eTreatment of Infantile Hemangiomas with Sirolimus in a Patient with PHACE Syndrome

被引:41
作者
Kaylani, Samer [1 ]
Theos, Amy J. [2 ]
Pressey, Joseph G. [1 ]
机构
[1] Univ Alabama Birmingham, Div Hematol Oncol, Dept Pediat, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Dept Dermatol, Birmingham, AL 35294 USA
关键词
VASCULAR ANOMALIES; STEM-CELLS; INFANCY;
D O I
10.1111/pde.12023
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Infantile hemangiomas (IHs) are common benign tumors of childhood. IHs often regress satisfactorily without intervention, but a subset of IHs may lead to functional or cosmetic morbidity necessitating therapy. PHACE syndrome is characterized by a variety of neurocutaneous and vascular anomalies that typically include segmental hemangiomas. We present an infant with PHACE syndrome and segmental IH that failed conventional first-line therapies. Treatment with sirolimus provided benefit with regression of the cutaneous IH. As an inhibitor of the mammalian target of rapamycin (mTOR) pathway, the effective use of sirolimus may shed light on the emerging role of mTOR signaling in the development and pathogenesis of IHs.
引用
收藏
页码:E194 / E197
页数:4
相关论文
共 15 条
[1]  
[Anonymous], COCHRANE DATABASE SY
[2]   Treatment of Childhood Kaposiform Hemangioendothelioma With Sirolimus [J].
Blatt, Julie ;
Stavas, Joseph ;
Moats-Staats, Billie ;
Woosley, John ;
Morrell, Dean S. .
PEDIATRIC BLOOD & CANCER, 2010, 55 (07) :1396-1398
[3]   Hemangiomas of infancy - Clinical characteristics, morphologic subtypes, and their relationship to race, ethnicity, and sex [J].
Chiller, KG ;
Passaro, D ;
Frieden, IJ .
ARCHIVES OF DERMATOLOGY, 2002, 138 (12) :1567-1576
[4]   Rapamycin causes regression of astrocytomas in tuberous sclerosis complex [J].
Franz, DN ;
Leonard, J ;
Tudor, C ;
Chuck, G ;
Care, M ;
Sethuraman, G ;
Dinopoulos, A ;
Thomas, G ;
Crone, KR .
ANNALS OF NEUROLOGY, 2006, 59 (03) :490-498
[5]   PHACE syndrome - The association of posterior fossa brain malformations, hemangiomas, arterial anomalies, coarctation of the aorta and cardiac defects, and eye abnormalities [J].
Frieden, IJ ;
Reese, V ;
Cohen, D .
ARCHIVES OF DERMATOLOGY, 1996, 132 (03) :307-311
[6]  
Frieden Ilona J, 2005, Pediatr Dermatol, V22, P383, DOI 10.1111/j.1525-1470.2005.00102.x
[7]  
Greenberger S, 2012, COLD SPRING HARB PER, V1
[8]   Rapamycin Suppresses Self-Renewal and Vasculogenic Potential of Stem Cells Isolated from Infantile Hemangioma [J].
Greenberger, Shoshana ;
Yuan, Siming ;
Walsh, Logan A. ;
Boscolo, Elisa ;
Kang, Kyu-Tae ;
Matthews, Benjamin ;
Mulliken, John B. ;
Bischoff, Joyce .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2011, 131 (12) :2467-2476
[9]   Corticosteroid Suppression of VEGF-A in Infantile Hemangioma-Derived Stem Cells. [J].
Greenberger, Shoshana ;
Boscolo, Elisa ;
Adini, Irit ;
Mulliken, John B. ;
Bischoff, Joyce .
NEW ENGLAND JOURNAL OF MEDICINE, 2010, 362 (11) :1005-1013
[10]   Sirolimus for the Treatment of Complicated Vascular Anomalies in Children [J].
Hammill, Adrienne M. ;
Wentzel, MarySue ;
Gupta, Anita ;
Nelson, Stephen ;
Lucky, Anne ;
Elluru, Ravi ;
Dasgupta, Roshni ;
Azizkhan, Richard G. ;
Adams, Denise M. .
PEDIATRIC BLOOD & CANCER, 2011, 57 (06) :1018-1024