Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters










Database
Language
Publication year range
1.
Sud Med Ekspert ; 67(1): 10-13, 2024.
Article in Russian | MEDLINE | ID: mdl-38353008

ABSTRACT

OBJECTIVE: To study morphological changes of cerebral cortex in young people under the conditions of chronic alcohol intoxication (CAI). MATERIAL AND METHODS: Morphometric examination of cerebral cortex fragments obtained from 28 persons who died with a CAI diagnosis (average age was 38 years), and 25 subjects who died from other causes, which are not associated with alcohol consumption (average age was 39 years), was carried out. RESULTS: It was shown that neurons of pathological shapes, including hypo- and hyperchromic, pyknotic and «shadow-like¼, were dominant in group of CAI. There was an increase in the glial index and a greater intensity of perivascular and pericellular edema compared to the control group. CONCLUSION: Morphological changes of cerebral cortex under the conditions of CAI are non-specific and largely similar to neurodegenerative alterations in other pathological conditions, senile dementia. Clearer histological criteria for alcoholic encephalopathy are needed, including with the use of immunohistochemical methods.


Subject(s)
Alcoholic Intoxication , Alcoholism , Humans , Adolescent , Adult , Alcoholic Intoxication/pathology , Alcoholism/complications , Alcoholism/pathology , Cerebral Cortex/pathology , Neurons/pathology , Death
2.
Arkh Patol ; 86(1): 49-51, 2024.
Article in Russian | MEDLINE | ID: mdl-38319272

ABSTRACT

A rare clinical case of a newborn boy with a diagnosed Potter sequence is presented. The diagnosis was made based on polycystic dysplasia of the kidneys, cysts in the liver, hypoplasia of the lungs and characteristic external signs due to critical oligohydramnios. The child's parents were closely related, which suggested an autosomal recessive form of the disease. The newborn lived for 15 hours, after which the death, developed as a result of respiratory failure, was ascertained.


Subject(s)
Polycystic Kidney Diseases , Male , Child , Infant, Newborn , Female , Pregnancy , Humans , Polycystic Kidney Diseases/diagnosis , Polycystic Kidney Diseases/genetics , Kidney , Hyperplasia , Liver
SELECTION OF CITATIONS
SEARCH DETAIL
...