KI-1-POSITIVE LARGE-CELL CUTANEOUS LYMPHOMA MIMICKING A STEWART-TREVES ANGIOSARCOMA

被引：14

作者：

BEYLOTBARRY, M ^{[1
]}

VERGIER, B ^{[1
]}

BEYLOT, C ^{[1
]}

DEMASCAREL, A ^{[1
]}

DOUTRE, MS ^{[1
]}

机构：

[1] CHU BORDEAUX,HOP HAUT LEVEQUE,ANATOMOPATHOL LAB,F-33604 PESSAC,FRANCE

来源：

DERMATOLOGY | 1995年 / 190卷 / 01期

关键词：

ANAPLASTIC LARGE-CELL LYMPHOMA; STEWART-TREVES SYNDROME; IMMUNOHISTOCHEMISTRY; CHRONIC LYMPHEDEMA;

D O I：

10.1159/000246641

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

Anaplastic large-cell cutaneous lymphomas (ALCL) represent a heterogeneous group. Primitive cutaneous lymphomas are exceptional, sometimes with a deceptive clinical aspect, but must be considered as a distinct clinicopathologic entity, We report a case of a cutaneous ALCL, appearing 7 years after a homolateral Hodgkin ganglionic lymphoma and occurring on a chronic lymphoedema of the arm. A Stewart-Treves angiosarcoma was suggested owing to its location, vascular aspect and low histologic differentiation. Immunohistochemistry was helpful in making the diagnosis of ALCL. Southern blotting analysis revealed a rearrangement of the beta-chain of the T-receptor gene, thus suggesting the T-cell origin of this lymphoma.

引用

页码：77 / 82

页数：6

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