Solitary intracerebral langerhans cell histiocytosis: report of one case and literature review

被引:2
作者
Mathis, S.
Levillain, P.
Vandermarcq, P.
Gil, R.
Auche, V.
Ciron, J.
Neau, J.-P.
机构
[1] Univ Poitiers, CHU Poitiers, Neurol Clin, F-86021 Poitiers, France
[2] Univ Poitiers, CHU Poitiers, Serv Anat & Cytol Pathol, F-86021 Poitiers, France
[3] Univ Poitiers, CHU Poitiers, Serv Radiol, F-86021 Poitiers, France
来源
REVUE DE MEDECINE INTERNE | 2007年 / 28卷 / 09期
关键词
langerhans cell histiocytosis; histiocytosis X; neurological manifestations; focal intracerebral lesion;
D O I
10.1016/j.revmed.2007.04.018
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction. - Langerhans cell histiocytosis is a multivisceral pathology. Neurological manifestations are rare. Exegesis. - We report the case of a 31 year old man hospitalized for left partial motor seizure revealing a right frontal tumor with criteria for histiocytosis X. The histological and biological examination found criteria for Langerhans cell histiocytosis (CDIa and S100 reactivity). The check-up for extracerebral localisations of the disease was negative. The outcome was favourable after a total surgical resection. The review of the literature and a discussion on neurological manifestations of this disease were carried out. Conclusion. - A neurological manifestation can be the first and only symptom of a Langerhans cell histiocytosis. (c) 2007 Elsevier Masson SAS. Tous droits reserves.
引用
收藏
页码:645 / 650
页数:6
相关论文
共 45 条
[1]   Langerhans cell histiocytosis in adults report from the International Registry of the Histiocyte Society [J].
Aricò, M ;
Girschikofsky, M ;
Généreau, T ;
Klersy, C ;
McClain, K ;
Grois, N ;
Emile, JF ;
Lukina, E ;
De Juli, E ;
Danesino, C .
EUROPEAN JOURNAL OF CANCER, 2003, 39 (16) :2341-2348
[2]   Solitary Langerhans cell histiocytosis lesion of the parieto-occipital lobe: A case report and review of the literature [J].
Bergmann, M ;
Yuan, Y ;
Bruck, W ;
Palm, KV ;
Rohkamm, R .
CLINICAL NEUROLOGY AND NEUROSURGERY, 1997, 99 (01) :50-55
[3]   DIAGNOSIS OF ATYPICAL INTRACEREBRAL LANGERHANS CELL HISTIOCYTOSIS SUGGESTED BY CONCOMITANT LUNG ABNORMALITIES [J].
BOGAERT, J ;
VERSCHAKELEN, JA ;
DHAEN, B ;
DOM, R ;
WILMS, G .
FORTSCHRITTE AUF DEM GEBIETE DER RONTGENSTRAHLEN UND DER NEUEN BILDGEBENDEN VERFAHREN, 1994, 161 (04) :369-371
[4]  
Boralevi F, 1998, ANN DERMATOL VENER, V125, P335
[5]   CEREBRAL AND BRAIN-STEM LANGERHANS CELL HISTIOCYTOSIS [J].
BREIDAHL, WH ;
IVES, FJ ;
KHANGURE, MS .
NEURORADIOLOGY, 1993, 35 (05) :349-351
[6]   Langerhans cell histiocytosis with central nervous system involvement:: Follow-up by FDG-PET during treatment with cladribine [J].
Büchler, T ;
Cervinek, L ;
Belohlavek, O ;
Kantorova, I ;
Mechl, M ;
Nebesky, T ;
Vorlicek, J ;
Adam, Z .
PEDIATRIC BLOOD & CANCER, 2005, 44 (03) :286-288
[7]   Brain 18-FDG PET scan in central nervous system Langerhans cell histiocytosis [J].
Calming, U ;
Bemstrand, C ;
Mosskin, M ;
Elander, SS ;
Ingvar, M ;
Henter, JI .
JOURNAL OF PEDIATRICS, 2002, 141 (03) :435-440
[8]  
CARESIO JF, 1991, AM J NEURORADIOL, V12, P82
[9]   PRIMARY EOSINOPHILIC GRANULOMA OF THE FRONTAL-LOBE [J].
CERDANICOLAS, M ;
BROSETA, J ;
PEYDROOLAYA, A ;
BARBERA, J ;
BARCIASALORIO, JL ;
LLOMBARTBOSCH, A .
VIRCHOWS ARCHIV A-PATHOLOGICAL ANATOMY AND HISTOPATHOLOGY, 1980, 388 (02) :221-228
[10]  
Donadieu J, 1996, ARCH DIS CHILD, V75, P17