Anterior myelomeningocele manifesting as a posterior mediastinal mass has rarely been described. These anomalies, characterized by protrusion of meninges and spinal cord through open vertebral arches, manifest with devastating spinal or neurologic problems. This report describes the case of a young woman with a long-term history of right upper abdominal pain and low-grade fever but no associated neurologic or spinal defects. Relevant investigations showed a posterior mediastinal mass in the right paraspinal region. Through a right posterolateral thoracotomy, complete excision of the growth with preservation of major surrounding structures was performed. Histopathologic examination revealed myelomeningocele. This report discusses a rare case of anterior myelomeningocele at the thoracic level without neurospinal involvement.
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http://dx.doi.org/10.1016/j.athoracsur.2019.06.105 | DOI Listing |
Int J Gynaecol Obstet
December 2024
Al-Hadi Laboratory and Medical Center, Beirut, Lebanon.
Br J Neurosurg
November 2024
CHU de Poitiers, Service de Neurochirurgie du rachis, Chirurgie de la Douleur et du Handicap, France.
Case Report: A rare case of Klippel-Feil syndrome associated with anterior cervical meningomyelocele is reported, treated successfully using partial cervical corpectomy, spinal cord microsurgical reinsertion into the spinal canal, and vertebral reconstruction. A 71-year-old patient presented with upper limb paraesthesia, chronic neck pain, and progressive motor distal impairment. Cervical spine imaging revealed an anterior cervical meningomyelocele digging into C7 vertebra and underlying adjacent congenital fusion blocks.
View Article and Find Full Text PDFNeuropsychology
November 2024
Department of Psychology, University of Houston.
J Cancer Res Ther
April 2024
Department of Pediatric Surgery, All India Institute of Medical Sciences, Bhubaneswar, Odisha, India.
Currarino syndrome (CS) is a rare congenital syndrome characterized by a triad of anorectal malformation, sacral deformity, and presacral mass. In about 50% of cases, it is caused by HLXB9 gene mutation in chromosome 7q36. A 13-month-male child presented with presacral discharging sinus with a history of surgery for anorectal malformation and perineal fistula at the time of birth.
View Article and Find Full Text PDFGait Posture
September 2024
Department of Women's and Children's Health, Karolinska Institutet, Karolinska vägen 37 A, Q2:07, Stockholm 171 76, Sweden.
Background: Individuals with myelomeningocele (MMC) present with neurological and orthopaedic deficiencies, requiring orthoses during walking. Orthoses for counteracting dorsiflexion may restrict activities such as rising from a chair.
Research Question: How are sit-to-stand (STS) movements performed with ankle joint-restricted ankle-foot orthoses (AFO) and knee-ankle-foot orthoses with a free-articulated knee joint (KAFO-F)?
Methods: Twenty-eight adults with MMC, mean age 25.
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