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1.
Angiol Sosud Khir ; 26(2): 170-174, 2020.
Article in Russian | MEDLINE | ID: mdl-32597899

ABSTRACT

Gastrointestinal haemorrhage is a common cause of emergency admission of patients to surgical hospitals. Within the structure of nosological entities, not unreasonably referred to the rarest causes of gastrointestinal bleeding is the formation of an aortointestinal fistula whose early diagnosis is of paramount importance. The clinical picture may be different but it is mostly represented by gastrointestinal haemorrhage. The incidence of gastrointestinal fistulas following a surgical intervention ranges from 0.6 to 2.3%. Unless timely diagnosed and with incorrect therapeutic decision-making, the mortality rate amounts to 90%. In this article we present a clinical case report regarding successful treatment of a patient presenting with a secondary aortoduodenal fistula occurring 5 years after previously performed aortofemoral bypass grafting and complicated by relapsing intestinal bleeding and acute ischaemia of the right lower extremity.


Subject(s)
Aortic Diseases/diagnosis , Duodenal Diseases/diagnosis , Duodenal Diseases/etiology , Duodenal Diseases/surgery , Intestinal Fistula/diagnosis , Intestinal Fistula/etiology , Intestinal Fistula/surgery , Aorta, Abdominal , Gastrointestinal Hemorrhage/diagnosis , Humans
2.
Vestn Ross Akad Med Nauk ; (9-10): 11-8, 2006.
Article in Russian | MEDLINE | ID: mdl-17111918

ABSTRACT

The article is dedicated to the problems of intellectual disorders in children suffering from congenital and hereditary diseases, and reflects the issues of the medicosocial significance of neuropsychical impairment in children and the proportion of ethiological factors in the genesis of mental retardation. The authors consider modern diagnostic and preventive technologies that are used in pediatric practice in children with hereditary and congenital intellectual developmental disorders.


Subject(s)
Intellectual Disability , Adult , Brain Mapping , Child , Child, Preschool , Chromosome Aberrations , Clinical Enzyme Tests , Counseling , Down Syndrome/diagnosis , Down Syndrome/genetics , Electroencephalography , Female , Humans , Infant , Infant, Newborn , Intellectual Disability/diagnosis , Intellectual Disability/etiology , Intellectual Disability/genetics , Intellectual Disability/prevention & control , Male , Neonatal Screening , Psychological Tests , Risk Factors
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