间变性淋巴瘤激酶
间变性大细胞淋巴瘤
CD30
淋巴瘤
大细胞
医学
病理
大细胞淋巴瘤
淋巴增殖性病變
免疫组织化学
癌症研究
癌症
内科学
腺癌
恶性胸腔积液
肺癌
作者
Ilske Oschlies,Jasmin Lisfeld,Laurence Lamant,Atsuko Nakazawa,Emanuele S G d'Amore,Ulrika Hansson,Konnie M. Hebeda,Ingrid Simonitsch‐Klupp,Jadwiga Małdyk,Leonhard Müllauer,Marianne Tinguely,Markus Stücker,Marie-cecile Ledeley,Reiner Siebert,Alfred Reiter,Laurence Brugières,Wolfram Klapper,Wilhelm Woessmann
出处
期刊:Haematologica
[Ferrata Storti Foundation]
日期:2012-07-06
卷期号:98 (1): 50-56
被引量:107
标识
DOI:10.3324/haematol.2012.065664
摘要
Anaplastic large cell lymphomas are peripheral T-cell lymphomas that are characterized by a proliferation of large anaplastic blasts expressing CD30. In children, systemic anaplastic large cell lymphomas often present at advanced clinical stage and harbor translocations involving the anaplastic lymphoma kinase (ALK) gene leading to the expression of chimeric anaplastic lymphoma kinase (ALK)-fusion proteins. Primary cutaneous anaplastic large cell lymphoma is regarded as an ALK-negative variant confined to the skin and is part of the spectrum of primary cutaneous CD30-positive T-cell lymphoproliferative disorders. Thirty-three of 487 pediatric patients registered within the Anaplastic Large Cell Lymphoma-99 trial (1999 to 2006) presented with a skin limited CD30-positive lympho-proliferative disorder. In 23 of the 33 patients, material for international histopathological review was available, and the cases were studied for histopathological, immunophenotypical and clinical features as well as for breaks within the ALK gene. Five of 23 cases and one additional case (identified after closure of the trial) expressed ALK-protein. Complete staging excluded any other organ involvement in all children. Expression of ALK proteins was demonstrated by immunohistochemistry in all cases and the presence of breaks of the ALK gene was genetically confirmed in 5 evaluable cases. The histopathological and clinical picture of these skin-restricted ALK-positive lymphomas was indistinguishable from that of cutaneous anaplastic large cell lymphoma. Five children presented with a single skin lesion that was completely resected in 4 and incompletely resected in one. Three of these patients received no further therapy, 2 additional local radiotherapy, and one chemotherapy. All children remain in complete remission with a median follow up of seven years (range 1-8 years). We present 6 pediatric cases of ALK-positive primary cutaneous anaplastic large cell lymphomas. After thorough exclusion of systemic involvement, therapy confined to local measures seems to be sufficient to induce cure.
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