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Long-term imaging course of Chiari malformation type I due to fibrous dysplasia/McCune-Albright syndrome.
Sato, Kei; Tsunoda, Keishi; Matsuo, Takayuki.
Afiliación
  • Sato K; Department of Neurosurgery, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki, 852-8501, Japan. satok.987@gmail.com.
  • Tsunoda K; Department of Neurosurgery, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki, 852-8501, Japan.
  • Matsuo T; Department of Neurosurgery, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki, 852-8501, Japan.
Childs Nerv Syst ; 38(9): 1817-1820, 2022 09.
Article en En | MEDLINE | ID: mdl-35790572
ABSTRACT

INTRODUCTION:

McCune-Albright syndrome (MAS) and fibrous dysplasia (FD) have been reported to cause Chiari type I malformation (CM1) and skull base invagination (BI). CASE A 6-year-old girl was diagnosed with MAS and FD. She was diagnosed with CM1 at age 8 years, and the syringomyelia had gradually increased by age 20 years. We performed foramen magnum decompression and C1 laminectomy, and the syringomyelia stopped spreading after surgery.

DISCUSSION:

This patient underwent long-term radiological observation and morphological evaluations, which revealed that the skull thickening was progressing, while the posterior cranial fossa volume (PCFV) remained unchanged for 14 years. Therefore, although PCFV did not decrease, it was considered to be relatively inadequate due to the increase in brain volume with growth, resulting in posterior fossa overcrowding, causing CM1.

CONCLUSION:

In patients with FD/MAS, long-term evaluation of bone thickening, odontoid position, and PCFV is necessary.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Malformación de Arnold-Chiari / Siringomielia / Displasia Fibrosa Poliostótica Límite: Adult / Child / Female / Humans Idioma: En Revista: Childs Nerv Syst Asunto de la revista: NEUROLOGIA / PEDIATRIA Año: 2022 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Malformación de Arnold-Chiari / Siringomielia / Displasia Fibrosa Poliostótica Límite: Adult / Child / Female / Humans Idioma: En Revista: Childs Nerv Syst Asunto de la revista: NEUROLOGIA / PEDIATRIA Año: 2022 Tipo del documento: Article País de afiliación: Japón