Characteristic of Langerhans cell histiocytosis in oral and maxillofacial regions

被引:0
作者
Shiiba, Masashi [1 ,2 ]
Baba, Takao [2 ]
Eizuka, Keitaro [2 ]
Kasamatsu, Atsushi [2 ]
Uzawa, Katsuhiro [2 ,3 ]
Takiguchi, Yuichi [1 ]
Tanzawa, Hideki [2 ,3 ]
机构
[1] Chiba Univ, Grad Sch Med, Dept Med Oncol, Chiba, Japan
[2] Chiba Univ Hosp, Dept Dent & Oral Maxillofacial Surg, Chiba, Japan
[3] Chiba Univ, Grad Sch Med, Dept Oral Sci, Chiba, Japan
关键词
histiocyte; histiocytosis X; Langerhans cell histiocytosis (LCH); maxillofacial; oral; EOSINOPHILIC GRANULOMA; RECEPTOR; DIAGNOSIS; CHILDREN; BONE; AGE;
D O I
10.1002/osi2.1043
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Langerhans cell histiocytosis (LCH? is a rare disease caused by excessive proliferation of Langerhans cells in various regions of the body. Previous studies have reported that 10% of LCH occurs in the oral and maxillofacial regions. In the oral and maxillofacial regions, swelling and pain are the typical symptoms, and jaw fracture and tooth loss are often seen in advanced cases. In this study, we present the results of a literature review of LCH that developed in the oral and maxillofacial regions. The history, pathological conditions, diagnosis, treatment, and progress of LCH are discussed.
引用
收藏
页码:94 / 96
页数:3
相关论文
共 24 条
  • [1] [Anonymous], LANCET
  • [2] [Anonymous], 1994, INT J PEDIAT HEMATOL
  • [3] [Anonymous], WHO CLASSIFICATION T
  • [4] [Anonymous], LANGERHANS CELL HIST
  • [5] DIRECT INJECTION OF METHYLPREDNISOLONE SODIUM SUCCINATE IN THE TREATMENT OF SOLITARY EOSINOPHILIC GRANULOMA OF BONE - A REPORT OF 9 CASES
    COHEN, M
    ZORNOZA, J
    CANGIR, A
    MURRAY, JA
    WALLACE, S
    [J]. RADIOLOGY, 1980, 136 (02) : 289 - 293
  • [6] Gadner H, 2005, HISTIOCYTIC DISORDERS OF CHILDREN AND ADULTS, P229
  • [7] Management of adult patients with Langerhans cell histiocytosis: recommendations from an expert panel on behalf of Euro-Histio-Net
    Girschikofsky, Michael
    Arico, Maurizio
    Castillo, Diego
    Chu, Anthony
    Doberauer, Claus
    Fichter, Joachim
    Haroche, Julien
    Kaltsas, Gregory A.
    Makras, Polyzois
    Marzano, Angelo V.
    de Menthon, Mathilde
    Micke, Oliver
    Passoni, Emanuela
    Seegenschmiedt, Heinrich M.
    Tazi, Abdellatif
    McClain, Kenneth L.
    [J]. ORPHANET JOURNAL OF RARE DISEASES, 2013, 8
  • [8] Risk factors for diabetes insipidus in langerhans cell histiocytosis
    Grois, N
    Pötschger, U
    Prosch, H
    Minkov, M
    Arico, M
    Braier, J
    Henter, JI
    Janka-Schaub, G
    Ladisch, S
    Ritter, J
    Steiner, M
    Unger, E
    Gadner, H
    [J]. PEDIATRIC BLOOD & CANCER, 2006, 46 (02) : 228 - 233
  • [9] HISTIOCYTOSIS-X - REVIEW OF 114 CASES WITH ORAL INVOLVEMENT
    HARTMAN, KS
    [J]. ORAL SURGERY ORAL MEDICINE ORAL PATHOLOGY ORAL RADIOLOGY AND ENDODONTICS, 1980, 49 (01): : 38 - 54
  • [10] Langerhans cell histiocytosis (LCH): Guidelines for diagnosis, clinical work-up, and treatment for patients till the age of 18 years
    Haupt, Riccardo
    Minkov, Milen
    Astigarraga, Itziar
    Schaefer, Eva
    Nanduri, Vasanta
    Jubran, Rima
    Egeler, R. Maarten
    Janka, Gritta
    Micic, Dragan
    Rodriguez-Galindo, Carlos
    Van Gool, Stefaan
    Visser, Johannes
    Weitzman, Sheila
    Donadieu, Jean
    [J]. PEDIATRIC BLOOD & CANCER, 2013, 60 (02) : 175 - 184