CASE REPORT OF AORTITIS SYNDROME IN WHICH REVASCULIZATION PREVENTED BLINDNESS

نویسندگان
چکیده

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Bilateral cortical blindness--Anton syndrome: case report.

The aim of this work is the specify of rare neurological disorder, bilateral cortical blindness and Anton syndrome. It is about loss of vision in the presence of intact anterior pathways and a form of visual anosognosia, with resulting patient denial of blindness. This is a case of 72-year old man with history of diabetes and hypertension. Diagnosis is based on the exclusion of disease in the a...

متن کامل

IgG4 Aortitis: A Case Report.

IgG4 aortitis is one of the entities seen in the spectrum of IgG4-related disease (IgG4-RD). It is characterized by serologic (elevated serum IgG4) and histologic features including a lymphoplasmacytic infiltrate with increased numbers of IgG4-positive plasma cells, storiform fibrosis and obliterative phlebitis. Some studies have described a correlation between infections and IgG4 aortitis. We ...

متن کامل

Infectious Thoracic Aortitis: A Case Report

Aortitis is a term that refers to infectious or noninfectious conditions in which there is abnormal inflammation of the aortic wall. Here we report the case of a 32 years old woman who presented a diabetic Ketoacidosis. The thoraco abdominal CT scan showed endoluminal defect of the thoracic aorta with splenic and reanl infarction. Transesophageal echocardiogram showed a normal aortic and mitral...

متن کامل

Psychological Blindness - a Case Report

Rarely does malingering present in the form of complete blindness and that too of prolonged duration, in presence of possible organic corroboration and well supported by relatives. This case is reported to highlight the extremes of psychological production of symptoms and how it can be successfully dealt with.

متن کامل

Report of a Case Report of Kindler Syndrome

A 13 years old boy with progressive poikiloderma, bullous lesions in the extremities and photosensitivity is reported. Physical examinations were otherwise normal, his physical development was normal, no other family member had a similar disease. Routin laboratory exams were in the normal limits.Histopathology exams from poikilodermatous skin showed atrophy of the epidermis, liquification degen...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: The journal of the Japanese Practical Surgeon Society

سال: 1987

ISSN: 0386-9776

DOI: 10.3919/ringe1963.48.54