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The clinico-pathological spectrum of primary cutaneous lymphoma other than mycosis fungoides/Sezary syndrome.
Oschlies, Ilske; King, Rebecca L; Dotlic, Snjezana; Montes-Moreno, Santiago; Ponzoni, Maurilio; Traverse-Glehen, Alexandra; Calaminici, Maria; Ferry, Judith A; Ott, German; Goodlad, John R.
Afiliación
  • Oschlies I; Department of Pathology, Hematopathology Section and Lymph Node Registry, University Hospitals Schleswig-Holstein, Christian-Albrecht-University, Kiel, Germany.
  • King RL; Division of Hematopathology, Mayo Clinic, Rochester, MN, USA.
  • Dotlic S; Department of Pathology and Cytology, University Hospital Centre Zagreb, Zagreb, Croatia.
  • Montes-Moreno S; Department of Anatomic Pathology, Translational Hematopathology Lab, Hospital Universitario Marques de Valdecilla/IDIVAL, Santander, Spain.
  • Ponzoni M; Ateneo Vita-Salute San Raffaele and Unit of Lymphoid Malignancies, San Raffaele Scientific Institute, Milan, Italy.
  • Traverse-Glehen A; Department of Hematopathology, Hospices Civils de Lyon/Université Lyon 1, Lyon, France.
  • Calaminici M; Department of Cellular Pathology, SIHMDS, Barts Health NHS Trust and Centre for Haemato-Oncology, Barts Cancer Institute, London, UK.
  • Ferry JA; Department of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
  • Ott G; Department of Clinical Pathology, Robert-Bosch-Krankenhaus, Stuttgart, Germany.
  • Goodlad JR; Department of Pathology, Queen Elizabeth University Hospital, Level 3, Laboratory Medicine Building, 1345 Govan Rd, Glasgow, G51 4TF, Scotland. john.goodlad@nhs.net.
Virchows Arch ; 476(5): 683-699, 2020 May.
Article en En | MEDLINE | ID: mdl-31781845
The major aim of Session 1 of the 2018 European Association of Hematopathology/Society for Hematopathology Workshop was to collect examples of cutaneous lymphomas, excluding mycosis fungoides/Sezary syndrome, as defined in the current WHO classification of tumours of the haemetopoietic and lymphoid tissues. Overall 42 cases were submitted. These were considered in four main categories: primary cutaneous B cell lymphomas (12 cases), primary cutaneous T cell lymphomas/lymphoproliferations with CD8+/cytotoxic phenotype (12 cases), primary cutaneous CD30-positive lymphoproliferative disorders (15 cases) and primary cutaneous T cell lymphomas/leukaemias with CD4+ phenotype (4 cases). Using these cases as examples, we were able to present the full spectrum of cutaneous lymphoproliferations (excluding mycosis fungoides/Sezary syndrome), including examples of rare, provisional and new entities as listed in the 2017 update of the WHO classification. The findings are summarized in this report with emphasis on differential diagnostic considerations and the importance of clinico-pathological correlation for final subtyping. In presenting these findings we hope to raise awareness of this enigmatic group of neoplasms and to further our understanding of these rare disease entities.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Cutáneas / Leucemia / Linfoma de Células B / Linfoma Cutáneo de Células T / Trastornos Linfoproliferativos Límite: Humans Idioma: En Revista: Virchows Arch Asunto de la revista: BIOLOGIA MOLECULAR / PATOLOGIA Año: 2020 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Cutáneas / Leucemia / Linfoma de Células B / Linfoma Cutáneo de Células T / Trastornos Linfoproliferativos Límite: Humans Idioma: En Revista: Virchows Arch Asunto de la revista: BIOLOGIA MOLECULAR / PATOLOGIA Año: 2020 Tipo del documento: Article País de afiliación: Alemania
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