Results 31 to 40 of about 3,496 (171)
Lumbosacral lipomyelomeningocele with anomalous osseous limb in a 3-month-old female
A patient with lipomyelomeningocele (known in utero) presented for MRI characterization prior to surgical procedure at three months of age. Cross-sectional imaging revealed a spinal dysraphism of the lower lumbar spine, with a posterior spinal defect ...
Sean L. Wilkes, MS, ALM +2 more
doaj +1 more source
Closed spinal dysraphism in a 6-month-old mixed breed dog
The term spinal dysraphism defines an incomplete fusion or a bone defect that affects the neural structures of the spinal cord due to a neural tube malformation.
Franco GG +8 more
doaj +1 more source
ABSTRACT A 7‐month‐old female presented with a congenital sacrococcygeal mass. While SCT and MMC are common, MRI ruled them out, leading to simple excision. Histopathology revealed a rare subcutaneous sacrococcygeal lipoma. This case emphasizes the use of advanced imaging to differentiate benign soft‐tissue lesions from spinal or neoplastic pathologies
Rajab Msemo +9 more
wiley +1 more source
Introduction Occult spinal dysraphism involves a wide range of congenital anomalies, e.g., lipoma, Lipomeningomyelocele, congenital dermal sinus, etc.
Ahmad Elsabaa +4 more
doaj +1 more source
ABSTRACT Currarino Syndrome (CS) should be suspected in infants presenting with persistent constipation and sacral anomalies. Early diagnosis using appropriate imaging and multidisciplinary surgical management is essential to prevent serious complications such as bowel obstruction, infection, and neurological impairment.
Ferdinand Medard Shilikale +4 more
wiley +1 more source
An Astonishing Extrarenal Wilms Localisation; Spinal Cord
Wilms’ tumour is a renal tumour mostly seen during the first 5 years of life and it accounts for 95% of renal malignancies during childhood. Its origin is primitive metanephric cells and, very rarely, it may occur in places other than the kidneys.
Ayşe Gülnur Tokuç +6 more
doaj +1 more source
ABSTRACT The simultaneous occurrence of Arnold–Chiari Malformation Type II (ACM II), syringomyelia, and an acquired tracheoesophageal fistula (TEF) in a young adult is exceptionally rare and represents a major diagnostic challenge. Arnold–Chiari Malformation II is characterized by the herniation of cerebellar structures through the foramen magnum.
Zahabia Adnan +6 more
wiley +1 more source
Spinal Dysraphism: Common Entity in Pediatric Neurosurgery
Introduction: Neural tube defects are among the most common congenital malformations and a major cause of health problems in surviving children, especially in developing countries.
Prakash Kafle +7 more
doaj +1 more source
MRI in Sheep Model for Myelomeningocele Repair Using a Novel Polymer and Other Dural Patches
ABSTRACT Objective To compare postnatal MRI outcomes after prenatal myelomeningocele repair using three different dural substitutes. Method 32 sheep fetuses were included, with 34.3%(11/32) serving as healthy controls and the remaining undergoing prenatal spinal lumbar defect creation to recreate a myelomeningocele in the fetus.
Usha D. Nagaraj +5 more
wiley +1 more source
Objective: To determine the diagnostic accuracy of ultrasonography in detecting spinal dysraphism in infants, taking MRI as the gold standard. Methodology: This cross-sectional study was conducted over a period of six months, from 30th May 2023 to ...
Nosheen Ahmad +5 more
doaj +1 more source

