Search our Database of Scientific Publications and Authors

I’m looking for a

    Details and Download Full Text PDF:
    A Case of Primary Cutaneous Aggressive Epidermotropic CD8+ Cytotoxic T-cell Lymphoma Misdiagnosed as Febrile Ulceronecrotic Mucha-Habermann Disease.

    • Authors:
    • Nan Sheng
      University of Pittsburgh
      United States
      ZhiLiang Li
      Chongqing University
      China
      Wei Su
      Guangxi Teachers Education University
      China
      Weijun Liu
      University of Pittsburgh School of Medicine and University of Pittsburgh Cancer Institute
      United States
      Wenkai Zong
      Institute of Dermatology
      Wuhan Shi | China
      Baoxi Wang
      Peking Union Medical College Hospital
      China
      Suying Feng
      Institute of Dermatology
      China
    Acta Derm Venereol 2016 Jan;96(1):136-7
    Jiangsu Key Laboratory of Molecular Biology for Skin Diseases and STIs,Institute of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College, Jiangwangmiao Street 12, Nanjing, Institute of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College, Jiangwangmiao Street 12, Nanjing, Jiangsu 210042, China.
    PDF Download - Full Text Link
    ( Please be advised that this article is hosted on an external website not affiliated with PubFacts.com)
    Source Status
    http://dx.doi.org/10.2340/00015555-2155DOI ListingPossible

    Similar Publications

    A variant of lymphomatoid papulosis simulating primary cutaneous aggressive epidermotropic CD8+ cytotoxic T-cell lymphoma. Description of 9 cases.
    Am J Surg Pathol 2010 Aug;34(8):1168-75
    Research Unit Dermatopathology, Department of Dermatology, Medical University of Graz, Graz, Austria.
    Lymphomatoid papulosis (LyP) is a recurrent, self-healing eruption belonging to the spectrum of cutaneous CD30+lymphoproliferative disorders. Three main histologic subtypes of LyP are recognized: type A (histiocytic), type B (mycosis fungoides-(MF)-like), and type C (anaplastic large cell lymphoma-like). We reviewed 26 biopsies from 9 patients (M:F=6:3, median age: 29; mean age 27,2; age range 10 to 38) who presented with clinical features typical of LyP but with histopathologic aspects that resembled primary cutaneous aggressive epidermotropic CD8+cytotoxic T-cell lymphoma. Read More