دولیکواکتازی ورتبروبازیلار: گزارش موردی
Authors
Abstract:
Background: Vertebrobasilar dolichoectasia is defined as a prominent elongation, dilatation and tortuosity of the vertebral and basilar arteries. Ectatic basilar arteries may cause different neurological symptoms by several mechanisms including compressive effects and embolic or ischemic events. Case presentation: In this report we present a 58-year old female patient who was admitted in Dr. Shariati General Hospital in Tehran, Iran with complaints of dysarthria, vertigo, ataxia and nausea. Neuro-imaging procedures (brain CT scan, CT angiography, and an MRI study of the blood vessels or MRA) were performed. Dilation and elongation, as well as tortuosity of the vertebral and basilar arteries revealed the diagnosis of vertebrobasilar dolichoectasia. The patient was discharged from the hospital following the control of underlying diseases and neurological symptoms related to dolichoectasia without undergoing any invasive procedures. Conclusion: Paying attention to any minor or major neurological symptoms, as well as underlying medical conditions along with the conservative control of symptoms can be most helpful. Invasive interventions in a chronically ill patient can be very risky, therefore, medical management including control of associated or underlying diseases is recommended as the first line of treatment.
similar resources
انسفالیت Bickerstaff: گزارش موردی
Background: Bickerstaff's brainstem encephalitis (BBE) is a very uncommon central nervous system disease with unknown etiology. As it is usually responsive to treatment, the diagnosis this disease is important. It seems There is no reported Bickerstaff's brainstem encephalitis case in Iran.Case presentation: An 83 year old woman presented with vertigo, ataxia and dysarthria from a week prior to...
full textگزارش موردی استئوژنزیس ایمپرفکتا
مقدمه و هدف: استئوژنزیس ایمپرفکتا یک اختلال ژنرالیزه بافت همبند است که اغلب به صورت اتوزومال غالب به ارث می رسد و خود را به صورت استخوان های شکننده و اسکلرای آبی و کاهش شنوایی نشان می دهد، در این گزارش به بررسی دو مورد بیمار مبتلا به استئوژنزیس ایمپرفکتا از یک خانواده پرداخته شده است. معرفی بیمار: بیمار اول آقای 18ساله ای است که به علت کاهش شنوایی دو طرفه در گوش سمت چپ (گوش مورد عمل) با40 د...
full textتومورال کلسینوزیس: گزارش موردی
Background: Tumoral calcinosis is a hereditary disorder of metabolic dysfunction of phosphate regulation. It is an idiopathic calcinosis that characterized by the deposition of calcium phosphate in periarticular tissues that causes typically lobulated, well demarcated calcification around large joints particularly the extensor surfaces. It is usually painless. It is common in puberty age and ad...
full textسیرنوملیا: یک گزارش موردی
در این مقاله یک مورد نوزاد مبتلا به سرنوملیا گزارش میشود. نوزاد مرده به دنیا آمد و اندامهای به هم متصل با آنومالیهای متعدد وجود داشت. به دلیل عدم انجام اتوپسی اطلاعات در مورد ناهنجاریهای داخلی در دسترس نمیباشد. با توجه به نیاز روزافزون مردم در خصوص آگاهیهای ژنتیکی ضروری است پرستاران به این منظور آموزش دیده تا بتوانند خدمت ارایه نمایند.
full textسندرم Gitelman: گزارش موردی
Background: Gitelman syndrome is a rare autosomal recessive disorder that typically presents with recurrent muscle cramps, carpopedal spasms, hypokalemic metabolic alkalosis, hypocalciuria and hypomagnesemia and high urine magnesium during adolescence. Mutation in the gene encoding for sodium chloride co-transporter in distal convoluted tubule causes electrolyte imbalance.Case presentation: We ...
full textدیسکراتوز مادرزادی: گزارش موردی
Background: Dyskeratosis Congenita (DC) is a rare inherited disease with an incidence of approximately one case per million population. The disease is characterized by a classic triad: nail changes, color reticulated skin and oral leukoplakia. In these patients, premature death is often associated with bone marrow failure, infections, pulmonary complications, or malignancy. Three patterns of in...
full textMy Resources
Journal title
volume 69 issue None
pages 327- 330
publication date 2011-08
By following a journal you will be notified via email when a new issue of this journal is published.
No Keywords
Hosted on Doprax cloud platform doprax.com
copyright © 2015-2023