Late adult onset of Langerhans cell histiocytosis mimicking glioblastoma multiforme

Autor: Thierry Rochat, Fabienne Perren, B. Thiévent, Jean-Claude Pache, Theodor Landis, Jacqueline Delavelle, Carlo Chizzolini, L. Fankhauser
Jazyk: angličtina
Rok vydání: 2011
Předmět:
Pathology
Internal capsule
Biopsy
ddc:616.07
Dexamethasone
Mycophenolic Acid/administration & dosage/analogs & derivatives/therapeutic use
030218 nuclear medicine & medical imaging
0302 clinical medicine
Langerhans cell histiocytosis
Age of Onset
Dexamethasone/administration & dosage/therapeutic use
Paresis/etiology
Lung
Bone and Bones/pathology
ddc:616
Brain Diseases
medicine.diagnostic_test
Brain Neoplasms
Brain
Middle Aged
Cerebellar Ataxia/etiology
Magnetic Resonance Imaging
3. Good health
Paresis
medicine.anatomical_structure
Neurology
Alien Limb Phenomenon
Drug Therapy
Combination

Female
Brain Diseases/complications/diagnosis/drug therapy
medicine.medical_specialty
Multiple Sclerosis
Cerebellar Ataxia
Central nervous system
Lung/pathology
Histiocytosis
Langerhans-Cell/complications/diagnosis/drug therapy/epidemiology

Bone and Bones
Central nervous system disease
Diagnosis
Differential

03 medical and health sciences
Alien Hand Syndrome/etiology
medicine
Humans
Brain/pathology
Glioblastoma/diagnosis
Brain Neoplasms/diagnosis
business.industry
Brain biopsy
Multiple sclerosis
Mycophenolic Acid
medicine.disease
ddc:616.8
Histiocytosis
Langerhans-Cell

Neurology (clinical)
Multiple Sclerosis/diagnosis
business
Glioblastoma
030217 neurology & neurosurgery
Zdroj: Journal of the Neurological Sciences, Vol. 301, No 1-2 (2011) pp. 96-9
Journal of the neurological sciences
ISSN: 0022-510X
Popis: Langerhans cell histiocytosis (LCH) with multiple organ involvement is a rare disorder in adults. Extrapituitary involvement of the central nervous system (CNS) is uncommon. We report the unusual case of a 55-year-old woman presenting with a left-sided hemiataxia-hemiparesis, left hemisensory loss and short-lasting episodes of an alien left hand due to lesions of the internal capsule and the right thalamus, extending into the mesencephalon associated with extensive surrounding edema, without pituitary involvement. The neuroradiological image suggested glioblastoma multiforme. Brain biopsy revealed inflammatory tissue and "pseudotumoral" multiple sclerosis was suspected. Biopsy of concomitant lung and bone lesions disclosed Langerhans cell histiocytosis. The treatment with pulsed steroids in association with mycophenolate mofetil led to a sustained, clinical neurological remission.
Databáze: OpenAIRE