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Association of limited dorsal myeloschizis and corpus callosum lipoma: A case report and literature review.
El Marrakchi, Malak; Zian, Nahla; Hajhouji, Farouk; Laghmari, Mehdi; Ghannane, Houssine; Jallo, George; Benali, Said Ait.
Affiliation
  • El Marrakchi M; Department of Neurosurgery, Mohammed VI University Hospital Center of Marrakesh, Cadi Ayyad University, Faculty of Medicine, Marrakesh, Morocco.
  • Zian N; Department of Neurosurgery, Mohammed VI University Hospital Center of Marrakesh, Cadi Ayyad University, Faculty of Medicine, Marrakesh, Morocco.
  • Hajhouji F; Department of Neurosurgery, Mohammed VI University Hospital Center of Marrakesh, Cadi Ayyad University, Faculty of Medicine, Marrakesh, Morocco.
  • Laghmari M; Department of Neurosurgery, Mohammed VI University Hospital Center of Marrakesh, Cadi Ayyad University, Faculty of Medicine, Marrakesh, Morocco.
  • Ghannane H; Department of Neurosurgery, Mohammed VI University Hospital Center of Marrakesh, Cadi Ayyad University, Faculty of Medicine, Marrakesh, Morocco.
  • Jallo G; Department of Pediatric Neurosurgery, Institute for Brain Protection Sciences, Johns Hopkins All Children's Hospital, St. Petersburg, Florida, United States.
  • Benali SA; Department of Neurosurgery, Mohammed VI University Hospital Center of Marrakesh, Cadi Ayyad University, Faculty of Medicine, Marrakesh, Morocco.
Surg Neurol Int ; 15: 151, 2024.
Article in En | MEDLINE | ID: mdl-38741980
ABSTRACT

Background:

Intracranial lipomas are a rare clinical entity. These lesions are frequently asymptomatic and originate in the pericallosal area. As they are fat-containing lesions which are intimately attached to the surrounding structures, surgery is not recommended. In some individual reports, subtotal resection is recommended to lessen complications. There have been no previous reports of corpus callosum lipoma (CCL) associated with limited dorsal myeloschizis (LDM). Case Description We describe the case of a combination of CCL and bilateral choroid plexus lipoma discovered incidentally during the investigation of LDM in a 3-month-old male child. Given the asymptomatic behavior of the lipoma and the vascular elements of the pericallosal area, it was decided to monitor it regularly. Thus, the patient underwent surgery only for LDM. Histological examination confirmed the diagnosis, and postoperative follow-up 1 year after showed good evolution. To the best of our knowledge, this association has never been described in the literature.

Conclusion:

This case suggests a possible developmental relationship between CCL and spinal dysraphism.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Surg Neurol Int Year: 2024 Document type: Article Affiliation country: Morocco

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Surg Neurol Int Year: 2024 Document type: Article Affiliation country: Morocco
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