A case of anaplastic lymphoma kinase-positive anaplastic large cell lymphoma presenting with spontaneous splenic rupture: an extremely unusual presentation

被引:0
作者
K. M. Hebeda
M. A. MacKenzie
J.H.J.M. van Krieken
机构
[1] Department of Pathology,
[2] UMC St. Radboud,undefined
[3] PO Box 9101,undefined
[4] 6500 HB Nijmegen,undefined
[5] The Netherlands Tel.: +31-24-3614314 Fax: +31-24-3540520,undefined
[6] Department of Hematology,undefined
[7] UMC St. Radboud,undefined
[8] PO Box 9101,undefined
[9] 6500 HB Nijmegen,undefined
[10] The Netherlands,undefined
来源
Virchows Archiv | 2000年 / 437卷
关键词
Keywords Non-Hodgkin’s lymphoma; Immunohistochemistry; ALK1; T-cell lymphoma; Splenic rupture;
D O I
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学科分类号
摘要
In a 22-year-old male with a 10-day history of fever, painful swelling in the left groin, and abdominal complaints, emergency surgery was performed because of spontaneous splenic rupture. At histology, a cellular infiltrate of intermediate-sized atypical lymphocytes was seen in the splenic white pulp, staining for T-cell markers. In addition, CD30 and anaplastic lymphoma kinase 1 (ALK) were diffusely positive, thus, representing a case of anaplastic large cell lymphoma (ALCL), T-cell, ALK-positive, small cell monomorphic variant. ALK-positive ALCL patients generally bear a much better prognosis than patients with T-cell lymphomas, unspecified, or ALK-negative ALCL. Therefore, besides the very unusual clinical presentation, this case highlights the importance of immunostaining for CD30 and ALK in all T-cell lymphomas. This report is the first extensive description of ALK-positive ALCL involvement of the spleen.
引用
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页码:459 / 464
页数:5
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