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Orbital Emphysema as a Consequence of Forceful Nose-Blowing: Report of a Case 强力擤鼻导致眼眶肺气肿1例报告
Pub Date : 2019-06-18 DOI: 10.1155/2019/4383086
Yukino Ariyoshi, H. Naito, T. Yumoto, Atsuyoshi Iida, Hirotsugu Yamamoto, N. Fujisaki, T. Aokage, K. Tsukahara, Taihei Yamada, Y. Mandai, T. Osako, A. Nakao
Orbital emphysema occurs when air enters the soft tissue surrounding the orbit. Although orbital blowout fractures are often caused by face trauma, nontraumatic orbital fractures can also occur but have been rarely described. Here, a case of orbital and palpebral emphysema caused by forceful nose-blowing is presented. Examination uncovered gross swelling of the right eye and discernable subcutaneous emphysema. The patient had normal eye movement and visual acuity. Orbital computed tomography (CT) revealed orbital emphysema secondary to an orbit floor fracture into the maxillary sinus, resulting from high intranasal pressure upon blowing her nose. The patient received conservative management with antibiotics and was given instructions not to sneeze or blow her nose. She fully recovered and all her symptoms completely resolved.
当空气进入眼眶周围的软组织时,就会发生眼眶肺气肿。虽然眼眶爆裂骨折常由面部外伤引起,但非创伤性眼眶骨折也可能发生,但很少有报道。本文报告一例因强力擤鼻而引起的眼眶及眼睑肺气肿。检查发现右眼明显肿胀,可见皮下肺气肿。患者眼动正常,视力正常。眼眶计算机断层扫描(CT)显示眼眶肺气肿继发于眼眶底骨折进入上颌窦,由擤鼻时鼻内高压引起。患者接受抗生素保守治疗,并被告知不要打喷嚏或擤鼻涕。她完全康复了,所有的症状都完全消失了。
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引用次数: 7
Traumatic Takotsubo Cardiomyopathy in a Patient with Extensive Coronary Artery Disease 广泛冠状动脉疾病患者的外伤性Takotsubo心肌病
Pub Date : 2019-06-12 DOI: 10.1155/2019/7270426
Abagayle E Renko, Warren C. Doyle, Paul W. Sokoloski
Takotsubo Cardiomyopathy (TCM) should be considered in the differential diagnosis for patients with cardiovascular symptoms not only following emotional trauma but also following motor vehicle accidents. A 45-year-old woman presented with chest pain following a motor vehicle accident. While she had an elevated troponin level and an extensive history of cardiac disease, her electrocardiogram was normal. Echocardiogram, however, demonstrated transiently reduced left ventricular systolic function with mid to apical hypokinesis consistent with TCM. We emphasize the use of a diagnostic score and point of care focused cardiac ultrasound (FOCUS) to expedite the recognition, evaluation, and treatment of suspected TCM in an Emergency Department setting.
无论是情绪创伤后的心血管症状患者,还是机动车事故后的心血管症状患者,均应考虑Takotsubo心肌病(TCM)的鉴别诊断。一名45岁女性在机动车事故后出现胸痛。虽然她有肌钙蛋白水平升高和广泛的心脏病史,但她的心电图正常。然而,超声心动图显示短暂性左心室收缩功能减弱,中至根尖运动减弱,与中医一致。我们强调在急诊科使用诊断评分和护理点心脏超声(FOCUS)来加快对疑似中医的识别、评估和治疗。
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引用次数: 1
A Case of Acute Myocardial Infarction in a Patient Whose Initial Complaints Were Hematemesis and Epigastric Discomfort. 一例最初主诉为吐血和胃上不适的急性心肌梗死患者。
Pub Date : 2019-05-23 eCollection Date: 2019-01-01 DOI: 10.1155/2019/5984251
Kazuhiko Omori, Youichi Yanagawa

The patient was a 64-year-old woman with systemic lupus erythematosus, thrombophlebitis of the lower legs, cerebral infarction with left hemiparesis, and colostomy after perforation of the sigmoid colon. On the morning of her presentation, the patient felt epigastric abnormality. Thereafter, hematemesis occurred twice, leading her to call an ambulance in the afternoon. Upon arrival, electrocardiography before securing a venous route and obtaining blood samples revealed ST segment elevation in leads II, III, and aVF. As her vital signs were stable and her hemoglobin level had decreased by just 1.1 g/dl in comparison to the previous day, emergency coronary angiography (CAG) was performed. CAG revealed complete occlusion at section #4. She underwent right coronary angioplasty with stent placement. The patient's course after angioplasty was uneventful. On the 15th hospital day, esophagogastroduodenoscopy revealed esophageal erosion and superficial gastritis. She was discharged on foot the following day. When physicians treat patients with hematemesis, electrocardiography and the measurement of troponin are essential before esophagogastroduodenoscopy.

患者是一名64岁的女性,患有系统性红斑狼疮、下肢血栓性静脉炎、脑梗死伴左偏瘫和乙状结肠穿孔后结肠造口。在她出现症状的当天早上,患者感到上腹部异常。此后,她出现了两次吐血,导致她在下午叫了救护车。抵达后,在确定静脉通路和获取血液样本之前进行的心电图检查显示,导联II、III和aVF的ST段抬高。由于她的生命体征稳定,血红蛋白水平与前一天相比仅下降了1.1 g/dl,因此进行了紧急冠状动脉造影(CAG)。CAG显示第4节完全闭塞。她接受了右冠状动脉血管成形术和支架置入术。患者血管成形术后的病程平静。第15个住院日,食管胃十二指肠镜检查显示食管糜烂和浅表性胃炎。第二天她步行出院了。当医生治疗吐血患者时,在食管胃十二指肠镜检查之前,心电图和肌钙蛋白的测量是必不可少的。
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引用次数: 0
Case of Nontraumatic Rectus Sheath Hematoma from Muscle Training Mimicking Acute Abdomen. 模拟急腹症肌肉训练所致非外伤性直肌鞘血肿1例。
Pub Date : 2019-05-23 eCollection Date: 2019-01-01 DOI: 10.1155/2019/3158969
Yukino Ariyoshi, Hiromichi Naito, Hiromi Ihoriya, Tetsuya Yumoto, Noritomo Fujisaki, Kohei Tsukahara, Taihei Yamada, Yasuhiro Mandai, Takaaki Osako, Atsunori Nakao

Rectus sheath hematoma is an unusual but well-known clinical problem. Our hospital admitted a 54-year-old woman complaining of harsh right-sided hypogastric pain that started while muscle training. Computed tomography of the abdomen and pelvis demonstrated a right rectus sheath hematoma. As the hematoma did not increase, the patient was conservatively treated. Despite increased awareness of rectus sheath hematoma, its early diagnosis and treatment still present a challenge to emergency physicians. Swift acknowledgement of this rare cause of abdominal pain may avoid more intrusive examination, unnecessary hospitalization, and laparotomy. Careful consideration of the patient's medical history and a high index of suspicion are needed to diagnose this complication.

直肌鞘血肿是一种罕见但众所周知的临床问题。我们医院收治了一名54岁的女性,她抱怨在肌肉训练时开始出现严重的右侧下腹疼痛。腹部及骨盆电脑断层显示右侧直肌鞘血肿。由于血肿未增加,患者接受保守治疗。尽管人们对直肌鞘血肿的认识不断提高,但其早期诊断和治疗仍然是急诊医生面临的挑战。迅速确认这种罕见的腹痛原因可以避免更多的侵入性检查,不必要的住院治疗和剖腹手术。诊断这种并发症需要仔细考虑患者的病史和高度怀疑。
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引用次数: 5
Expression of Concern on "Late Onset Traumatic Diaphragmatic Herniation Leading to Intestinal Obstruction and Pancreatitis: Two Separate Cases". “迟发性外伤性膈疝导致肠梗阻和胰腺炎:两例独立病例”的关注表达。
Pub Date : 2019-05-22 eCollection Date: 2019-01-01 DOI: 10.1155/2019/6917081
Case Reports In Emergency Medicine
Case Reports in Emergency Medicine would like to express concern with the article titled “Late Onset Traumatic Diaphragmatic Herniation Leading to Intestinal Obstruction and Pancreatitis: Two Separate Cases” published in Case Reports in Emergency Medicine in August 2015 [1], as the article was published without the approval of Dr. Baris D. Yildiz and his name was missing from the authors’ list. An institutional investigation claimed Dr. Yildiz waived his right to be an author, which he disputed. A court of Intellectual and Industrial Property Rights in Turkey ruled thatDr. Yildiz should be listed as co-author, whichwas upheld at appeal. However, Dr. Yildiz did not agree to a corrigendum listing him as an author. Additionally, the editorial office was contacted by someone saying they were the legal representative of one of the patients and they had not consented to publication. However, the representative’s identity was not verified and they did not respond to queries.
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引用次数: 1
Two Rare Cases of Appendicitis: Amyand's Hernia and De Garengeot's Hernia. 两例罕见阑尾炎:Amyand疝和De Garengeot疝。
Pub Date : 2019-04-16 eCollection Date: 2019-01-01 DOI: 10.1155/2019/6759206
Kimberly A Schaaf, Eric M Melnychuk, Ross D Ellison, Amy J Snover

An Amyand's hernia is an inguinal hernia that contains vermiform appendix. De Garengeot's hernias are similar; however, in this case the appendix is within a femoral hernia. Both types of hernia are rare, and those hernias associated with appendicitis, perforation, or abscess are even scarcer presentations. The treatment of Amyand's hernia and De Garengeot's hernia is not standardized. Generally, hernia repair is performed but disagreement remains regarding the use of mesh and performing appendectomy. This case series describes two individuals with appendicitis presenting to one emergency department within a 24-hour time frame. One case is of a patient with Amyand's hernia and another case is a patient with De Garengeot's hernia with an adjacent abscess. Both individuals were managed with appendectomy and hernia repair without the use of mesh.

Amyand疝是一种包含蚓状阑尾的腹股沟疝。德·加朗乔的疝气也是类似的;然而,在这种情况下,阑尾位于股疝内。这两种类型的疝气都很少见,而那些伴有阑尾炎、穿孔或脓肿的疝气更少见。Amyand疝气和De Garengeot疝气的治疗没有标准化。一般来说,疝气修补术被实施,但关于使用补片和实施阑尾切除术的分歧仍然存在。本病例系列描述了两个个体阑尾炎呈现在一个急诊室24小时内的时间框架。一个病例是Amyand疝气患者,另一个病例是De Garengeot疝气患者,旁边有脓肿。两例患者均行阑尾切除术和疝修补术,未使用补片。
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引用次数: 8
Acute Onset of Hypersomnolence and Aphasia Secondary to an Artery of Percheron Infarct and a Proposed Emergency Room Evaluation. 继发于高位动脉梗死的嗜睡和失语的急性发作和建议的急诊室评估。
Pub Date : 2019-04-08 eCollection Date: 2019-01-01 DOI: 10.1155/2019/1260865
Tamra Ranasinghe, SoHyun Boo, Amelia Adcock

Artery of Percheron (AOP) is a rare anatomical variant, which supplies bilateral paramedian thalami and the rostral mesencephalon via a single dominant thalamic perforating artery arising from the P1 segment of a posterior cerebral artery. AOP infarcts can present with a plethora of neurological symptoms: altered mental status, memory impairment, hypersomnolence, coma, aphasia, and vertical gaze palsy. Given the lack of classic stroke signs, majority of AOP infarcts are not diagnosed in the emergency setting. Timely diagnosis of an acute bilateral thalamic infarct can be challenging, and this case report highlights the uncommon neurological presentation of AOP infarction. The therapeutic time window to administer IV tPA can be missed due to this delay in diagnosis, resulting in poor clinical outcomes. To initiate appropriate acute ischemic stroke management, we propose a comprehensive radiological evaluation in the emergency room for patients with a high suspicion of an AOP infarction.

脑后动脉(AOP)是一种罕见的解剖变异,它通过一条从大脑后动脉P1段产生的丘脑显性穿通动脉供应双侧丘脑旁正中和中脑吻侧。AOP梗死可表现为大量的神经系统症状:精神状态改变、记忆障碍、嗜睡、昏迷、失语和垂直凝视性麻痹。由于缺乏典型的卒中征象,大多数AOP梗死不能在急诊环境中诊断出来。及时诊断急性双侧丘脑梗死可能具有挑战性,本病例报告强调AOP梗死的罕见神经学表现。由于这种诊断延误,可能错过静脉注射tPA的治疗时间窗口,导致临床结果不佳。为了启动适当的急性缺血性卒中管理,我们建议在急诊室对高度怀疑AOP梗死的患者进行全面的放射学评估。
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引用次数: 5
Novel Method for Removing Embedded Cactus Spines in the Emergency Department. 急诊部去除仙人掌内埋刺的新方法。
Pub Date : 2019-04-08 eCollection Date: 2019-01-01 DOI: 10.1155/2019/6062531
Andrew M Ford, Steven T Haywood, Douglas R Gallo

Injuries from cactus spines can present challenges to Emergency Medicine providers. When the patient has mental limitations that prevent cooperation with removal, these challenges grow. Traditional removal techniques have several drawbacks including prolonged time for complete removal and incomplete removal. We present the case of a 22-year-old with a history of low-functioning autism and congenital motor dysfunction with a cactus spine injury to a large surface area of her chest, abdomen, and extremities. Conscious sedation utilizing intramuscular ketamine and Operating Room (OR) hair removal mitts were utilized to quickly and effectively remove the cactus spines. The patient had efficient, painless resolution of her injury without need for additional spine removal.

仙人掌刺造成的伤害对急诊医疗人员来说是一个挑战。当患者有精神障碍,无法配合摘除时,这些挑战就会增加。传统的脱除技术存在完全脱除时间长、不完全脱除等缺点。我们报告一个22岁的病例,她有低功能自闭症和先天性运动功能障碍的病史,胸部、腹部和四肢的大面积仙人掌脊柱损伤。利用肌注氯胺酮和手术室脱毛手套进行有意识镇静,以快速有效地去除仙人掌刺。患者的损伤得到了有效、无痛的解决,无需额外的脊柱切除。
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引用次数: 0
Haloperidol-Induced Dystonia due to Sedation for Upper Gastrointestinal Endoscopy: A Pediatric Case Report. 氟哌啶醇引起的上消化道内窥镜镇静引起的肌张力障碍:一个儿科病例报告。
Pub Date : 2019-03-27 eCollection Date: 2019-01-01 DOI: 10.1155/2019/3591258
Kazufumi Yaginuma, Masahiro Watanabe, Kyohei Miyazaki, Atsushi Ono, Hiromichi Murai, Maki Nodera, Yuichi Suzuki, Kazuhide Suyama, Yukihiko Kawasaki, Mitsuaki Hosoya

Dystonia is a movement disorder characterized by sustained muscle tone. Antipsychotic agents sometimes cause acute dystonia that can rapidly worsen within a few hours or days. Because healthy children rarely receive antipsychotic agents, it is unusual to see antipsychotic agent-induced dystonia in pediatric emergency departments. We report a rare case of a 12-year-old healthy boy who presented with acute dystonia after administration of haloperidol for sedation. He was suspected of laryngeal dystonia because stridor and desaturation were present. The symptoms disappeared with the administration of hydroxyzine. Rapid diagnosis was important in this case because laryngeal dystonia is a potential life-threatening complication due to upper airway obstruction. Considering the risk of side effects, doctors who are not accustomed to administering pediatric anesthesia should consult a pediatrician and/or an anesthesiologist prior to administration of anesthetics to pediatric patients.

肌张力障碍是一种以持续的肌肉张力为特征的运动障碍。抗精神病药物有时会引起急性肌张力障碍,并在几小时或几天内迅速恶化。由于健康儿童很少接受抗精神病药物治疗,所以在儿科急诊科很少看到抗精神病药物引起的肌张力障碍。我们报告一个罕见的情况下,一个12岁的健康男孩谁提出急性肌张力障碍后给予氟哌啶醇镇静。他被怀疑喉张力障碍,因为喘鸣和去饱和存在。服用羟嗪后症状消失。快速诊断在这个病例中很重要,因为喉张力障碍是一个潜在的危及生命的并发症,由于上气道阻塞。考虑到副作用的风险,不习惯使用儿科麻醉的医生在给儿科患者使用麻醉药前应咨询儿科医生和/或麻醉师。
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引用次数: 4
Retracted: Marathon Runner with Acute Hyponatremia: A Neurological Disorder. 撤稿:马拉松运动员急性低钠血症:一种神经系统疾病。
Pub Date : 2019-03-26 eCollection Date: 2019-01-01 DOI: 10.1155/2019/3954675
Case Reports In Emergency Medicine

[This retracts the article DOI: 10.1155/2012/342760.].

[本文撤回文章DOI: 10.1155/2012/342760]。
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引用次数: 0
期刊
Case Reports in Emergency Medicine
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