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Updated Imaging Features of Dysplastic Cerebellar Gangliocytoma.
Dhamija, Radhika; Wood, Christopher P; Porter, Alyx B; Hu, Leland S; Weindling, Steven M; Hoxworth, Joseph M.
Afiliación
  • Wood CP; Division of Neuroradiology, Department of Radiology, Mayo Clinic, Rochester, MN.
  • Porter AB; Neurology, Mayo Clinic, Phoenix, AZ.
  • Hu LS; Division of Neuroradiology, Department of Radiology, Mayo Clinic, Phoenix, AZ.
  • Weindling SM; Division of Neuroradiology, Department of Radiology, Mayo Clinic, Jacksonville, FL.
  • Hoxworth JM; Division of Neuroradiology, Department of Radiology, Mayo Clinic, Phoenix, AZ.
J Comput Assist Tomogr ; 43(2): 277-281, 2019.
Article en En | MEDLINE | ID: mdl-30407243
ABSTRACT

OBJECTIVE:

The aim of this study was to perform an updated review of the imaging features of dysplastic cerebellar gangliocytoma (DCG).

METHODS:

Imaging findings were retrospectively reviewed in 14 patients with DCG. The analysis included size, location, cyst formation, calcification, intralesional hemorrhage, enhancement pattern, and apparent diffusion coefficient (ADC).

RESULTS:

In addition to revisiting many well-established imaging features of DCG, enhancement was much more common (64.3%) than previously reported, and small enhancing veins were also frequently encountered within or along the periphery of the lesions (50%). Dysplastic cerebellar gangliocytomas had an elevated ADC compared with normal cerebellum (967.8 ± 115.7 vs 770.4 ± 47.3 × 10 mm/s; P < 0.0001).

CONCLUSIONS:

Enhancement on magnetic resonance imaging within DCG should be an accepted imaging finding rather than being viewed as uncommon or atypical. Dysplastic cerebellar gangliocytomas typically have an elevated ADC compared with normal cerebellum, which may assist in differentiation from other posterior fossa neoplasms.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndrome de Hamartoma Múltiple / Imagen por Resonancia Magnética Tipo de estudio: Observational_studies Límite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Comput Assist Tomogr Año: 2019 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndrome de Hamartoma Múltiple / Imagen por Resonancia Magnética Tipo de estudio: Observational_studies Límite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Comput Assist Tomogr Año: 2019 Tipo del documento: Article