Kutanes Rosai-Dorfman-Syndrom
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  • 作者:Dr. S. Vandersee (1)
    H.-J. R?wert-Huber (1)
    S. W?hner (2)
    C. Loddenkemper (3)
    M. Beyer (1)
    D. Humme (1)
  • 关键词:Methotrexat ; Nicht ; Langerhans ; Zell ; Histiozytose ; Seltene Erkrankung ; Triamcinolon ; Histiozyten ; Methotrexate ; Non ; Langerhans cell histiocytoses ; Rare condition ; Triamcinolone ; Histiocytes
  • 刊名:Der Hautarzt
  • 出版年:2014
  • 出版时间:August 2014
  • 年:2014
  • 卷:65
  • 期:8
  • 页码:725-727
  • 全文大小:1,900 KB
  • 参考文献:1. Rosai J, Dorfman RF (1969) Sinus histiocytosis with massive lymphadenopathy. A newly recognized benign clinicopathological entity. Arch Pathol 87:63-0
    2. Thawerani H, Sanchez RL, Rosai J, Dorfman RF (1978) The cutaneous manifestations of sinus histiocytosis with massive lymphadenopathy. Arch Dermatol 114:191-97 CrossRef
    3. Newman B, Hu W, Nigro K, Gilliam AC (2007) Aggressive histiocytic disorders that can involve the skin. J Am Acad Dermatol 56:302-16 CrossRef
    4. Landim FM, Rios Hde O, Costa CO et al (2009) Cutaneous Rosai-Dorfman disease. An Bras Dermatol 84:275-78 CrossRef
    5. Wang KH, Chen WY, Liu HN et al (2006) Cutaneous Rosai-Dorfman disease: clinicopathological profiles, spectrum and evolution of 21 lesions in six patients. Br J Dermatol 154:277-86 CrossRef
    6. Salva KA, Stenstrom M, Breadon JY et al (2014) Possible association of cutaneous rosai-dorfman disease and chronic crohn disease: a case series report. JAMA Dermatol 150:177-81 CrossRef
    7. Frater JL, Maddox JS, Obadiah JM, Hurley MY (2006) Cutaneous Rosai-Dorfman disease: comprehensive review of cases reported in the medical literature since 1990 and presentation of an illustrative case. J Cutan Med Surg 10:281-90
    8. Xia JX, Jin XH, Mou Y et al (2013) Combined treatment for cutaneous Rosai-Dorfman disease: a report of 2 cases. Int J Clin Exp Med 6:822-27
    9. Vuong V, Moulonguet I, Cordoliani F et al (2013) Cutaneous revelation of Rosai-Dorfman disease: 7 cases. Ann Dermatol Venereol 140:83-0 CrossRef
    10. Gebhardt C, Averbeck M, Paasch U et al (2009) A case of cutaneous Rosai-Dorfman disease refractory to imatinib therapy. Arch Dermatol 145:571-74 CrossRef
    11. Horneff G, Jürgens H, Hort W et al (1996) Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease): response to methotrexate and mercaptopurine. Med Pediatr Oncol 27:187-92 CrossRef
  • 作者单位:Dr. S. Vandersee (1)
    H.-J. R?wert-Huber (1)
    S. W?hner (2)
    C. Loddenkemper (3)
    M. Beyer (1)
    D. Humme (1)

    1. Hauttumorcentrum der Charité, Klinik für Dermatologie, Venerologie und Allergologie, Charité Universit?tsmedizin Berlin, Charitéplatz 1, 10117, Berlin, Deutschland
    2. Onkologische Schwerpunktpraxis Tiergarten, Berlin, Deutschland
    3. PathoTres Gemeinschaftspraxis für Pathologie, Berlin, Deutschland
  • ISSN:1432-1173
文摘
Background Cutaneous Rosai-Dorfman disease is a rare disorder belonging to the spectrum of non-Langerhans cell histiocytoses. It is characterized by dermal and subcutaneous infiltrates of histiocytes as well as accompanying lymphocytes, plasma cells and granulocytes. Because it is so rare, standard therapies have not been established. Case report A 27-year-old man showed an excellent response to intralesional corticosteroids after unsuccessful prior treatment with methotrexate, systemic steroids and surgery as well as laser therapy.

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