"Encephalomalacia" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Softening or loss of brain tissue following CEREBRAL INFARCTION; cerebral ischemia (see BRAIN ISCHEMIA), infection, CRANIOCEREBRAL TRAUMA, or other injury. The term is often used during gross pathologic inspection to describe blurred cortical margins and decreased consistency of brain tissue following infarction. Multicystic encephalomalacia refers to the formation of multiple cystic cavities of various sizes in the cerebral cortex of neonates and infants following injury, most notably perinatal hypoxia-ischemic events. (From Davis et al., Textbook of Neuropathology, 2nd ed, p665; J Neuropathol Exp Neurol, 1995 Mar;54(2):268-75)
| Descriptor ID |
D004678
|
| MeSH Number(s) |
C10.228.140.461
|
| Concept/Terms |
Multicystic Encephalomalacia- Multicystic Encephalomalacia
- Encephalomalacias, Multicystic
- Multicystic Encephalomalacias
- Encephalomalacia, Multicystic
|
Below are MeSH descriptors whose meaning is more general than "Encephalomalacia".
Below are MeSH descriptors whose meaning is more specific than "Encephalomalacia".
This graph shows the total number of publications written about "Encephalomalacia" by people in this website by year, and whether "Encephalomalacia" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2000 | 0 | 1 | 1 |
| 2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "Encephalomalacia" by people in Profiles.
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Paenibacillus dendritiformis Meningitis, Brain Abscesses and Cystic Encephalomalacia in an Infant: Case Presentation and Review of the Literature. Pediatr Infect Dis J. 2022 12 01; 41(12):e544-e547.
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Long-term outcome in twin-twin transfusion syndrome treated with serial aggressive amnioreduction. Am J Obstet Gynecol. 2000 Jul; 183(1):211-7.
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Neuropathologic findings in cortical resections (including hemispherectomies) performed for the treatment of intractable childhood epilepsy. Acta Neuropathol. 1992; 83(3):246-59.
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An autosomal dominant form of necrotizing encephalomyelopathy resembling a spinocerebellar degeneration. Trans Am Neurol Assoc. 1975; 100:47-51.