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Nondysraphic intramedullary spinal cord lipoma: a case report.
Karki, Susmin; Regmi, Prakash; Parajuli, Asmita; Kumari, Khusbu; Thapa, Bikas; Shilpakar, Sushil K.
Afiliação
  • Karki S; Maharajgunj Medical Campus.
  • Regmi P; Department of Neurosurgery, Tribhuvan University Institute of Medicine, Maharajgunj, Nepal.
  • Parajuli A; Maharajgunj Medical Campus.
  • Kumari K; Maharajgunj Medical Campus.
  • Thapa B; Department of Neurosurgery, Tribhuvan University Institute of Medicine, Maharajgunj, Nepal.
  • Shilpakar SK; Department of Neurosurgery, Tribhuvan University Institute of Medicine, Maharajgunj, Nepal.
Ann Med Surg (Lond) ; 86(6): 3683-3689, 2024 Jun.
Article em En | MEDLINE | ID: mdl-38846861
ABSTRACT

Introduction:

Intramedullary nondysraphic spinal lipomas are extremely rare among primary spinal cord tumors. These patients present with nonspecific sensory symptoms followed by deterioration of motor symptoms. As the safety margins for neurological preservation are thin, meticulously locating the extent of the tumor and choosing the resection modalities is essential. Case report The authors report a rare case of a 35-year-old male who presented with progressive difficulty in walking for 6 months associated with numbness and tingling sensation in the bilateral upper and lower limbs. He was diagnosed with nondysraphic intramedullary cervicothoracic lipoma and underwent subtotal resection of the tumor.

Conclusion:

Nondysraphic intramedullary spinal cord lipomas are rare and may present as nonspecific neurological symptoms. Hence, they should be considered differentials of intramedullary spinal cord tumors. Surgery appears to be the mainstay of treatment.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article