نتایج جستجو برای: malformation

تعداد نتایج: 15277  

Journal: :iranian journal of neurology 0
alireza khoshnevisan department of neurosurgery, shariati hospital, tehran university of medical sciences, tehran, iran. askar ghorbani department of neurology, shariati hospital, tehran university of medical sciences, tehran, iran. narges sistany allahabadi student of medicine, school of medicine, tehran university of medical sciences, tehran, iran. farshid farzaneh department of neurosurgery, shariati hospital, tehran university of medical sciences, tehran, iran. sina abdollahzadeh department of neurosurgery, shariati hospital, tehran university of medical sciences, tehran, iran. sepehr soleymani student of medicine, school of medicine, tehran university of medical sciences, tehran, iran.

central nervous system infection is a rare complication of endovascular procedures. we report a 21-year-old woman presented with headache, nausea, vomiting, and right-sided hemiparesis 4 months after endovascular embolization of cerebral arteriovenous malformation. investigations led to the diagnosis of multiple brain abscesses. this is the sixth case report of brain abscess following endovascu...

Journal: :iranian journal of allergy, asthma and immunology 0
soheila aleyacin mozhgan moghtaderi reza amin sayyed yahya attaran

hyper - immunoglobulin e syndrome is a rare primary immunodeficiency disease characterized by recurrent abscess formation, respiratory tract infections and very high titers of serum ige associated with peculiar face and skeletal features. we report a seven-year old  girl  presenting with persistent productive cough and  history of chronic eczematoid facial lesions since infancy  and  two episod...

Journal: : 2021

Dandy-Walker malformation is a rare congenital malformation, characterized by agenesis or hypoplasia of the cerebellar vermis, cystic dilatation 4th ventricle and enlargement posterior fossa. Postnatal hydrocephalus develops in approximately 70-90% patients. The relationship with postaxial polydactyl has been defined as possible autosomal recessive syndrome (OMIM 220220). Here, we present an in...

Congenital cystic Adenomatoid malformation is a rare developmental abnormality of the lung occuring in 1-4/100000 live births.In most cases the outcome with CCAM in fetus is very good,while in some cases the outcome is very bad and can be life threatning for the fetus.we report here a case of 40 day old female infant who presented with worsening respiratory distress since birth and x ray and CT...

Journal: :Annals of hepatology 2017
Hui Li Zhi Ma Ying Xie Feng Tian

The Abernethy malformation is a rare congenital malformation defined by the presence of an extrahepatic portosystemic shunt. Although most patients are asymptomatic, clinical encephalopathy is present in 15% of cases. We present a patient with type 2 Abernethy malformation, hyperammonemia, and encephalopathy. Shunt closure was performed successfully using interventional angiography; however, hy...

Journal: :The Saudi dental journal 2011
Ravi Prakash S Mohan Manu Dhillon Navneet Gill

The most common type of vascular malformation is the venous malformation and these are occasionally associated with phleboliths. We report a case of a 45 year old woman with intraoral venous malformation with phleboliths.

2016
Reid A. Maclellan Gulraiz Chaudry Arin K. Greene

UNLABELLED Primary lymphedema and capillary malformation are independent vascular malformations that can cause overgrowth of the lower extremity. We report a series of patients who had both types of malformations affecting the same leg. The condition is unique but may be confused with other types of vascular malformation overgrowth conditions (eg, Klippel-Trenaunay and Parkes Weber). METHODS ...

Journal: :Dermato 2021

Klippel-Trenaunay syndrome (KTS) is a rare complex vascular with limb hypertrophy. KTS diagnosed if at least two of the three features capillary malformation, venous and soft tissue and/or bone overgrowth are present. Of these, malformation (i.e., port-wine stain) most commonly observed feature but may be absent in atypical KTS. We herein report case unilateral

Journal: :Thorax 1999
M Samuel D M Burge

BACKGROUND Sequestration with associated cystic adenomatoid malformation is rare. A study was undertaken to determine whether pulmonary sequestration associated with congenital cystic adenomatoid malformation has a more favourable natural history than that of sequestration without associated cystic adenomatoid malformation. METHODS An outline of the postnatal work up leading to the management...

2016
Guang-Han Wang Lan Zhu Ai-Ming Liu Tao Xu Jing-He Lang

BACKGROUND Female genital malformations represent miscellaneous deviations from normal anatomy. This study aimed to explore the clinical characteristics of patients who underwent surgery for genital tract malformations at Peking Union Medical College Hospital (PUMCH) during a 31-year period. METHODS We retrospectively reviewed surgical cases of congenital malformation of the female genital tr...

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