RSS-Feed abonnieren
Bitte kopieren Sie die angezeigte URL und fügen sie dann in Ihren RSS-Reader ein.
https://www.thieme-connect.de/rss/thieme/de/10.1055-s-00034924.xml
Nuklearmedizin 2019; 58(05): 403-404
DOI: 10.1055/a-0972-0698
DOI: 10.1055/a-0972-0698
Case Report
Diagnosis of Huntington’s disease via sequential 18F-DOPA and 18F-FDG PET/MRI
Erstdiagnose eines Morbus Huntington mittels 18F-DOPA und 18F-FDG PET/MRIWeitere Informationen
Publikationsverlauf
Publikationsdatum:
25. Juli 2019 (online)

Introduction
Cases of rare movement disorders like Huntington’s disease (HD) are not easy to diagnose, especially when occurring sporadically, without documented family history. In HD patients, MRI scans commonly feature atrophy of the striatum and reduced volume of white matter. But if morphological findings remain unspecific, functional PET imaging could provide valuable information to further clarify diagnosis. We present a case report of a 56-year-old woman suffering from mild hypokinetic-rigid syndrome and depression, suspicious of Parkinson’s disease, who was referred to 18F-DOPA and 18F-FDG PET/MRI scans at our department.
-
References
- 1 Ibrahim N, Kusmirek J, Struck AF, Floberg JM, Perlman SB, Gallagher C. et al. The sensitivity and specificity of F-DOPA PET in a movement disorder clinic. Am J Nucl Med Mol Imaging 2016; 6 (01) 102-109
- 2 Minkova L., Gregory S., Scahill I. R., Abdulkadir A., Kaller P. C.. et al. Cross-sectional and longitudinal voxel-based grey matter asymmetries in Huntington’s disease. NeuroImage: Clin 2018; 17: 312-324
- 3 Lizarraga KJ, Gorgulho A, Chen W, De Salles AA. Molecular imaging of movement disorders. World J Radiol 2016; 8: 226-39
- 4 López-Mora DA, Camacho V, Pérez-Pérez J, Martínez-Horta S, Fernández A, Sampedro F. et al. Striatal hypometabolism in premanifest and manifest Huntington’s disease patients. Eur J Nucl Med Mol Imaging 2016; 43: 2183-2189
- 5 Langbehn DR, Brinkman RR, Falush D, Paulsen JS, Hayden MR. A new model for prediction of the age of onset and penetrance for Huntington’s disease based on CAG length. Clin Genet 2004; 65: 267-277
- 6 Furukawa F, Ishikawa K, Yokota T, Sanjo N. Cross-Sectional Area Analysis of the Head of the Caudate Nucleus in Huntington’s Disease. Eur Neurol 2019; 81: 13-18