999精品在线视频,手机成人午夜在线视频,久久不卡国产精品无码,中日无码在线观看,成人av手机在线观看,日韩精品亚洲一区中文字幕,亚洲av无码人妻,四虎国产在线观看 ?

Posterior reversible leukoencephalopathy syndrome presenting in a post-partum, 25-year-old-female with concomitant subarachnoid hemorrhage

2014-03-22 03:43:28DanielAronovichKirstenRitchieAlexanderScumpia
Journal of Acute Disease 2014年3期

Daniel M. Aronovich, Kirsten L. Ritchie, Alexander J. Scumpia

1Mount Sinai Medical Center, Department of Emergency Medicine, 4300 Alton Road, Miami Beach, FL 33140, U.S.A

2Memorial Regional Hospital, Department of Emergency Services, 3501 Johnson Street, Hollywood, FL 33021, U.S.A

Posterior reversible leukoencephalopathy syndrome presenting in a post-partum, 25-year-old-female with concomitant subarachnoid hemorrhage

Daniel M. Aronovich1, Kirsten L. Ritchie1, Alexander J. Scumpia2*

1Mount Sinai Medical Center, Department of Emergency Medicine, 4300 Alton Road, Miami Beach, FL 33140, U.S.A

2Memorial Regional Hospital, Department of Emergency Services, 3501 Johnson Street, Hollywood, FL 33021, U.S.A

Hincheyet al., first described that posterior reversible leukoencephalopathy syndrome has having a unique neuroradiographical finding of vasogenic edema and clinical symptoms including headache, altered mental status, seizure and visual disturbances in 1996. We present a rare case of posterior reversible leukoencephalopathy syndrome in a 2-week, post-partum G2P2A0 (normal spontaneous vaginal delivery at forty-weeks, without complications) 25-year-old-female with subarachnoid hemorrhage.

ARTICLE INFO

Article history:

Received 5 December 2014

Received in revised form 19 December 2014

Accepted 31 December 2014

Available online

Posterior reversible

1. Introduction

We present a rare case of posterior reversible leukoencephalopathy syndrome (PRES) in a 2-week, postpartum G2P2A0 (normal spontaneous vaginal delivery at forty-weeks, without complications) 25-year-old-female with subarachnoid hemorrhage.

2. Case presentation

The patient did not have a significant past medical/ surgical history. She presented with her husband via ambulance with a chief complaint of seizure. This newonset, convulsive episode described by her husband as upper and lower extremity “jerking motions” lasted for approximately 10 min and was aborted via 2 mg intravenous lorazepam administered by the paramedics in the field. Upon emergency department arrival, the patient’s vitals were: blood pressure with 165/117 mm Hg, HR 124 bpm, RR 22, afebrile, SpO2 99% on two liters nasal cannula, 116 mg/dL of finger stick glucose. On physical examination, the patient was hypertensive, alert and oriented×3, protecting her airway, tachycardic, incontinent of urine with complaints of a dull headache and bilateral blurry vision. No additional seizure activity was observed in the emergency department.

Initial resuscitative measures included 2-large peripheral intravenous therapys, cardiac monitoring, pulse oximetry, normal saline infusion, and labs included: complete blood count, complete metabolic profile,prothrombin time/international normalized ratio, partial thromboplastin time, urine analysis with toxicology/drug screen, chest X-ray, electrocardiogram, CT brain with consults to obstetrics and neurology. Lab work revealed a mild leukocytosis; proteinuria 4+ and CT brain (Figure 1) demonstrated a left frontal subarachnoid hemorrhage with multiple hypodensities in the frontal and parieto-occipital subcortical white matter with significant vasogenic edema suggestive of PRES. Obstetrics recommended 4gi.v.magnesium sulfate that was initiated in the emergency department.

Figure 1. CT Brain without contrast (axial view).Left frontal subarachnoid hemorrhage (thin arrow) with subtle hypodensities in the cortex and subcortical white matter of both occipital lobes (bold arrows).

Neurology recommended ani.v.labetalol drip and magnetic resonance imaging/magnetic resonance angiography/magnetic resonance venography (Figure 2) to rule out venous thrombosis/aneurysm. Additional neurosurgical consult recommended serial CT scans to monitor subarachnoid hemorrhage.

Figure 2. MRI Flair (axial view).Left frontal subarachnoid hemorrhage (thin arrow) again is demonstrated, along with classic hyperintense white matter lesions of PRES in both occipital lobes (bold arrows).

The patient was admitted to the intensive care unit and further work-up was initiated that did not demonstrate any additional findings. The patient was subsequently discharged eight days later after a full recovery.

3. Discussion

Hincheyet al, first described PRES has having a unique neuroradiographical finding of vasogenic edema and clinical symptoms including headache, altered mental status, seizure and visual disturbances in 1996[1]. Vasogenic edema is the most predominant in the posterior portions of white matter[1,2]. Acute hypertensive encephalopathy is the well-known cause, along with fluid retention, immunosuppressive drugs and renal decompensation[1-3].

Interestingly, in pregnant and immediate post-partum women, pre-eclampsia (proteinuria and hypertension) and eclampsia (pre-eclampsia and seizure) are important causes of PRES[1,3]. The case described herein, the young female developed PRES in puerperium without any indicators of pre-eclampsia-eclampsia in her pregnancy[3,4]. Furthermore, intracranial hemorrhage has been also described in the setting of PRES, with a prevalence of 19.4%[2]. This case demonstrates a rare case of PRES with subarachnoid hemorrhage in a 25-yearold, post-partum female. Prompt emergency department diagnosis with appropriate and immediate consultations is paramount for optimum patient outcome.

Conflict of interest statement

The authors report no conflict of interest.

[1] Hinchey J, Chaves C, Appignani B, Breen J, Pao L, Wang A, et al. A reversible posterior leukoencephalopathy syndrome. N Engl J Med 1996; 334: 494-500.

[2] Sharma A, Whitesell RT, Moran KJ. Imaging pattern of intracranial hemorrhage in the setting of posterior reversible encephalopathy syndrome. Neuroradiology 2010; 52: 855-863.

[3] Uwatoko T, Toyoda K, Hirai Y, Shimada T, Yasumori K, Ibayashi S, et al. Reversible posterior leukoencephalopathy syndrome in a postpartum woman without eclampsia. Intern Med 2003; 42: 1139-1143.

[4] Vaughn CJ, Delanty N. Hypertensive emergencies. Lancet 2000; 356: 411-417.

ment heading

10.1016/S2221-6189(14)60054-8

*Corresponding author: Alexander J. Scumpia, D.O., M.Sc. Emergency Medicine Attending Physician, Department of Emergency Services, Memorial Regional Hospital 3501 Johnson Street Hollywood, FL 33021, U.S.A.

Tel: 1-917-371-3796

E-mail: ascumpia@yahoo.com

Leukoencephalopathy syndrome

Post-partum G2P2AO

Subarachnoid hemorrhage

主站蜘蛛池模板: 亚洲中文无码av永久伊人| 亚洲区第一页| 国产精品jizz在线观看软件| 国产黑丝视频在线观看| 99人妻碰碰碰久久久久禁片| 97久久超碰极品视觉盛宴| 国产sm重味一区二区三区| 久久久噜噜噜久久中文字幕色伊伊| 午夜福利免费视频| 91精品啪在线观看国产91| 中文字幕在线日韩91| 免费人成黄页在线观看国产| 色老头综合网| 71pao成人国产永久免费视频| 亚洲中文字幕久久精品无码一区| 99久久亚洲综合精品TS| 91精品国产综合久久香蕉922| 国产三级精品三级在线观看| 欧美中文字幕一区| 欧美自拍另类欧美综合图区| www.99精品视频在线播放| 精品1区2区3区| 色天堂无毒不卡| 理论片一区| 久久婷婷六月| 国产精品福利社| 国产日韩久久久久无码精品| 黄色三级毛片网站| 4虎影视国产在线观看精品| 亚洲精品va| 久久永久视频| 亚洲不卡影院| 国产在线精品人成导航| 国产精品福利一区二区久久| 久久精品波多野结衣| 亚洲床戏一区| 国产在线视频自拍| 亚洲AV无码乱码在线观看代蜜桃| 国产免费久久精品99re丫丫一| 欧美综合区自拍亚洲综合绿色| 国产精品青青| 九九热精品视频在线| 天天摸夜夜操| 亚洲视屏在线观看| 啪啪免费视频一区二区| 无码人妻热线精品视频| 欧美日韩亚洲国产主播第一区| 99国产精品国产| 亚洲av无码牛牛影视在线二区| 青青草国产一区二区三区| 亚洲高清资源| 国产成人精品2021欧美日韩| 中文精品久久久久国产网址| 日本高清有码人妻| 欧美成人午夜视频| 日韩第九页| 国产精品永久免费嫩草研究院| 中文成人在线| 人妻丰满熟妇αv无码| 国产午夜无码专区喷水| 欧美激情视频二区| 国产91色| 国产人成在线视频| 亚洲男人的天堂久久香蕉| 免费人成网站在线观看欧美| 538国产视频| 亚洲V日韩V无码一区二区| 毛片免费在线| www.av男人.com| 午夜日b视频| 91无码视频在线观看| 久草中文网| 国产精品页| 亚洲视频三级| 亚洲av日韩av制服丝袜| 亚洲欧美成人综合| 一区二区三区四区日韩| 亚洲欧美成人综合| 国产成人亚洲欧美激情| 老司国产精品视频| av一区二区人妻无码| 久久99国产视频|