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“All things must pass” - Cutaneous migration of an endobronchial valve “一切都必须过去”-支气管内膜瓣膜的皮肤迁移
Pub Date : 2022-01-01 DOI: 10.1177/20542704221074148
Michelle Lee, R. Baranowski, David Gammon, J. Hargrave, D. Waller
Summary The Zephyr (PulmonX Inc., Redwood, CA) endobronchial valve (EBV), predominantly designed for lung volume reduction in emphysema, can also be used to close a spontaneous or post-operative prolonged air leak (PAL). We describe a previously unreported complication of cutaneous migration of an EBV, inserted for management of a PAL from a postoperative bronchopleural fistula (BPF), in a 62-year-old male following a right upper lobe posterior-apical (S1,2) segmentectomy. His PAL resulted in a chronic empyema which failed to respond to surgical debridement, anterior cavernostomy and pectoral myoplasty. Bronchoscopic closure of the air leak by EBV insertion resulted in clinical improvement but there was a residual chronic wound sinus through which the patient reported protrusion of a foreign body that was causing irritation. It was the EBV. We hypothesise that the BPF healed beneath the EBV causing it to dislodge but its route to the skin remains a mystery.
Zephyr (PulmonX Inc., Redwood, CA)支气管内瓣膜(EBV)主要用于肺气肿的肺体积减小,也可用于关闭自发性或术后延长的空气泄漏(PAL)。我们描述了一个以前未报道的EBV皮肤迁移的并发症,在62岁男性右上叶后根尖(S1,2)节段切除术后插入EBV用于治疗术后支气管胸膜瘘(BPF)引起的PAL。他的PAL导致慢性脓胸,手术清创、前海绵体造口术和胸肌成形术均无效。支气管镜下通过EBV插入封闭漏气导致临床改善,但有一个残留的慢性伤口窦,患者报告异物突出,引起刺激。是EBV。我们假设BPF在EBV下面愈合,导致EBV脱落,但它进入皮肤的途径仍然是个谜。
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引用次数: 1
Benign metastasizing leiomyoma - a case of benign metastasis. 良性转移性子宫肌瘤--一例良性转移病例。
Pub Date : 2021-12-13 eCollection Date: 2021-12-01 DOI: 10.1177/20542704211064482
Diogo André, Fabiana Gouveia, Helena Luís, Mónica Caldeira, Filipe Perneta, Marília Jeanette Gonçalves, António José Chaves

Leiomyomas are benign tumours of smooth muscle cells that most often affect the female genital tract, but their metastasis to extra-uterine locations represent rare, yet misunderstood phenomena. The authors present a clinical case of a 42-year-old woman, who underwent a hysterectomy 15 years ago due to myomas, admitted with multiple pulmonary nodules and abdominal mass, diagnosed by imaging tests, in the context of haemoptysis. The anatomopathological exams of the pulmonary and abdominal lesions were compatible with the diagnosis of benign metastatic leiomyoma. Benign metastatic leiomyoma is a rare condition that particularly affects women of childbearing age, with a history of hysterectomy for uterine fibroids. Hence, this entity must be considered in the differential diagnosis of women with pulmonary nodules of uncertain aetiology.

子宫肌瘤是由平滑肌细胞组成的良性肿瘤,最常见于女性生殖道,但其转移到子宫外部位的现象非常罕见,但也存在误解。作者介绍了一例临床病例,患者是一名 42 岁女性,15 年前因子宫肌瘤接受了子宫切除术,入院时经影像学检查确诊为多发性肺结节和腹部肿块,并伴有咯血。肺部和腹部病变的解剖病理学检查符合良性转移性子宫肌瘤的诊断。良性转移性子宫肌瘤是一种罕见的疾病,尤其影响育龄妇女和曾因子宫肌瘤切除子宫的妇女。因此,在对病因不确定的肺结节进行鉴别诊断时,必须考虑到这一实体。
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引用次数: 0
Massive haemorrhage: an unusual presentation of systemic lupus erythematosus. 大出血:系统性红斑狼疮的不寻常表现。
Pub Date : 2021-11-30 eCollection Date: 2021-11-01 DOI: 10.1177/20542704211062041
Wajeeha Qayyum, Sohail Khan, Muhammad Shahid Iqbal, Muhammad Fozan Khan, Zaland Ahmed Yousafzai, Saima Afaq

Systemic lupus erythematosus (SLE) usually affects young females and its presentation with haemorrhage is unusual. Intracerebral bleed (ICB) has been described in a few case reports, but massive haematuria has not been reported in the literature so far. Here, we present a case of a 56 year-old-lady who presented with expanding lobar bleed and massive haematuria as the first presentation of SLE secondary to vasculitis. Lupus vasculitis usually presents with thrombosis-related complications and although bleeding in this context is rare, it can lead to catastrophic consequences. Hence, vasculitis-related bleeding should be taken under consideration in a challenging situation like ours.

系统性红斑狼疮(SLE)通常影响年轻女性,其表现为出血是罕见的。脑出血(ICB)已在少数病例报告中被描述,但大量血尿尚未在文献中报道。在这里,我们报告一位56岁的女性,她以扩大的大叶出血和大量血尿作为继发于血管炎的SLE的首次表现。狼疮血管炎通常表现为血栓相关并发症,虽然出血在这种情况下是罕见的,但它可以导致灾难性的后果。因此,在像我们这样具有挑战性的情况下,血管炎相关出血应该被考虑在内。
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引用次数: 0
The neurological risks of playing association football. 参加协会足球的神经风险。
Pub Date : 2021-11-18 eCollection Date: 2021-11-01 DOI: 10.1177/20542704211055558
Oliver C Cockerell, Natalie Iino Hayes, Richard Sylvester

Aims: The present study aims to provide a narrative review of the literature surrounding concussion and head injury in football and its clarity in evaluating the risk of long-term neurological disease.

Findings: Epidemiological studies have shown correlations between participation in professional football and increased incidence of neurodegenerative disease and there have been reports of chronic traumatic encephalopathy (CTE) in the brains of former players in autopsy. These findings have been assumed by some to be the result of repetitive brain injury from head injuries and/or from heading the ball over a player's career. Data linking increased heading exposure with dementia is conflicting, and studies are limited by the reliance on retrospection and undocumented reports of concussion. It remains unclear whether CTE is unique to sportsmen or a variant of dementia pathology endemic in the population.

Conclusions: Although logically appealing, there is no current evidence that heading is the cause of neurodegeneration amongst footballers and risks should be balanced by the protective mental and physical benefits of the sport. Physicians have an important role in providing balanced views in this emotive and controversial area.

目的:本研究旨在对有关足球运动员脑震荡和头部损伤的文献进行综述,并对其在评估长期神经系统疾病风险方面的清晰性进行综述。研究结果:流行病学研究表明,参加职业足球运动与神经退行性疾病发病率增加之间存在相关性,并且有报道称,在尸检中,前球员的大脑中存在慢性创伤性脑病(CTE)。一些人认为,这些发现是由于球员在职业生涯中头部受伤和/或头球造成的反复脑损伤的结果。将头球暴露增加与痴呆联系起来的数据是相互矛盾的,而且研究依赖于回顾性研究和未记录的脑震荡报告,因此受到限制。目前尚不清楚CTE是运动员独有的还是人群中痴呆病理的一种变体。结论:虽然逻辑上很吸引人,但目前还没有证据表明头球是足球运动员神经退化的原因,这项运动的保护精神和身体利益应该平衡风险。在这个情绪化和有争议的领域,医生在提供平衡的观点方面发挥着重要作用。
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引用次数: 3
Clinical frailty as a key characteristic of the patient population of the NHS Nightingale North West COVID-19 temporary emergency field hospital: cohort study April to June 2020. 临床虚弱是NHS南丁格尔西北COVID-19临时紧急野战医院患者人群的一个关键特征:2020年4月至6月的队列研究
Pub Date : 2021-10-05 eCollection Date: 2021-10-01 DOI: 10.1177/20542704211046435
M Trent Herdman, Tim Seers, Cassandra Ng, Rebecca Davenport, Sarah Sibley, Steve Mannion, Sooria Balasegaram, Anthony D Redmond

Objectives: COVID-19 temporary emergency 'field' hospitals have been established in the UK to support the surge capacity of the National Health Service while protecting the community from onward infection. We described the population of one such hospital and investigated the impact of frailty on clinical outcomes.

Design: Cohort study.

Setting: NHS Nightingale Hospital North West, April-June 2020.

Participants: All in-patients with COVID-19.

Main outcome measures: Mortality and duration of admission.

Methods: We analysed factors associated with mortality using logistic regression and admission duration using Cox's regression, and described trends in frailty prevalence over time using linear regression.

Results: A total of 104 COVID-19 patients were admitted, 74% with moderate-to-severe frailty (clinical frailty score, CFS > 5). A total of 84 were discharged, 14 transferred to other hospitals, and six died on site. High C-reactive protein (CRP) > 50 mg/dL predicted 30-day mortality (adjusted odds ratio 11.9, 95%CI 3.2-51.5, p < 0.001). Patients with CFS > 5 had a 10-day median admission, versus 7-day for CFS ≤ 5 and half the likelihood of discharge on a given day (adjusted hazard ratio 0.51, 95%CI 0.29-0.92, p  =  0.024). CRP > 50 mg/dL and hospital-associated COVID-19 also predicted admission duration. As more frail patients had a lower rate of discharge, prevalence of CFS > 5 increased from 64% initially to 90% in the final week (non-zero slope p < 0.001). Conclusions: The NNW population was characterized by high levels of frailty, which increased over the course of the hospital's operation, with subsequent operational implications. Identifying and responding to the needs of this population, and acknowledging the risks of this unusual clinical context, helped the hospital to keep patients safe.

目标:英国已经建立了COVID-19临时紧急“现场”医院,以支持国家卫生服务的激增能力,同时保护社区免受进一步感染。我们描述了一家这样的医院的人群,并调查了虚弱对临床结果的影响。设计:队列研究。环境:NHS南丁格尔医院西北,2020年4月至6月。参与者:所有新冠肺炎住院患者。主要结局指标:死亡率和住院时间。方法:我们使用逻辑回归分析了与死亡率相关的因素,使用Cox回归分析了入院时间,并使用线性回归描述了虚弱患病率随时间的趋势。结果:共收治104例COVID-19患者,其中74%为中重度虚弱(临床虚弱评分,CFS > 5)。84人出院,14人转院,6人当场死亡。高c -反应蛋白(CRP) > 50 mg/dL预测30天死亡率(校正优势比11.9,95%CI 3.2-51.5, p = 5),中位住院时间为10天,而CFS≤5的中位住院时间为7天,且在某一天出院的可能性为一半(校正风险比0.51,95%CI 0.29-0.92, p = 0.024)。CRP > 50mg /dL和医院相关的COVID-19也预测住院时间。由于体弱患者越多,出院率越低,CFS > 5的患病率从最初的64%上升到最后一周的90%(斜率非零p)。结论:NNW人群的特点是体弱程度高,在医院运营过程中,体弱程度增加,随后的运营影响。识别和应对这一人群的需求,并认识到这种不同寻常的临床环境的风险,有助于医院保证患者的安全。
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引用次数: 1
Achenbach's syndrome: a rare condition. 阿肯巴赫综合征:一种罕见的疾病。
Pub Date : 2021-09-20 eCollection Date: 2021-09-01 DOI: 10.1177/20542704211047121
Carlos I Higuera-Cetina, Lina M Montaña-Gómez, Yelson A Picón-Jaimes, Javier E Orozco-Chinome, Iván Lozada-Martínez, Luis R Moscote-Salazar

Achenbach's syndrome corresponds to a pathology characterized by the appearance of ecchymoses and bruises on the fingers of the hands and eventually on the feet. It is a benign and self-limited disease, which is accompanied by pain. It generates great concern because its sudden appearance leads women who are the most affected to consult the emergency services. At present, its pathophysiology is unknown and requires knowledge of the disease to diagnose it. It is a must for poorly trained professionals.

阿肯巴赫综合征的病理特征是手指上出现瘀斑和瘀伤,最终出现在脚上。它是一种良性、自限性疾病,伴有疼痛。它引起了极大的关注,因为它的突然出现导致受影响最严重的妇女咨询紧急服务。目前,其病理生理尚不清楚,需要了解疾病的知识才能进行诊断。对于缺乏训练的专业人员来说,这是必须的。
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引用次数: 4
Hemi-paraplegia and hemi-anaesthesia in the inflammatory bowel disease clinic. 炎症性肠病临床的半截瘫和半麻醉。
Pub Date : 2021-08-31 eCollection Date: 2021-09-01 DOI: 10.1177/20542704211035987
Hesam Ahmadi Nooredinvand, Anu Vallipuram, Alice Dawson, Jaymin Patel, Waqar Rashid, Andrew Poullis
In this case report, we present a rare case of central nervous system demyelination secondary to infliximab therapy. A 47-year-old gentleman with a 15-year history of left sided ulcerative colitis presented to the gastroenterology clinic with a 1-month history of bloody diarrhoea associated with a significantly elevated faecal calprotectin. A trial of oral and rectal mesalazine as well as oral steroids proved ineffective. He had previously been intolerant to both Azathioprine and 6-mercaptopurine. Decision was made to escalate his treatment to methotrexate and infliximab 5 mg/kg (originator). He was managed in the outpatient setting and did not require hospitalization. First infliximab infusion was given on 14 May 2020. Second and third infusion were given two and six weeks after respectively. One week prior to the third infusion, he began to develop tingling and numbness down the right side of his body and he felt his right foot was more sensitive to changes in temperature. His Methotrexate was stopped but it was decided to proceed with giving the third infusion of infliximab. In the following two weeks he then developed weakness in the left leg and reported urinary hesitancy. He was reviewed in the ambulatory unit by the neurologist twelve days following the start of his neurological symptoms. On clinical examination, cranial nerves were intact. He had good muscle bulk and no focal wasting. Tone was normal bilaterally, but power was mildly reduced on the left, 4/5 in wrist, digits, hip flexion and knee extension. Reflexes were present bilaterally, but the supinator, knee and ankle reflexes were brisk on the left. Coordination was intact. There was reduced proprioception and temperature sensation on the right side, with a sensory level just below the clavicle, whilst touch, vibration and two-point discrimination were preserved bilaterally. Plantars were downgoing bilaterally. An urgent MRI of the spine was subsequently arranged which revealed a right sided intramedullary cord lesion at C4 with some focal eccentric enhancement (Figure 1). A subsequent MRI of his head revealed white matter plaques in the cerebral hemisphere and corpus callosum (Figure 2). The post contrast sequences (not shown) showed no features of active demyelination. CSF analysis was positive for IgG oligoclonal bands. Serum oligoclonal band testing revealed no abnormalities. These findings supported a diagnosis of Brown-Sequard syndrome secondary to a cord lesion due to multiple sclerosis (MS). The diagnosis of MS was based on evidence of widespread inflammation in the brain and the spinal cord in addition to positive oligoclonal bands in the CSF, which can be used as criteria for dissemination in time (2017 revised McDonald criteria). His infliximab was discontinued after his third infusion with no deterioration to his colitis and his neurology gradually started to improve two weeks later. He had a further flare of his MS a few months later manifesting as diplopia. Repeat MR
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引用次数: 1
Hansen's disease - a forgotten disease? 汉森氏病——被遗忘的疾病?
Pub Date : 2021-08-30 eCollection Date: 2021-08-01 DOI: 10.1177/20542704211035995
Paula Marques Ferreira, Inês Rueff Rato, Joana Rigor, Margarida Mota

Hansen's disease, also known as leprosy, is an infection caused by the bacteria Mycobacterium leprae. The authors present the case of a 52-year-old man, born in Tondela and living in Espinho, with no pathological antecedents. The clinical picture began in April 2017, when macular lesions appeared in the lower limbs and rapidly progressed to the trunk and upper limbs, associated with complaints of pruritus but without alterations in the analytical study. After several topical and systemic treatments with glucocorticoids, antifungals, antibacterials and unsuccessful antihistamines, he was referred to an external consultation of Dermatology. He performed a biopsy of one of the lesions that revealed the definitive diagnosis: "Lepromatous Leprosy". After the biopsy result, he started triple treatment with rifampicin, clofazimine and dapsone with improvement of the condition.

汉森病,也被称为麻风病,是一种由麻风分枝杆菌引起的感染。作者提出了一名52岁男子的病例,出生在通德拉,居住在埃斯皮尼奥,没有病理前例。临床表现始于2017年4月,当时黄斑病变出现在下肢,并迅速进展到躯干和上肢,与瘙痒的主诉相关,但分析研究中没有改变。在用糖皮质激素、抗真菌药、抗菌药和抗组胺药进行了几次局部和全身治疗后,他被转到皮肤科的外部会诊。他对其中一个病变进行了活检,明确诊断为“麻风性麻风病”。活检结果出来后,开始利福平、氯法齐明、氨苯砜三联治疗,病情有所好转。
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引用次数: 0
Myocardial infarction post COVID-19 vaccine - coincidence, Kounis syndrome or other explanation - time will tell. COVID-19疫苗后心肌梗死-巧合,库尼斯综合征或其他解释-时间会告诉我们。
Pub Date : 2021-08-11 eCollection Date: 2021-08-01 DOI: 10.1177/20542704211025259
Ossama Maadarani, Zouheir Bitar, Mahmoud Elzoueiry, Mohammad Nader, Mohamad Abdelfatah, Tamer Zaalouk, Mohamad Mohsen, Mohamad Elhabibi

A case of ST elevation myocardial infarction reported post Coronavirus disease 2019 (COVID-19) vaccine. Probably premature to draw a link between COVID-19 vaccine and myocardial infarction.

2019冠状病毒病(COVID-19)疫苗接种后ST段抬高型心肌梗死1例将COVID-19疫苗与心肌梗死联系起来可能为时过早。
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引用次数: 26
Double heart - chronic large missed pseudoaneurysm of left ventricle. 双心-慢性大的左心室假性动脉瘤。
Pub Date : 2021-07-08 eCollection Date: 2021-07-01 DOI: 10.1177/20542704211025258
Ossama Maadarani, Zouheir Bitar, Ragab Elshabasy, Tamer Zaalouk, Mohamad Mohsen, Mahmoud Elzoueiry, Mohamad Abdelfatah, Mohamad Elhabibi, Mohamad Gohar

Myocardial infarction is considered the most common cause of left ventricular pseudoaneurysm. Large missed pseudoaneurysm of the left ventricle incidentally diagnosed and treated conservatively.

心肌梗塞被认为是左心室假性动脉瘤最常见的原因。大面积遗漏的左心室假性动脉瘤偶然诊断和保守治疗。
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引用次数: 0
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