率:病例报告
Q3 Medicine Pub Date : 2024-05-22 DOI: 10.15388/amed.2024.31.1.14
Kristina Ratautė, Greta Burneikaitė, Jolita Badarienė
Background: Myocardial infarction and stroke are prevalent and potentially fatal urgent medical conditions. Stroke as a subsequent cardiovascular event after the myocardial infarction significantly decreases the odds of survival for the patient.Clinical case: We report a case of a 48-year-old man admitted to Vilnius University Hospital Santaros Klinikos due to an ST-segment elevation myocardial infarction. Patient also experienced a cardioembolic cerebral infarction on the tenth day in the hospital. The patient survived this dual infarction, his general condition improved and he was discharged to the rehabilitation center.Discussion and Conclusions: Cardiovascular diseases are the most common cause of death in the world. Stroke, as a complication of myocardial infarction, affects 0.76–3.2% of patients and demonstrates an increasing incidence trend. In such a dual infarction, in-hospital mortality can be as high as 18–41%. It is hopeful that targeted research and evidence-based prevention with treatment can improve outcomes of concomitant myocardial infarction and stroke.
背景:心肌梗死和脑卒中是普遍存在且可能致命的紧急医疗状况。中风作为心肌梗死后的继发性心血管事件,会大大降低患者的生存几率:我们报告了一例因 ST 段抬高型心肌梗死入住维尔纽斯大学 Santaros Klinikos 医院的 48 岁男性患者。住院第十天,患者还发生了心肌栓塞性脑梗塞。患者在这次双重梗塞中幸存下来,全身状况有所改善,出院后被送往康复中心:心血管疾病是世界上最常见的死亡原因。中风作为心肌梗死的并发症,影响着 0.76%-3.2% 的患者,且发病率呈上升趋势。在这种双重梗死中,院内死亡率可高达 18-41%。希望有针对性的研究和循证预防与治疗能改善并发心肌梗死和中风的预后。
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引用次数: 0
Double Parathyroid Adenoma Presenting as One Mass: A Case Report 双甲状旁腺腺瘤表现为一个肿块:病例报告
Q3 Medicine Pub Date : 2024-05-22 DOI: 10.15388/amed.2024.31.1.20
Rugilė Petruokaitė, V. Eismontas, N. Samalavičius
Background and Objectives: Primary hyperparathyroidism is a common endocrinological condition, which is usually caused by solitary parathyroid adenoma. The aim of this article is to present a case of double adenoma presenting as one and literature review on this topic.Case presentation: 56 years old female suffering from generalized fatigue, bone pain, unstable body weight and palpitations was diagnosed with primary hyperparathyroidism. Further investigation revealed elevated parathyroid hormone (PTH), ionized and total calcium levels. Imaging showed two adenomas merging into one. Parathyroidectomy was performed and final intraoperative PTH (IOPTH) decreased by 71.6%. Parathyroid adenoma measuring 40 mm x 15 mm x 11 mm and weighing 1 g 483 mg was excised. 7 weeks after surgery patient was feeling well but her PTH level was elevated again.Conclusions: As far as we know, the double parathyroid adenoma presented in this case report is the largest reported in the Northern Europe and the first one that presents as one mass within the region. Double adenoma increases the risk of recurrent primary hyperparathyroidism (PHPT) and requires more careful and longer follow up after surgery than solitary adenomas. Final IOPTH must decrease by at least 50% within 10 minutes. This case shows that despite final IOPTH drop by more than 50%, after few weeks normocalcemic elevated parathyroid hormone (NCePTH) phenomenon was noticed. This phenomenon does not indicate surgical failure.
背景和目的:原发性甲状旁腺功能亢进症是一种常见的内分泌疾病,通常由单发甲状旁腺腺瘤引起。本文旨在介绍一例双腺瘤并存的病例以及相关文献综述:56岁女性,全身乏力、骨痛、体重不稳定、心悸,被诊断为原发性甲状旁腺功能亢进。进一步检查发现甲状旁腺激素(PTH)、离子钙和总钙水平升高。影像学检查显示两个腺瘤合二为一。患者接受了甲状旁腺切除术,术中PTH(IOPTH)最终下降了71.6%。切除的甲状旁腺腺瘤大小为40 mm x 15 mm x 11 mm,重量为1 g 483 mg。术后7周,患者感觉良好,但PTH水平再次升高:据我们所知,本病例报告中的双甲状旁腺腺瘤是北欧地区报告的最大的腺瘤,也是该地区首个以单个肿块形式出现的腺瘤。双腺瘤会增加原发性甲状旁腺功能亢进症(PHPT)复发的风险,与单发腺瘤相比,术后需要更仔细、更长时间的随访。最终的 IOPTH 必须在 10 分钟内至少下降 50%。本病例显示,尽管最终IOPTH下降了50%以上,但几周后仍发现了正常钙化性甲状旁腺激素升高(NCePTH)现象。这种现象并不表示手术失败。
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引用次数: 0
Imaging and MR Spectroscopy in Papillary Craniopharyngioma 乳头状颅咽管瘤的成像和磁共振波谱分析
Q3 Medicine Pub Date : 2024-05-22 DOI: 10.15388/amed.2024.31.1.10
Ashima Mahajan, Bheru Dan Charan, Sushant Agarwal, Vinay Goel, Leve Joseph Devarajan Sebastian, Vaishali Suri, Ashish Suri, Ajay Garg
Sellar-suprasellar masses exhibit a diverse range of differential diagnoses and it is feasible to establish a preliminary diagnosis before surgery by evaluating conventional CT scans and contrast-enhanced MRI results. Nevertheless, certain cases may present with inconclusive findings, making it challenging to anticipate the underlying tissue composition accurately through imaging alone. Researchers have explored the application of Proton MR spectroscopy in analyzing suprasellar tumors, and their investigations have revealed that it can complement traditional MRI by enhancing the accuracy of preoperative diagnoses. In this context, we report three biopsy-proven cases of suprasellar papillary craniopharyngioma where the MRS spectra derived from the solid component exhibited noticeable lipid peaks alongside reduced levels of choline and NAA. These findings played a pivotal role in facilitating the correct preoperative identification of papillary craniopharyngioma.
ellar-suprasellar肿块的鉴别诊断多种多样,在手术前通过评估常规CT扫描和对比增强磁共振成像结果来确定初步诊断是可行的。然而,某些病例可能会出现不确定的结果,因此仅通过成像来准确预测潜在的组织成分具有挑战性。研究人员探索了质子磁共振波谱在分析鞍上肿瘤中的应用,他们的研究表明,质子磁共振波谱可以补充传统磁共振成像,提高术前诊断的准确性。在这种情况下,我们报告了三例经活检证实的鞍上乳头状颅咽管瘤病例,这些病例中固体成分的 MRS 图谱显示出明显的脂质峰,同时胆碱和 NAA 的水平也有所降低。这些发现在促进术前正确识别乳头状颅咽管瘤方面发挥了关键作用。
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引用次数: 0
Beyond Benign: A Case of Subependymal Giant Cell Astrocytomas Provoking Hydrocephalus in Tuberous Sclerosis Complex 超越良性:一例结节性硬化症复合体腮腺下巨细胞星形细胞瘤引发脑积水的病例
Q3 Medicine Pub Date : 2024-05-22 DOI: 10.15388/amed.2024.31.1.9
A. Navarro-Ballester, Rosa Álvaro-Ballester, Miguel Ángel Lara-Martínez
22-year-old male diagnosed with Tuberous Sclerosis Complex (TSC), a genetic disorder characterized by benign tumors in various organs, with a focus on neurological implications. Central to the study is the development of Subependymal Giant Cell Astrocytomas (SEGAs), leading to hydrocephalus in the patient. The diagnosis of TSC was made in the patient’s childhood, and he was monitored regularly. The study highlights a significant growth in a subependymal nodule, leading to monoventricular hydrocephalus. MRI scans played a crucial role in identifying the progression of SEGAs and the subsequent hydrocephalus. The treatment approach involved endoscopic surgical removal of the SEGA, with histopathology confirming the diagnosis. Post-surgical outcomes over an eight-year follow-up period showed a normalization in ventricular size and the stability of other subependymal nodules, without any complications. This case underscores the importance of regular monitoring for TSC patients, early intervention for complications like hydrocephalus, and the need for a multidisciplinary treatment approach. The case study provides valuable insights into the management of neurodevelopmental disorders and the complexities surrounding TSC and SEGAs.
22 岁的男性被诊断患有结节性硬化综合症(TSC),这是一种遗传性疾病,其特征是在不同器官中长出良性肿瘤,重点是对神经系统的影响。这项研究的核心内容是腮腺下巨细胞星形细胞瘤(SEGAs)的发展,导致患者出现脑积水。TSC的诊断是在患者童年时做出的,并对他进行了定期监测。研究显示,蝶鞍下结节明显增大,导致单房性脑积水。核磁共振成像扫描在确定SEGAs的进展和随后的脑积水方面发挥了至关重要的作用。治疗方法是通过内窥镜手术切除SEGA,并通过组织病理学确诊。手术后八年的随访结果显示,脑室大小恢复正常,其他蝶鞍下结节也趋于稳定,没有出现任何并发症。该病例强调了对 TSC 患者进行定期监测、对脑积水等并发症进行早期干预的重要性,以及采用多学科治疗方法的必要性。本病例研究为神经发育性疾病的治疗以及围绕TSC和SEGAs的复杂性提供了宝贵的见解。
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引用次数: 0
Determinants of Parental Attitudes towards Children’s Vaccination in Lithuania: An Online Survey 立陶宛家长对儿童接种疫苗态度的决定因素:在线调查
Q3 Medicine Pub Date : 2024-05-07 DOI: 10.15388/amed.2024.31.1.7
Kamilė Čeponytė, Eglė Narkevičiūtė, Aušra Beržanskytė, Sigita Burokiene
Background: Data from recent years show that the COVID-19 pandemic has significantly reduced the scope of child immunisation worldwide. If the numbers continue to fall, we may have a vaccination crisis. In order to understand the local factors of this phenomenon, we studied parents‘ viewpoint towards childhood vaccination in Lithuania. Therefore, the aim of our study was to determine the impact of parental attitudes on children’s vaccination.Materials and Methods: A web-based cross-sectional study was made in Lithuania from October 20th to November 3rd, 2020, using Google Forms. An anonymous questionnaire included both quantitative and qualitative questions. The questionnaire was distributed to the general population in Lithuania via social media and a snowball sampling. Only parents who have at least one child under 18 years old were involved in the study. We analysed the parents’ attitudes towards vaccination by their socioeconomic and demographic determinants using MS Excel and OpenEpi tools. The respondents were considered vaccine supporters if they vaccinated all their children with state-reimbursed vaccines or only vaccinated some of their children, and vaccine sceptics if they did not vaccinate their children with state-reimbursed vaccines.Results: The population of our research consisted of 775 parents. There were more males against vaccination than females, respectively, 59.6% and 33.2%. 65.0% of all respondents stated that they vaccinated their children with the full course of vaccines, while the remaining 35.0% did not vaccinate. University-level education dominated in both pro-vaccine and anti-vaccine groups. We found that 16.9% of parents who were unvaccinated as children themselves tend not to vaccinate their children. However, in the pro-vaxx group, only 0.7% of parents were unvaccinated during childhood. 50.8% of vaccine sceptics were not fully informed by healthcare professionals about the benefits and risks of vaccination, while only 31.6% of vaccine supporters were not informed. Social environment did not have an impact on the decision whether to vaccinate or not to vaccinate a child among both vaccine advocates and vaccine deniers (accordingly, 51.2% and 42.9%). 29.3% of respondents stated that the cost of paid vaccinations was too high. Open-text survey responses gave us more in-depth insight about the parental decision-making process. Protection of children and society from infectious diseases (31.7%) was mentioned as the main reason for vaccination. Whereas vaccine-hesitant parents were mostly concerned about already-occurring side effects or their risk (43.4%).Conclusions: Our findings confirmed that vaccine hesitancy was associated with not being vaccinated in childhood themselves, lack of information from medical practitioners and male gender. The price of vaccines also had an impact on immunisation rates – more than one-third of the vaccine supporting parents indicated that the cost of paid vaccinations was too high. Th
背景:近年来的数据显示,COVID-19 大流行大大缩小了全球儿童免疫接种的范围。如果数量继续下降,我们可能会面临疫苗接种危机。为了了解造成这一现象的当地因素,我们研究了立陶宛家长对儿童疫苗接种的看法。因此,我们的研究旨在确定家长的态度对儿童接种疫苗的影响:2020 年 10 月 20 日至 11 月 3 日,我们使用谷歌表格在立陶宛开展了一项基于网络的横断面研究。匿名问卷包括定量和定性问题。问卷通过社交媒体和滚雪球式抽样向立陶宛的普通民众发放。只有至少有一名 18 岁以下子女的父母参与了研究。我们使用 MS Excel 和 OpenEpi 工具,根据家长的社会经济和人口统计决定因素分析了他们对疫苗接种的态度。如果受访者为其所有子女接种了国家报销的疫苗或仅为部分子女接种了疫苗,则被视为疫苗支持者;如果受访者未为其子女接种国家报销的疫苗,则被视为疫苗怀疑者:我们的研究对象包括 775 名家长。反对接种疫苗的男性多于女性,分别为 59.6% 和 33.2%。65.0%的受访者表示他们为孩子接种了全套疫苗,其余 35.0%的受访者没有接种疫苗。在支持接种疫苗和反对接种疫苗的群体中,受过大学教育的人都占多数。我们发现,16.9% 的父母在自己的孩子小时候没有接种过疫苗,他们倾向于不给孩子接种疫苗。然而,在支持接种疫苗组中,只有 0.7% 的家长在儿童时期未接种过疫苗。50.8%的疫苗怀疑者没有从医疗保健专业人员那里充分了解接种疫苗的益处和风险,而只有 31.6% 的疫苗支持者没有了解相关信息。在疫苗支持者和疫苗否定者中,社会环境对决定是否给孩子接种疫苗没有影响(分别为 51.2% 和 42.9%)。29.3%的受访者表示付费疫苗接种的费用太高。开放文本的调查回答让我们对家长的决策过程有了更深入的了解。保护儿童和社会免受传染病侵害(31.7%)被认为是接种疫苗的主要原因。而对疫苗犹豫不决的家长则主要担心已经出现的副作用或其风险(43.4%):我们的研究结果证实,疫苗接种犹豫与儿童时期未接种疫苗、缺乏医生提供的信息以及男性性别有关。疫苗的价格对免疫接种率也有影响--三分之一以上支持接种疫苗的家长表示,付费接种疫苗的费用太高。鼓励家长接种疫苗的主要原因是他们希望保护自己的孩子和社会免受传染病的侵害。而不愿意接种疫苗的家长则主要担心已经出现的副作用或风险。对于在立陶宛是否应强制儿童接种疫苗的问题没有达成共识,因为对这一问题的回答几乎是平均分布的。家长对儿童疫苗接种态度的形成是一个复杂的过程,取决于家长对医疗保健系统的态度、对医生缺乏信任以及在疫苗接种的益处和风险方面的沟通不足。在制定卫生政策时应考虑到所有这些信息。
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引用次数: 0
Deaths during Sexual Activity 性活动中的死亡
Q3 Medicine Pub Date : 2024-05-07 DOI: 10.15388/amed.2024.31.1.8
Agnė Okulevičiūtė, Sigitas Chmieliauskas, Sigitas Laima, Diana Vasiljevaitė, Jurgita Stasiūnienė
Background: Deaths during sexual activities are a rarely identified phenomenon in forensic medicine practice. Most often, such deaths are classified as accidents or deaths due to the manifestation of certain diseases during sexual activity. It is important to rule out homicide or suicide as the cause of death when investigating sexual deaths. Determining the cause of death requires a comprehensive assessment of the evidence and circumstances and should not be based solely on autopsy findings. When determining the cause of death, it is necessary to evaluate the circumstances of the discovery, important evidence found near the body, the position of the deceased, the place where the deceased was found, and the characteristics of the environment.Cases: Case 1: A 65-year-old male was clothed in women’s underwear and was found hanging in a noose in a bedroom after a house fire. The autopsy revealed a ligature mark on the neck, bruises in neck muscles, tears in carotid arteries, and signs of acute pulmonary distension. The cause of death was determined to be suffocation due to neck compression by a ligature, compounded by significant alcohol intoxication, with additional postmortem burns covering 30% of the body surface area likely occurring after death.Case 2: A 55-year-old naked male was found without external injuries but with a plastic tube inserted into the rectum, causing a 2.5 cm rupture in the ileum. The perforation led to complications, including purulent diffuse peritonitis, intoxication, and acute cardiac and respiratory failure, resulting in death within 3-6 hours after insertion. Concurrent findings included atherosclerotic changes in the heart, internal organ hyperemia and edema, hepatic steatosis, renal cyst, and a lack of ethyl alcohol in blood but 0.17 ‰ presence in urine according to toxicology analysis.Conclusions: A detailed evaluation of all the evidence is very important in the forensic examination of the deceased during sexual activity. Therefore, to determine the cause of death, not only the autopsy data, toxicological and microscopic examinations of the deceased are important, but also the evaluation of all findings at the scene. The most common cause of death of an autoerotic nature is asphyxia, and the most commonly identified group of the dead are men aged around 40 years.
背景:在法医学实践中,性活动中的死亡是一种很少被发现的现象。大多数情况下,这类死亡被归类为意外事故或在性活动中因某些疾病表现而导致的死亡。在调查性死亡时,必须排除他杀或自杀的死因。确定死因需要对证据和情况进行全面评估,而不应仅仅依据尸检结果。在确定死因时,有必要对发现时的情况、尸体附近发现的重要证据、死者的位置、发现死者的地点以及环境特征进行评估:案例 1:一名 65 岁的男性身着女性内衣,被发现用绳套吊死在房屋火灾后的卧室里。尸检显示颈部有勒痕,颈部肌肉有瘀伤,颈动脉撕裂,并有急性肺胀的迹象。病例 2:一名 55 岁的裸体男性被发现时没有外伤,但有一根塑料管插入直肠,造成回肠 2.5 厘米的破裂。穿孔导致并发症,包括化脓性弥漫性腹膜炎、中毒、急性心力衰竭和呼吸衰竭,导致患者在插管后 3-6 小时内死亡。并发症包括心脏动脉粥样硬化病变、内脏器官充血和水肿、肝脏脂肪变性、肾囊肿,根据毒理学分析,血液中没有乙醇,但尿液中含有 0.17 ‰的乙醇:对所有证据进行详细评估在对性活动中的死者进行法医检查时非常重要。因此,要确定死因,不仅死者的尸检数据、毒理学检查和显微镜检查很重要,对现场所有发现的评估也很重要。最常见的自身性行为死亡原因是窒息,最常见的死者群体是 40 岁左右的男性。
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引用次数: 0
Wunderlich Syndrome Managed with Angiomyolipoma Embolization – Renal Artery Anatomic Variant Augmenting Safe and Nephron-Sparing Intervention 用血管肌脂肪瘤栓塞术治疗 Wunderlich 综合征--肾动脉解剖变异增强了安全的保肾干预措施
Q3 Medicine Pub Date : 2024-03-05 DOI: 10.15388/amed.2024.31.1.3
Tara Prasad Tripathy, Alamelu Alagappan, R. Patel, Srikant Kumar Behera, Sandip Kumar Panda, Suprava Naik
Background: Wunderlich syndrome is an uncommon entity characterized by spontaneous, nontraumatic renal bleeding into the subcapsular and perirenal regions. The most frequent benign tumor, angiomyolipoma, is the most common cause of Wunderlich syndrome.Case presentation: We report a case of Wunderlich syndrome in angiomyolipoma. Intratumoral pseudoaneurysm arising from feeders of an accessory renal artery supplying the lower pole of the kidney was selectively embolized. Rarely does a sporadic renal angiomyolipoma develop a giant pseudoaneurysm.Conclusion: Transarterial embolization is imperative to control the bleeding or as a preventative measure to reduce the risk of intralesional pseudoaneurysm rupture. When vascular interventional facilities are unavailable, surgery may be necessary.
背景:Wunderlich综合征是一种不常见的疾病,其特点是自发性、非外伤性肾出血,出血部位位于肾囊下和肾周。最常见的良性肿瘤--血管肌脂肪瘤是导致 Wunderlich 综合征的最常见原因:我们报告了一例血管肌脂肪瘤 Wunderlich 综合征病例。我们选择性地栓塞了由供应肾脏下极的附属肾动脉供血源引起的瘤内假性动脉瘤。结语:经动脉栓塞治疗肾血管瘤是非常重要的:结论:经动脉栓塞治疗对于控制出血或作为预防措施降低区域内假动脉瘤破裂的风险至关重要。如果没有血管介入设备,则可能需要手术治疗。
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引用次数: 0
Hematohidrosis in Pediatric Practice  – a Case Report and Review of the Literature 儿科血汗症--病例报告和文献综述
Q3 Medicine Pub Date : 2024-02-29 DOI: 10.15388/amed.2024.31.1.2
Oksana Matsyura, Lesya Besh, Svitlana Jefimova, Kh.B. Slivinska-Kurchak, Sergiy Gerasymov
Hematohidrosis (bloody sweat) is a symptom of trophic damage to the vascular wall, in which sweat mixes with blood and seeps onto undamaged areas of the skin in the form of red or pink liquid (depending on the ratio of sweat to blood).  In our study we have analyzed 25 case reports of hematohidrosis in children, reported throughout the world using PubMed, ResearchGate with detailed description and opened access. We took into consideration: age of the patient, sex, location of bloody excretion, cause or trigger, treatment and its effectiveness.Our clinical case present a 9-year-old girl complained of a periodic bleeding from the intact skin of the face, neck, thighs (without visible damage to the skin) manifested by red or pink liquid, nosebleeds, and bloody discharge from the mucous membrane of the eyes. The secretions were of varying intensity and lasted up to several hours. Most of all episodes are associated with a strong emotional exertion. One of the theories of hematohidrosis pathogenesis is evident vasoconstriction of the blood vessels surrounding the sweat glands, provoked by hyperactivation of the sympathetic nervous system, which is followed by their excessive vasodilation up to rupture and blood entering the sweat gland ducts. Capillary endothelial cells are known to contain β2-adrenoceptors, which, through the modulation of nitric oxide release, cause endothelium-dependent vasodilation. Blocking β-adrenoceptors (for example, propranolol) prevents excessive vasodilation of blood vessels and, accordingly, their rupture and blood flow to the sweat gland.We managed to find out that the patient’s bloody sweat was a manifestation of a separate pathological phenomenon, and not one of the symptoms of another disease. A properly formed treatment complex and the great trust of the parents enabled to stabilize the child’s condition, and later to cure her. Currently, hematohidrosis is recognized as an independent disease that requires in-depth study of the triggering mechanisms of development, pathogenetic and clinical features.
血汗症(血汗)是血管壁营养性损伤的一种症状,在这种情况下,汗液与血液混合,以红色或粉红色液体(取决于汗液与血液的比例)的形式渗入皮肤未受损部位。 在我们的研究中,我们利用 PubMed、ResearchGate 等网站分析了世界各地报道的 25 例儿童血汗症病例,并进行了详细描述和开放访问。我们的临床病例是一名 9 岁女孩,主诉面部、颈部、大腿完整皮肤周期性出血(皮肤无明显损伤),表现为红色或粉红色液体、流鼻血和眼睛粘膜血性分泌物。分泌物强度不一,持续时间长达数小时。所有发作大多与强烈的情绪激动有关。血汗病的发病机理之一是交感神经系统过度激活引起汗腺周围血管明显收缩,随后血管过度扩张直至破裂,血液进入汗腺导管。已知毛细血管内皮细胞含有 β2-肾上腺素受体,它通过调节一氧化氮的释放,导致内皮依赖性血管扩张。阻断 β2-肾上腺素受体(如普萘洛尔)可防止血管过度扩张,从而防止血管破裂和血液流向汗腺。适当的综合治疗和家长的高度信任使患儿的病情得以稳定,随后又治愈了她。目前,血汗症被认为是一种独立的疾病,需要深入研究其发病诱因、发病机制和临床特征。
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引用次数: 0
Bilateral Renal Hilar Nutcracker Phenomenon in a Male Cadaver 一具男性尸体的双侧肾门胡桃钳现象
Q3 Medicine Pub Date : 2024-02-28 DOI: 10.15388/amed.2024.31.1.6
D. Borthakur, Rajesh Kumar, V. Dhawan, Rima Dada
Nutcracker phenomenon (NCP) typically refers to the entrapment of the left renal vein (LRV) between the aorta and the superior mesenteric artery. Similar to the classic NCP, the renal vein can also get entrapped between the segmental branches of the renal artery at the renal hilum, which has been referred to as ‘renal hilar nutcracker phenomenon (RHNP).’ During routine dissection of a male cadaver of 67 years, the renal veins of both sides at the renal hilum were seen between the segmental branches of renal arteries, which we identified as the ‘renal hilar nutcracker phenomenon.’ The disposition of the rest of the perihilar structures was normal. ‘Renal hilar nutcracker phenomenon’ can have similar clinical presentation like that of the nutcracker phenomenon. Hence, knowledge of such anatomical variation at the renal hilum is desirable.
胡桃钳现象(NCP)通常是指左肾静脉(LRV)被夹在主动脉和肠系膜上动脉之间。与典型的 NCP 类似,肾静脉也可能被夹在肾动脉在肾门的节段分支之间,这被称为 "肾门胡桃钳现象(RHNP)"。在对一具 67 岁的男性尸体进行常规解剖时,我们在肾动脉节段分支之间看到了肾门处两侧的肾静脉,我们将这种现象称为'肾门胡桃钳现象'。肾周其他结构的布局正常。肾门胡桃钳现象 "的临床表现与胡桃钳现象相似。因此,了解肾门的这种解剖变异是很有必要的。
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Acta Medica Lituanica
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