postmortem examination

验尸
  • 文章类型: Journal Article
    由闪电引起的死亡事故分为观察事件和未观察事件。在外部验尸过程中,通常会忽略病因学或特征性发现。可能会出现典型的错误,这通常会导致错误的诊断。对美国经济区e.V.(ABBW)的闪电导体建设委员会的历史收藏进行了270人死亡的分析,涉及1951-1965年期间在德国发生的闪电致命事故。此外,进行了选择性的文献研究。这项研究的目的是分析死亡现场,衣服,还有受害者.作者集中研究了与正确诊断“闪电死亡”相关的主要发现。“Lichtenberg人物和烧焦的体毛都被认为是雷击的代名词。问题是利希滕贝格是否有数字,例如,代表了最经常导致正确诊断的发现。在案件收集的270名闪电受害者中,129(47.8%)的头发被烧焦,25(9.3%)的头发被Lichtenberg数字。两个报告发现的频率的比较,烧焦的体毛与利希滕贝格的人物,仅在文献中对病例数低于40的病例进行了研究。这项研究是对闪电造成的大量致命事故的首次评估。据报道,与Lichtenberg的数字相比,雷击受害者中的尸体毛发更加频繁。这项研究表明,烧焦的体毛可能比Lichtenberg的数字在诊断上更重要。
    Lethal accidents caused by lightning are divided into observed and unobserved events. Pathognomonic or characteristic findings are often overlooked during external postmortem examination. Classical mistakes may be made which may often lead to an incorrect diagnosis. An analysis of 270 fatalities was performed on a historical collection of the Committee for Lightning Conductor Construction for the United Economic Area e. V. (ABBW) on lethal accidents due to lightning that occurred in Germany for the period 1951-1965. Furthermore, a selective literature research was carried out. The aim of the study was to analyze the death scene, the clothing, and the victim. The authors focused on chief findings which were relevant to the correct diagnosis of \"death by lightning.\" Both Lichtenberg figures and singed body hair were considered pathognomonic for a lightning strike. The question arose as to whether Lichtenberg figures, for example, represented the finding that most often led to the correct diagnosis. Of the 270 lightning-struck victims from the case collection, 129 (47.8%) had singed body hair and 25 (9.3%) had Lichtenberg figures. A comparison of the frequency of the two reported findings, singed body hair versus Lichtenberg figures, has only been performed in the literature for case numbers below 40. This study is the first evaluation of a relatively large number of lethal accidents due to lightning. Singed body hair was reported more frequently in lightning-struck victims than Lichtenberg figures. This study showed that singed body hair is probably more diagnostically important than Lichtenberg figures.
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  • The coronavirus disease 2019 (COVID-19) has been a global epidemic for more than three years, causing more than 6.9 million deaths. COVID-19 has the clinical characteristics of strong infectivity and long incubation period, and can cause multi-system damage, mainly lung damage, clinical symptoms of acute respiratory distress syndrome (ARDS) and systemic multiple organ damage. The SARS-CoV-2 virus is still constantly mutating. At present, there is no global consensus on the pathological changes of COVID-19 associated deaths and even no consensus on the criteria for determining the cause of death. The investigation of the basic pathological changes and progression of the disease is helpful to guide the clinical treatment and the development of therapeutic drugs. This paper reviews the autopsy reports and related literature published worldwide from February 2020 to June 2023, with a clear number of autopsy cases and corresponding pathological changes of vital organs as the inclusion criteria. A total of 1 111 autopsy cases from 65 papers in 18 countries are included. Pathological manifestations and causes of death are classified and statistically analyzed, common pathological changes of COVID-19 are summarized, and analytical conclusions are drawn, suggesting that COVID-19 infection can cause life-threatening pathological changes in vital organs. On the basis of different health levels of infected groups, the direct cause of death is mainly severe lung damage and secondary systemic multiple organ failure.
    新型冠状病毒感染(coronavirus disease 2019,COVID-19)已在全球流行超过3年,造成690多万人死亡。COVID-19具有强传染性和长潜伏期的临床特点,能造成以肺损伤为主的多系统损伤,临床出现急性呼吸窘迫综合征以及全身多器官损伤症状,其病毒SARS-CoV-2仍在不断变异。目前全球对COVID-19相关死亡的病理改变乃至于死因判断标准并未达成共识,调查该疾病的基本病变和病变进展,有助于指导临床治疗以及治疗药物的研制。本文综述了全球2020年2月至2023年6月发表的COVID-19尸体检验报告及相关文献,以有明确的尸体检验案例数量以及对应的重要器官病理学改变为纳入标准,共纳入来自18个国家65篇论文的1 111例尸体检验案例,对病理表现和死因进行归类和统计学分析,归纳和总结了COVID-19的共性病理变化,并提出分析结论,认为COVID-19感染能引起全身重要器官发生危及生命的病理改变,在感染群体健康水平各异的基础上,死亡案例的直接死因主要为严重的肺部损伤及其继发的全身多器官功能衰竭。.
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  • 文章类型: Journal Article
    OBJECTIVE: To explore the characteristics of postmortem examination, chemical examination and scene investigation of deaths caused by oral diphenidol hydrochloride poisoning, and so as to provide a reference for proper settlement and prevention of such deaths.
    METHODS: The data of 22 deaths caused by oral diphenidol hydrochloride poisoning in a city from January 2018 to August 2020 were collected, including case details, scene investigations, autopsies, chemical examinations and digital evidence. Thirty-one cases of deaths caused by oral diphenidol hydrochloride poisoning reported in previous literature were also collected.
    RESULTS: In the 53 oral diphenidol hydrochloride poisoning death cases, 50 cases were suicide, 2 cases were accidental, while 1 case was undetermined. Fifty-two cases were found in the medical records or crime scene investigation reports with doses ranging from 775 mg to 12 500 mg, and 23 deceased were detected with postmortem blood concentrations ranging from 2.71 mg/L to 83.1 mg/L. Clinical symptoms were recorded in 6 patients, including conscious disturbance and convulsion. Among the 45 cases which were performed with external examination, 23 cases autopsied.
    CONCLUSIONS: Most of the deceased of oral diphenidol hydrochloride poisoning were suicide. No significant correlation was found between dose and blood concentration through the retrospective analysis of cases.
    目的: 探讨口服盐酸地芬尼多中毒死亡案例的尸体检验、理化检验和现场勘验特点,为相关案(事)件的处置和预防提供参考。方法: 收集某市2018年1月—2020年8月发生的22例口服盐酸地芬尼多中毒死亡案例的案情、现场勘验、尸体检验、理化检验、电子物证等资料,结合既往文献报道的31例口服盐酸地芬尼多中毒死亡案例进行分析。结果: 53例口服盐酸地芬尼多中毒死亡案例中,50例为自杀,2例为意外,1例性质不详。52例在病历记录或现场勘验记录中找到服药剂量,范围为775~12 500 mg。有服药剂量的52例中,23例经死后药物浓度检测,血药质量浓度范围为2.71~83.1 mg/L。记录有临床症状的6例,表现为意识障碍、抽搐。经尸表检查的45例中,有23例进行了尸体解剖。结论: 口服盐酸地芬尼多中毒死者多数为自杀。通过多个案例的回顾性分析,尚未发现服药剂量与血药浓度之间具有相关性。.
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  • 文章类型: Journal Article
    大多数人更喜欢在家中提供临终关怀。尽管日本试图推广家庭护理和临终关怀,在日本,很少有人死在家里。另一方面,在家中死亡不一定是通过临终关怀在家中死亡,因为它们包括许多死亡,例如外部原因死亡和单独死亡。我们获得了大阪市主要地区家中验尸次数的数据,并通过从家中总死亡人数中减去家中验尸次数,计算出估计的家中有人死亡人数。我们从法医学角度分析了医疗资源对临终关怀的贡献,以更深入地分析实际情况。方法采用人口数据,总死亡人数,在家里死亡,与大阪市家庭护理相关的医疗资源是从日本一家公共机构的网站获得的。有关大阪市验尸次数的数据是从大阪医学检查官办公室获得的。估计家中有人死的人数是通过从家中的总死亡人数中减去家中的验尸来计算的。我们对医疗资源的数量和在家参加死亡的患病率进行了单变量和多变量分析。结果在单因素分析中,家庭随诊死亡的患病率,在“医生”中观察到高度正相关,“总诊所,除HCSC外的诊所,“和”普通床。在长期护理床中观察到高度负相关。“在多变量分析中,除HCSC外,在诊所观察到一个正系数,在HCSC或HCSH中观察到阴性。“结论将普通诊所和医院改为HCSC和HCSH的政策可能对终末期护理无效,因为标准不包括对床位数量或使用的任何限制。然而,普通诊所可能在临终关怀中发挥了重要作用,即使他们不是HCSC。
    Introduction Most people would prefer end-of-life care to be provided at home. Although Japan has tried to promote home care and end-of-life care, very few people die at home in Japan. On the other hand, deaths at home are not necessarily attended deaths at home by end-of-life care because they include many deaths, such as deaths from external causes and solitary deaths. We obtained the data on the number of postmortem examinations at home in the main areas of Osaka City and calculated the estimated number of attended deaths at home by subtracting the number of postmortem examinations at home from the number of total deaths at home. We analyzed the contribution of medical resources to end-of-life care from a forensic perspective for a closer analysis of the actual situation. Methods The data about the population, the number of total deaths, deaths at home, and medical resources related to home care in Osaka City was obtained from the website of a public institution in Japan. The data about the number of postmortem examinations in Osaka City was obtained from the Osaka Medical Examiner\'s Office. The estimated number of attended deaths at home was calculated by subtracting postmortem examinations at home from total deaths at home. We conducted univariate and multivariate analyses between the number of medical resources and the prevalence of attended deaths at home. Results In the univariate analysis of the prevalence of attended deaths at home, a high positive correlation was observed in \"doctors,\" \"total clinics,\" \"clinics except HCSC,\" and \"general beds.\" A high negative correlation was observed in \"long-term care beds.\" In the multivariate analysis, a positive coefficient was observed in \"clinics except HCSC,\" and a negative one was observed in \"HCSC or HCSH.\" Conclusion The policy of shifting general clinics and hospitals to HCSC and HCSH may not be as effective for end-of-life care because the criteria do not include any restrictions on the number or use of beds. However, general clinics may have played an important role in end-of-life care, even if they were not HCSC.
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  • 文章类型: Case Reports
    弥漫性大B细胞淋巴瘤是最常见的淋巴瘤,占所有非霍奇金淋巴瘤的30%;它们可以迅速生长,通常以肿块浸润组织或阻塞器官的形式出现。我们报告了一名58岁的女性,她有一个月的全身无力和体重减轻的病史,有两周的眼睛发黄的病史,发烧,呼吸困难,和双侧腿部肿胀。演示时的检查显示苍白,发烧,黄疸,肝肿大,双侧凹陷性踏板水肿。实验室检查显示严重贫血,混乱的凝血特征,氮质血症,肝酶升高,和升高的肿瘤标志物CA125,CEA,和CA19.9。腹部超声显示肝肿大和胰头大。最初的诊断是由于胰头癌引起的阻塞性黄疸。尽管提供了所有的照顾,她的临床病情恶化,直到入院第12天死亡。尸检显示胰头和胆管有肿块,主动脉旁和肠系膜淋巴结肿大伴腹水,心包结节,还有支气管肺炎.死后活检的组织学和免疫组织化学分析证实了弥漫性大B细胞淋巴瘤的诊断。该病例突出了在播散性弥漫性大B细胞淋巴瘤中经常出现的诊断困境。患者具有与不同器官和系统相关的特征。如果早期发现,大多数病例对标准免疫化疗有反应。然而,它也会迅速致命并最终导致死亡,正如在这个案例中看到的。
    Diffuse large B-cell lymphoma is the most common lymphoma, accounting for 30% of all non-Hodgkin lymphomas; they can grow rapidly and often present as masses infiltrating tissues or obstructing organs. We report the case of a 58-year-old female who presented with a one-month history of generalized body weakness and weight loss with a two-week history of yellowness of the eyes, fever, dyspnea, and bilateral leg swelling. Examination at presentation revealed pallor, fever, jaundice, hepatomegaly, and bilateral pitting pedal edema. Laboratory investigations revealed severe anemia, deranged clotting profile, azotemia, elevated liver enzymes, and elevated tumor markers CA125, CEA, and CA 19.9. Abdominal ultrasound showed hepatomegaly and a large head of the pancreas. The initial diagnosis was obstructive jaundice due to carcinoma of the head of the pancreas. Despite all care offered, her clinical condition deteriorated until she died on the 12th day of admission. A postmortem examination showed a mass in the head of the pancreas and bile duct, enlarged para-aortic and mesenteric lymph nodes with ascites, pericardial nodules, and bronchopneumonia. Histological and immunohistochemical analysis of postmortem biopsies confirmed the diagnosis of a diffuse large B cell lymphoma.  This case highlights the diagnostic dilemma often seen in disseminated diffuse large B-cell lymphoma. The patient presented with features referable to different organs and systems. If detected early, most cases respond to standard immuno-chemotherapy. However, it can also become rapidly fatal and ultimately lead to death, as seen in this case.
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  • 文章类型: Multicenter Study
    目的:胎盘感染SARS-CoV2可导致胎盘功能不全和胎儿宫内死亡。目前尚不清楚SARS-CoV2的胎儿胎盘感染是胎儿死亡的原因。我们的目的是确认和量化SARS-CoV2作为胎儿死亡原因的可归性。
    方法:我们在1月1日(法国)巴黎地区31家妇产医院的三个胎儿病理单元进行了尸检,2020年1月1日,2022年。所有胎儿死亡和终止妊娠的病例都受益于这些单位的详细胎盘病理检查。在数据库中搜索了宫内胎儿死亡和终止妊娠的病例。排除胎儿畸形或细胞遗传学异常的病例,以避免偏倚。我们包括1)胎盘或“不确定”原因的宫内胎儿死亡2)在子宫内胎儿生长严重受限的情况下终止妊娠。每个胎盘被送到一个病毒学单元,由对最初的验尸报告不知情的同一实验室技术人员进行RT-PCR测试。我们的主要终点是这些纳入病例中胎盘SARS-CoV2-PCRs阳性的比例。
    结果:超过2年,在147,722次交付中,记录了788次子宫内胎儿死亡和在子宫内胎儿生长严重受限的情况下终止妊娠的尸检,其中462次(58.6%)。共有13/462(2.8%)胎盘检测出SARS-CoV2阳性。鉴定了野生型及其α和δ变体。所有阳性病例均有胎盘功能障碍的组织学病变。SARS-CoV2胎盘炎与胎盘上的慢性夹耳炎和/或大量纤维蛋白沉积之间存在很强的相关性。当两个病变都存在时,诊断胎盘SARS-CoV2感染的特异性和阴性预测值分别为0.99(CI95[0.98-1.00])和0.96(CI95[0.94-0.98]).
    结论:在SARS-CoV2大流行的高峰期,巴黎地区超过一半的胎儿死亡原因被标记为胎盘或基于尸检结果的不明来源,但是我们的研究表明,在这些原因中,2.8%是由于胎盘SARS-CoV2感染,具有特定的组织学参与模式。这项研究强调了在死产评估中进行SARS-CoV2筛查的必要性。疫苗接种覆盖率的影响尚待确定。本文受版权保护。保留所有权利。
    Placental infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) can lead to placental insufficiency and in-utero fetal death (IUFD). The objective of this study was to confirm and quantify the extent to which fetoplacental infection with SARS-CoV-2 is a cause of fetal death.
    This was a multicenter retrospective cohort study of fetal deaths that underwent postmortem examination between January 2020 and January 2022 in three fetal pathology units in Paris, France. All cases of IUFD and termination of pregnancy (TOP) occurring in 31 maternity hospitals in the Paris region undergo detailed placental pathological examination in these units. Databases were searched for cases of IUFD and TOP. Cases with fetal malformation or cytogenetic abnormality were excluded to avoid bias. We included cases of IUFD with a placental or undetermined cause and cases of TOP in the context of severe intrauterine growth restriction (IUGR). Placentas were sent to a single virology unit for reverse-transcription polymerase chain reaction (RT-PCR) testing by a single laboratory technician blinded to the initial postmortem examination report. Our primary endpoint was the proportion of positive placental SARS-CoV-2 RT-PCR tests in the cohort.
    Among 147 722 deliveries occurring over 2 years, 788 postmortem examinations for IUFD and TOP for severe IUGR were recorded, of which 462 (58.6%) were included. A total of 13/462 (2.8%) placentas tested positive for SARS-CoV-2 by RT-PCR. Wild-type virus and alpha and delta variants were identified. All positive cases had histological lesions consistent with placental dysfunction. There was a strong correlation between SARS-CoV-2 placentitis and the presence of chronic intervillositis and/or massive fibrin deposits in the placenta. When both lesion types were present, the specificity and negative predictive value for the diagnosis of placental SARS-CoV-2 infection were 0.99 (95% CI, 0.98-1.00) and 0.96 (95% CI, 0.94-0.98), respectively.
    At the height of the SARS-CoV-2 pandemic, the cause of more than half of fetal deaths in the Paris area was determined by postmortem analysis to be of placental or undetermined origin. Of these cases, 2.8% were due to placental SARS-CoV-2 infection with a specific pattern of histological involvement. This study highlights the need for SARS-CoV-2 screening in stillbirth assessment. The impact of vaccination coverage remains to be established. © 2023 The Authors. Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of International Society of Ultrasound in Obstetrics and Gynecology.
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  • 文章类型: Journal Article
    22q11.2缺失综合征(22q11.2DS)是最常见的微缺失综合征。由于其可变的临床表型,产前诊断可能具有挑战性。这项回顾性研究的目的是评估产前诊断为22q11.2缺失综合征(DS)的病例的临床过程和妊娠结局,以及评估产前磁共振成像(MRI)和尸检的作用。总的来说,包括2012年至2022年在维也纳医科大学妇产科接受产前超声检查和妊娠护理的21例患者。大多数病例是使用荧光原位杂交(FISH)进行遗传诊断的。遗传诊断时的中位胎龄(GA)为23.0周(IQR21.4-24.8周)。在所有胎儿中均检测到CHD,最常见的心外表现是胸腺发育不全/发育不全,其次是泌尿生殖系统异常。产前磁共振成像(MRI)在十例病例中有三例显示了其他诊断信息。总的来说,14名患者选择了药物诱导的TOP,其中9例在引产前进行了致产剂。大多数颅面畸形仅通过尸检发现。总之,产前诊断为22q11.2DS的大多数病例除了检测到CHD外,在产前还注意到胸腺缺失或发育不全,几乎一半的病例有另一个主要来自泌尿生殖系统的心外畸形。此外,产前MRI证实了先前发现的畸形,但只在十分之三的病例中提供了额外的诊断信息,而尸检诊断出大部分颅面异常,应始终进行,作为产前成像的重要质量指标。
    The 22q11.2 deletion syndrome (22q11.2 DS) is known as the most common microdeletion syndrome. Due to its variable clinical phenotype, prenatal diagnosis can be challenging. The aim of this retrospective study was to evaluate the clinical course and pregnancy outcome of cases with prenatally diagnosed 22q11.2 deletion syndrome (DS) as well as to evaluate the role of prenatal magnetic resonance imaging (MRI) and postmortem examination. In total, 21 cases who underwent prenatal ultrasound examination and pregnancy care at the Department of Obstetrics and Gynecology at the Medical University of Vienna between 2012 and 2022 were included. The majority of the cases were genetically diagnosed using fluorescent in situ hybridization (FISH). The median gestational age (GA) at genetic diagnosis was 23.0 weeks (IQR 21.4-24.8 weeks). CHDs were detected in all fetuses and the most common extracardiac manifestation was thymus hypo/aplasia followed by genitourinary anomalies. Prenatal magnetic resonance imaging (MRI) revealed additional diagnostic information in three of ten cases. Overall, 14 patients opted for drug-induced TOP, of which 9 cases had a feticide prior to the induction of labor. The majority of craniofacial malformations were only detected by autopsy. In conclusion, the majority of cases prenatally diagnosed with 22q11.2 DS had an absent or hypoplastic thymus noted antenatally in addition to the detected CHD, and almost half of the cases had another extracardiac malformation of predominantly genitourinary origin. Furthermore, prenatal MRIs confirmed previously detected malformations, but only provided additional diagnostic information in three out of ten cases, whereas postmortem examination diagnosed most of the craniofacial anomalies and should always be conducted, serving as an important quality indicator for prenatal imaging.
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  • 文章类型: Journal Article
    结核病(TB)给尸检人员带来了巨大的健康风险,鉴于其结核病发病率比临床工作人员高3到5倍。这种风险在韩国尤为突出,报告称,2020年,经合组织成员国中结核病发病率最高,结核病死亡率排名第三。标准的结核病诊断方法,使用Ziehl-Neelsen染色对痰或组织进行抗酸杆菌(AFB)的组织病理学检查,需要以1000倍放大倍数对载玻片进行显微镜检查,这是劳动密集型和耗时的。本文提出了一种计算机辅助诊断(CAD)系统,旨在在小于1000×的放大倍数下提高TB诊断的效率。通过使用从30张训练幻灯片和10张评估幻灯片以400倍放大倍数拍摄的图像来训练9个神经网络,我们评估了他们检测结核分枝杆菌的能力.N模型达到了最高的精度,每个补丁99.77%,每个幻灯片90%。我们发现该模型可以帮助病理学家进行初步的结核病筛查,从而减少诊断时间。我们预计这项研究将有助于最大限度地减少尸检人员的感染风险,并迅速确定死亡原因。
    Tuberculosis (TB) presents a substantial health risk to autopsy staff, given its three to five times higher incidence of TB compared to clinical staff. This risk is notably accentuated in South Korea, which reported the highest TB incidence rate and the third highest TB mortality rate among OECD member countries in 2020. The standard TB diagnostic method, histopathological examination of sputum or tissue for acid-fast bacilli (AFB) using Ziehl-Neelsen staining, demands microscopic examination of slides at 1000× magnification, which is labor-intensive and time-consuming. This article proposes a computer-aided diagnosis (CAD) system designed to enhance the efficiency of TB diagnosis at magnification less than 1000×. By training nine neural networks with images taken from 30 training slides and 10 evaluation slides at 400× magnification, we evaluated their ability to detect M. tuberculosis. The N model achieved the highest accuracy, with 99.77% per patch and 90% per slide. We discovered that the model could aid pathologists in preliminary TB screening, thereby reducing diagnostic time. We anticipate that this research will contribute to minimizing autopsy staff\'s infection risk and rapidly determining the cause of death.
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  • 文章类型: Journal Article
    背景:先天性膈疝(CDH)与高死亡率和显著的肺部发病率相关。这项研究的目的是描述CDH患者尸检中观察到的组织病理学特征,并将其与临床表现相关联。
    方法:我们回顾性回顾了2017年至2022年7月8例CDH患者的死后发现和相应的临床特征。
    结果:中位生存时间为46(8-624)小时。尸检报告显示,弥漫性肺泡损伤(充血和出血)和透明膜形成是观察到的主要病理性肺改变。值得注意的是,尽管肺体积显著减少,50%的病例肺发育正常,3例(37.5%)存在分叶状畸形。所有患者均表现为大动脉导管未闭(PDA)和卵圆孔未闭,导致右心室(RV)体积增加,心肌纤维出现轻微充血和肿胀。肺血管显示动脉中膜和外膜增厚。肺发育不全和弥漫性肺损伤导致气体交换受损,而PDA和肺动脉高压导致RV衰竭,随后的器官功能障碍和最终死亡。
    结论:CDH患者通常会死于心肺衰竭,由病理生理因素的复杂相互作用驱动的状况。这种复杂性解释了对当前可用的血管扩张剂和通气疗法的不可预测的反应。
    Congenital diaphragmatic hernia (CDH) is associated with high mortality rates and significant pulmonary morbidities. The objective of this study was to delineate the histopathological features observed in necropsies of CDH patients and correlate these with their clinical manifestations.
    We retrospectively reviewed the postmortem findings and corresponding clinical characteristics in eight CDH cases from 2017 to July 2022.
    The median survival time was 46 (8-624) hours. Autopsy reports showed that diffuse alveolar damage (congestion and hemorrhage) and hyaline membrane formation were the primary pathological lung changes observed. Notably, despite significant reduction in lung volume, the lung development appeared normal in 50% of the cases, while lobulated deformities were present in three (37.5%) cases. All patients displayed a large patent ductus arteriosus (PDA) and a patent foramen ovale, resulting in increased right ventricle (RV) volume, and myocardial fibers appeared slightly congested and swollen. The pulmonary vessels indicated thickening of the arterial media and adventitia. Lung hypoplasia and diffuse lung damage resulted in impaired gas exchange, while PDA and pulmonary hypertension led to RV failure, subsequent organ dysfunction and ultimately death.
    Patients with CDH typically succumb to cardiopulmonary failure, a condition driven by a complex interplay of pathophysiological factors. This complexity accounts for the unpredictable response to currently available vasodilators and ventilation therapies.
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  • 文章类型: Journal Article
    背景:2019年冠状病毒病(COVID-19)已经成为一种大流行超过2年。尸检检查是了解新出现感染的发病机理及其随之而来的死亡率的宝贵工具。本研究的目的是介绍在约旦进行的COVID-19阳性尸检的肺部和心脏病理学发现。
    方法:该研究涉及法医学案例,死因不明确,法律规定进行尸检。我们纳入了死亡时COVID-19阳性病例的常规大体和显微镜检查的临床和病理结果。通过实时聚合酶链反应的分子检测确认了严重急性呼吸系统综合症冠状病毒2(SARS-CoV-2)的检测,IgM的血清学检测和肺样本的电子显微镜检查。
    结果:包括17次尸检,男性占主导地位(76.5%),约旦人(70.6%),50岁是死亡时的平均年龄。16例中有9例(56.3%)有合并症,一个案例缺乏这样的数据。肺组织组织学检查发现13/17例(76.5%)弥漫性肺泡损伤,肺微血栓8/17例(47.1%)。几乎没有检测到显微镜下的心脏发现。两名患者死于急性心脏病,肺部表现有限。
    结论:在尸检中发现SARS-CoV-2可能是偶然或共同的发现,这突出了尸检检查在有争议的病例中确定确切死亡原因的价值。
    BACKGROUND: Coronavirus disease 2019 (COVID-19) has emerged as a pandemic for more than 2 years. Autopsy examination is an invaluable tool to understand the pathogenesis of emerging infections and their consequent mortalities. The aim of the current study was to present the lung and heart pathological findings of COVID-19-positive autopsies performed in Jordan.
    METHODS: The study involved medicolegal cases, where the cause of death was unclear and autopsy examination was mandated by law. We included the clinical and pathologic findings of routine gross and microscopic examination of cases that were positive for COVID-19 at time of death. Testing for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was confirmed through molecular detection by real-time polymerase chain reaction, serologic testing for IgM and electron microscope examination of lung samples.
    RESULTS: Seventeen autopsies were included, with male predominance (76.5%), Jordanians (70.6%), and 50 years as the mean age at time of death. Nine out of 16 cases (56.3%) had co-morbidities, with one case lacking such data. Histologic examination of lung tissue revealed diffuse alveolar damage in 13/17 cases (76.5%), and pulmonary microthrombi in 8/17 cases (47.1%). Microscopic cardiac findings were scarcely detected. Two patients died as a direct result of acute cardiac disease with limited pulmonary findings.
    CONCLUSIONS: The detection of SARS-CoV-2 in postmortem examination can be an incidental or contributory finding which highlights the value of autopsy examination to determine the exact cause of death in controversial cases.
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