Oral sirolimus for the treatment of juvenile xanthogranuloma: Report of two pediatric cases

被引:1
|
作者
Toker, Michelle [1 ,7 ]
Hassonjee, Fatema Esaa [2 ,3 ]
Amodio, John [3 ,4 ]
Edelman, Morris C. [5 ,6 ]
Emeghebo, Kristina I. [6 ]
Levy, Carolyn Fein [3 ,6 ]
Shaigany, Sheila [2 ,3 ]
机构
[1] Albert Einstein Coll Med, Bronx, NY 10461 USA
[2] Long Isl Jewish Med Ctr, Dept Dermatol, New Hyde Pk, NY USA
[3] Donald & Barbara Zucker Sch Med Hofstra Northwell, Hempstead, NY USA
[4] Long Isl Jewish Med Ctr, Dept Radiol, New Hyde Pk, NY 11042 USA
[5] Long Isl Jewish Med Ctr, Dept Pathol, New Hyde Pk, NY USA
[6] Cohen Childrens Med Ctr, Dept Pediat, Div Hematol Oncol & Cellular Therapy, New Hyde Pk, NY USA
[7] Albert Einstein Coll Med, Montefiore Med Ctr, 1300 Morris Pk Ave, Bronx, NY 10461 USA
关键词
histiocytic disorders; juvenile xanthogranuloma (JXG); mammalian target of rapamycin (mTOR); pediatric dermatology; sirolimus; HISTIOCYTOSIS; RAPAMYCIN;
D O I
10.1111/pde.15579
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Juvenile xanthogranuloma (JXG) with extensive cutaneous or visceral organ involvement is often associated with high morbidity and treatment commonly involves surgical excision, radiotherapy, systemic steroids, or chemotherapy. Sirolimus, a mammalian target of rapamycin (mTOR) inhibitor, is an oral antitumor and immunosuppressive therapy used to treat various neoplastic disorders, including histiocytic disorders. We report two pediatric cases of JXG successfully treated with oral sirolimus monotherapy, and postulate that sirolimus may induce rapid disease resolution and long-term remission for patients with both skin-limited and multisystemic JXG. Our findings warrant further investigation of the relationship between the mTOR pathway and JXG.
引用
收藏
页码:849 / 852
页数:4
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