Multifocal congenital pyogenic granuloma successfully treated with oral propranolol

被引：7

作者：

Alharbi, Mana ^{[1
]}

Eber, Ariel E. ^{[2
]}

Perper, Marina ^{[2
]}

ALFalah, Maisa ^{[3
]}

Al-Khenaizan, Sultan ^{[3
]}

Alomair, Ibrahim A. ^{[1
]}

Alfuraih, Abdulkareem ^{[4
]}

Nouri, Keyvan ^{[2
]}

Cho-Vega, Jeong Hee ^{[5
,6
]}

机构：

[1] Imam Muhammad ibn Saud I Univ IMSIU, Dermatol Dept, Riyadh, Saudi Arabia

[2] Univ Miami, Miller Sch Med, Dept Dermatol & Cutaneous Surg, Miami, FL 33136 USA

[3] King Abdul Aziz Med City, Dermatol Dept, Riyadh, Saudi Arabia

[4] Secur Forces Hosp, Dermatol Dept, Riyadh, Saudi Arabia

[5] Univ Miami, Dept Pathol & Lab Med, Dermatopathol Div, Sylvester Comprehens Canc Ctr, Miami, FL 33136 USA

[6] Univ Miami, Miller Sch Med, Miami, FL 33136 USA

来源：

PEDIATRIC DERMATOLOGY | 2019年 / 36卷 / 01期

关键词：

hemangiomas/vascular tumors; therapy-systemic; HEMANGIOMA;

D O I：

10.1111/pde.13689

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

Disseminated congenital pyogenic granuloma (DCPG) is an uncommon condition. Individual lesions of DCPG share clinical and histologic similarities with infantile hemangioma (IH); endothelial glucose transporter 1 (GLUT-1), which is highly expressed in IH but generally not in pyogenic granulomas (PG), is an important diagnostic tool. Treatment for DCPG remains difficult. We describe a case of DCPG effectively treated with propranolol.

引用

页码：E41 / E43

页数：3

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