MRI features of intra-axial histiocytic brain mass lesions.


Journal

Clinical radiology
ISSN: 1365-229X
Titre abrégé: Clin Radiol
Pays: England
ID NLM: 1306016

Informations de publication

Date de publication:
Feb 2021
Historique:
received: 11 02 2020
accepted: 15 09 2020
pubmed: 21 10 2020
medline: 29 6 2021
entrez: 20 10 2020
Statut: ppublish

Résumé

To describe MRI features, including diffusion-weighted imaging (DWI), magnetic resonance spectroscopy (MRS), and perfusion-weighted imaging (PWI), of intra-axial tumour-like presentations of four different subtypes of histiocytosis. The brain MRI findings of 23 patients with histologically proven histiocytosis were reviewed retrospectively (11 Langerhans cell histiocytosis [LCH], eight Erdheim-Chester disease [ECD], one overlap form LCH/ECD, two Rosai-Dorfman disease [RDD], and one haemophagocytic lymphohistiocytosis [HLH]) with single or multiple enhancing intraparenchymal brain lesions. Histiocytic brain mass lesions show some similar MRI features including Supra and/or infratentorial and/or paraventricular subcortical well-delineated masses, linear ependymal enhancement along the ventricles and brain stem lesions. Masses always present with mixed hyper- and hypointense signal on T2-weighted imaging (WI). Their enhancement is often homogeneous. Apparent diffusion coefficient (ADC) values are often normal or elevated. The presence of multiple periventricular and subcortical enhancing lesions with mixed signal intensity on T2WI and normal or high ADC values should lead radiologists to consider the diagnosis of histiocytic lesions and search for associated systemic lesions.

Identifiants

pubmed: 33077156
pii: S0009-9260(20)30425-6
doi: 10.1016/j.crad.2020.09.015
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

159.e19-159.e28

Informations de copyright

Copyright © 2020 The Royal College of Radiologists. Published by Elsevier Ltd. All rights reserved.

Auteurs

L P Luna (LP)

Russell H. Morgan Department of Radiology and Radiological Science, Division of Neuroradiology, The Johns Hopkins University School of Medicine, Baltimore, USA. Electronic address: lluna6@jhmi.edu.

A Drier (A)

APHP, Department of Neuroradiology, Pitié-Salpêtrière Hospital, Paris, France.

N Aygun (N)

Russell H. Morgan Department of Radiology and Radiological Science, Division of Neuroradiology, The Johns Hopkins University School of Medicine, Baltimore, USA.

K Mokhtari (K)

APHP, Department of Neuropathology, Pitié-Salpêtrière Hospital, Paris, France.

K Hoang-Xuan (K)

APHP, Department of Neuro-oncology, Pitié-Salpêtrière Hospital, Paris, France.

D Galanaud (D)

APHP, Department of Neuroradiology, Pitié-Salpêtrière Hospital, Paris, France.

J Donadieu (J)

APHP, Department of Hematology, Trousseau Hospital, Paris, France.

D Dormont (D)

APHP, Department of Neuroradiology, Pitié-Salpêtrière Hospital, Paris, France.

J Haroche (J)

APHP, Department of Internal Medicine, Pitié-Salpêtrière Hospital, Paris, France.

N Martin-Duverneuil (N)

APHP, Department of Neuroradiology, Pitié-Salpêtrière Hospital, Paris, France.

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Classifications MeSH