Hypopigmented Mycosis Fungoides with Large Cell Transformation in a Child

被引:4
|
作者
Pradhan, Dinesh [1 ]
Jedrych, Jaroslaw J. [2 ]
Ho, Jonhan [2 ]
Akilov, Oleg E. [3 ]
机构
[1] Univ Pittsburgh, Med Ctr, Dept Pathol, Pittsburgh, PA USA
[2] Univ Pittsburgh, Dermatopathol Unit, Pittsburgh, PA USA
[3] Univ Pittsburgh, Dept Dermatol, Cutaneous Lymphoma Program, Pittsburgh, PA 15260 USA
关键词
CUTANEOUS LYMPHOMA; SERIES;
D O I
10.1111/pde.13233
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Hypopigmented mycosis fungoides (HMF) is the most common variant of mycosis fungoides (MF) in children. Large-cell transformation in HMF has never been reported. Herein we report a case of HMF in an 8-year-old boy who presented with a 6-year history of hypopigmented patches on the bilateral arms, lower back, buttocks, posterior thighs, and lower legs. Biopsy revealed an abnormal CD8(+) epidermotropic T-cell infiltrate consistent with the diagnosis of MF. The T-cell clonality study was positive. The patient was started on narrowband ultraviolet B (NBUVB) phototherapy and topical steroids. He had a 50% reduction in his patches after 10 months of treatment, after which he developed a single annular plaque on his left thigh. The biopsy specimen demonstrated large cells that were diffusely CD8(+) and CD30(-). Clobetasol propionate ointment was prescribed, which led to complete resolution of the plaque within 2 weeks. NBUVB phototherapy was continued and the patient had a complete response within the following 5 months. The case is an example of exceptionally rare large-cell transformation in pediatric MF and stresses the importance of regular follow-up of these patients.
引用
收藏
页码:E260 / E264
页数:5
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