Publications by authors named "Pavani Adapa"

Purpose: Perfusion and diffusion magnetic resonance imaging (MRI) provide important biomarkers for brain tumor analysis. Our aim was to investigate if regions of increased perfusion or tumor with restricted diffusion on the immediate post-operative MRI examination would be predictive of time to tumor progression in patients with high-grade gliomas.

Materials And Methods: Twenty-three patients with high-grade gliomas were retrospectively analyzed.

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Article Synopsis
  • This study focuses on using high-resolution MRI techniques to better understand the human visual system through a method called diffusion tensor fiber tractography (DTT).
  • It involved five healthy male participants, aged 24-37, who provided data after the university's ethics approval.
  • The researchers successfully reconstructed and quantified critical components of the visual pathways, such as the optic chiasm and optic tracts, using a specialized imaging protocol that minimized interference from other brain structures.
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Aim: Angelman syndrome is a neurogenetic disorder characterized by severe intellectual disability, absent speech, seizures, and outbursts of laughter. The aim of this study was to utilize diffusion tensor imaging (DTI) to examine alterations in white matter pathways in Angelman syndrome, with an emphasis on correlations with clinical severity.

Method: DTI was used to examine the arcuate fasciculus (AF), uncinate fasciculus (UF), inferior longitudinal fasciculus (ILF), inferior fronto-occipital fasciculus (IFOF), and the corpus callosum (CC).

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Precalcaneal soft-tissue lesions are uncommon in the pediatric population and can present a diagnostic challenge. Fibrous hamartoma of infancy (FHI) is relatively rare in this location. We report an interesting case of FHI in a 3-years-and-10-months-old boy in the precalcaneal location that was present since birth.

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Ewing sarcoma of the bone is a highly malignant round-cell tumor that typically presents between 10 to 20 years of age and is more common in boys. It can have an extraosseous origin, although it is rare. We report a case of extraosseous Ewing sarcoma in the thyroid gland in a 9-year-old girl.

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