lenticulostriate vasculopathy
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Children ◽  
2021 ◽  
Vol 8 (12) ◽  
pp. 1166
Author(s):  
Yi-Li Hung ◽  
Chung-Min Shen ◽  
Kun-Long Hung ◽  
Wu-Shiun Hsieh

Background: The pathogenesis and clinical significance of lenticulostriate vasculopathy (LSV) are unclear. Our study aimed to determine the prevalence, presentation, and evolution of LSV, and the perinatal risk factors associated with LSV among very-low-birth-weight (VLBW) preterm infants. Methods: One-hundred-and-thirty VLBW preterm infants were retrospectively enrolled in this study. Serial cranial ultrasound examinations were performed regularly from birth until a corrected age of 1 year. Infants with LSV were assigned to early-onset (≤10 postnatal days) and late-onset (>10 postnatal days) groups. Data describing the infants’ perinatal characteristics, placental histopathology, and neonatal morbidities were collected, and the groups were compared. Results: Of the VLBW infants, 39.2% had LSV before they were 1 year old. Linear-type LSV was the most common presentation, and >50% of the infants had bilateral involvement. LSV was first detected at 112 ± 83 postnatal days, and its detection timing correlated negatively with gestational age (GA) (R2 = 0.153, p = 0.005) and persisted for 6 months on average. The infants with and without LSV had similar perinatal characteristics, placental pathologies, cytomegalovirus infection rates, and clinical morbidities. The late-onset LSV group comprised 45 (88.2%) infants who had a significantly higher rate of being small for gestational age (SGA) and used oxygen for longer than the infants without LSV. After adjusting a multivariable regression model for GA and SGA, analysis showed that the duration of oxygen usage was an independent risk factor for late-onset LSV development in VLBW infants (odds ratio: 1.030, p = 0.032). Conclusion: LSV may be a nonspecific marker of perinatal insult to the developing brains of preterm infants. Prolonged postnatal oxygen usage may predispose VLBW preterm infants to late-onset LSV development. The long-term clinical impacts of LSV should be clarified.


Author(s):  
Jamie Strause ◽  
Kofi-Buaku Atsina ◽  
Darren Bialo ◽  
Jonathan Orwitz ◽  
Ronald L. Wolf ◽  
...  

2018 ◽  
Vol 38 (10) ◽  
pp. 1370-1378 ◽  
Author(s):  
Julide Sisman ◽  
Lina Chalak ◽  
Roy Heyne ◽  
Marcia Pritchard ◽  
Devri Weakley ◽  
...  

2018 ◽  
Vol 33 (2) ◽  
pp. 146-152 ◽  
Author(s):  
Jatinder Singh Goraya ◽  
Shivankshi Berry ◽  
Kavita Saggar ◽  
Archana Ahluwalia

The authors retrospectively reviewed charts of the children with basal ganglia stroke who either had preceding minor head injury or showed basal ganglia calcification on computed tomography (CT) scan. Twenty children, 14 boys and 6 girls were identified. Eighteen were aged between 7 months to 17 months. Presentation was with hemiparesis in 17 and seizures in 3. Preceding minor head trauma was noted in 18. Family history was positive in 1 case. Bilateral basal ganglia calcification on CT scan was noted in 18. Brain magnetic resonance imaging done in 18 infants showed acute or chronic infarcts in basal ganglia. Results of other laboratory and radiological investigations were normal. Four infants were lost to follow-up, 9 achieved complete or nearly completely recovery, and 7 had persistent neurological deficits. Basal ganglia calcification likely represents mineralized lenticulostriate arteries, a marker of lenticulostriate vasculopathy. Abnormal lenticulostriate vessels are vulnerable to injury and thrombosis after minor head trauma resulting in stroke.


2017 ◽  
Author(s):  
Henry Knipe ◽  
Francis Fortin

Author(s):  
Beata Acs ◽  
Lucica Ghiţ&acaron; ◽  
Vasilica Pl&acaron;iaşu ◽  
Ionela Voicil&acaron; ◽  
Iuliana Balint-Boia ◽  
...  

2017 ◽  
Vol 34 (08) ◽  
pp. 780-786 ◽  
Author(s):  
Abby Robinson ◽  
John Flibotte ◽  
Summer Kaplan ◽  
Sara DeMauro

Objective The objective of this study was to perform a systematic review of all studies that report neurodevelopmental outcomes at 12 months' corrected age or later for preterm infants (< 32 weeks) who are diagnosed with lenticulostriate vasculopathy (LSV) on cranial ultrasound. Study Design This is a systematic review. Results We identified 501 unique publications of which 3 met all prespecified eligibility criteria. Neurodevelopmental outcome data were available for 44 preterm infants with LSV. There were mixed results from the studies: the first reported impairments of mental development; the second reported impairments of motor development only; and finally, the third reported that three of three preterm infants with LSV had mild or moderate developmental delay. Conclusion The available results raise some concern for future impairments in preterm infants with LSV, but they are conflicting and inconclusive. There is insufficient evidence about the neurodevelopmental implications of LSV in preterm infants to inform counseling of parents.


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