Primary cutaneous CD4+ small/medium T-cell lymphoproliferative disorder in children: A case report and review of the literature

被引:4
|
作者
Plumptre, Isabella R. [1 ]
Said, Jordan T. [2 ,3 ]
Sheu Song, Johanna [2 ]
Corey, Kristen [3 ,4 ]
LeBoeuf, Nicole R. [3 ,4 ,5 ]
机构
[1] Imperial Coll Healthcare NHS Trust, London, England
[2] Brigham & Womens Hosp, Dept Dermatol, 75 Francis St, Boston, MA 02115 USA
[3] Harvard Med Sch, Boston, MA 02115 USA
[4] Boston Childrens Hosp, Dept Dermatol, Boston, MA USA
[5] Dana Farber Canc Inst, Ctr Cutaneous Oncol, 375 Longwood Ave, Boston, MA 02115 USA
关键词
lymphoproliferative disorder; PCSM-TCLPD; pediatric cutaneous oncology; pediatric oncology; peripheral T-cell lymphoproliferative disorder; primary cutaneous CD4(+) small; medium T-cell lymphoproliferative disorder; LYMPHOMA; MULTICENTER; CD4+SMALL; PATIENT; SERIES;
D O I
10.1002/pbc.29862
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Primary cutaneous CD4(+) small/medium T-cell lymphoproliferative disorder (PCSM-TCLPD) is a rare benign lymphoproliferative disorder, recently redefined by the 2016 World Health Organization classification of lymphoid neoplasms. In adults, PCSM-TCLPD responds well to monotherapy with surgical excision or local radiation, with or without topical/injected corticosteroids; in contrast, PCSM-TCLPD has only rarely been reported in children, in whom treatments favored in adults may be non-optimal. We present a 14-year-old male with PCSM-TCLPD on the forehead, who achieved complete remission following biopsy, topical corticosteroids, and surgical excision. We also review all literature-reported cases of pediatric PCSM-TCLPD, emphasizing the disorder's benign nature and treatment responsiveness in children.
引用
收藏
页数:4
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