Co-existent primary cutaneous anaplastic large cell lymphoma and lymphomatoid papulosis

被引:5
作者
Dawn, G [1 ]
Morrison, A
Morton, R
Bilsland, D
Jackson, R
机构
[1] So Gen Hosp, Dept Dermatol, Glasgow G51 4TF, Lanark, Scotland
[2] So Gen Hosp, Dept Haematol, Glasgow G51 4TF, Lanark, Scotland
[3] So Gen Hosp, Dept Pathol, Glasgow G51 4TF, Lanark, Scotland
[4] Royal Infirm, Dept Pathol, Glasgow G31 2ER, Lanark, Scotland
关键词
D O I
10.1046/j.1365-2230.2003.01406.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
We describe the case of a 37-year-old female with a history of psoriasiform dermatitis who presented with multicentric primary cutaneous CD30-positive anaplastic large T cell lymphoma (ALCL). Despite aggressive systemic therapy, the patient suffered multiple relapses and the lymphoma spread to cervical and inguinal lymph nodes. Later in her clinical course it was appreciated that she was also suffering from lymphomatoid papulosis (LyP). The case illustrates the overlapping clinical, histological and immunophenotypic features of ALCL and LyP, conditions which represent a spectrum of CD30-positive lymphoproliferative disease. A multidisciplinary approach between dermatologist, oncologist and pathologist is essential for the optimal management of these complex conditions.
引用
收藏
页码:620 / 624
页数:5
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