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皮肤和气道血管瘤中PHACE综合征的临床谱及风险

Clinical spectrum and risk of PHACE syndrome in cutaneous and airway hemangiomas.

作者信息

Haggstrom Anita N, Skillman Sarah, Garzon Maria C, Drolet Beth A, Holland Kristen, Matt Bruce, McCuaig Catherine, Metry Denise W, Morel Kimberly, Powell Julie, Frieden Ilona J

机构信息

Department of Dermatology, Indiana University, 550 N University Blvd, UH 3240, Indianapolis, IN 46202, USA.

出版信息

Arch Otolaryngol Head Neck Surg. 2011 Jul;137(7):680-7. doi: 10.1001/archoto.2011.113.

Abstract

OBJECTIVE

To describe the clinical presentation and risk of PHACE syndrome in infants with large facial hemangiomas and concomitant airway hemangiomas.

DESIGN

The study involved a case series of infants with cutaneous hemangiomas and airway hemangiomas extracted from a prospective multicenter cohort study. Data regarding clinical features, diagnosis, treatment, and clinical course were obtained from medical charts and physician intake forms. All patients were evaluated for PHACE syndrome using a standardized protocol.

SETTING

Six academic pediatric dermatology clinics.

PATIENTS

The study included 17 patients younger than 1 year who were diagnosed as having large (>22 cm(2)) facial hemangiomas and airway hemangiomas.

RESULTS

Thirteen patients (76%) had hemangiomas in the bilateral mandibular distribution. Other observed facial patterns included limited involvement of the lip and chin, unilateral reticular frontotemporal and preauricular hemangiomas, and large unilateral hemifacial hemangiomas. Fourteen patients (82%) had symptomatic airway involvement. All symptomatic patients had subglottic airway hemangiomas. The airway hemangioma was circumferential in 10 patients (58%) and more focal in distribution in 7 patients (42%). All patients were treated with oral prednisolone. Eleven patients required additional multimodal therapy. Eight patients (47%) met the criteria for PHACE syndrome.

CONCLUSIONS

Airway hemangiomas represent a potentially fatal complication of infantile hemangiomas. Our data highlight cutaneous presentations in patients with subglottic hemangiomas and large (>22 cm(2)) cutaneous hemangiomas. PHACE syndrome was detected in 8 such patients (47%) in our series.

摘要

目的

描述患有大面积面部血管瘤及伴发气道血管瘤的婴儿的PHACE综合征的临床表现及风险。

设计

本研究纳入了从一项前瞻性多中心队列研究中选取的患有皮肤血管瘤和气道血管瘤的婴儿病例系列。有关临床特征、诊断、治疗及临床病程的数据来自病历和医生接诊表格。所有患者均使用标准化方案评估是否患有PHACE综合征。

地点

六家学术性儿科皮肤科诊所。

患者

本研究纳入了17名年龄小于1岁、被诊断患有大面积(>22平方厘米)面部血管瘤和气道血管瘤的患者。

结果

13名患者(76%)的血管瘤分布于双侧下颌。其他观察到的面部表现包括唇部和下巴受累有限、单侧网状额颞部和耳前血管瘤以及大面积单侧半侧面部血管瘤。14名患者(82%)有气道受累症状。所有有症状的患者均有声门下气道血管瘤。气道血管瘤呈环状的有10名患者(58%),分布更局限的有7名患者(42%)。所有患者均接受口服泼尼松龙治疗。11名患者需要额外的多模式治疗。8名患者(47%)符合PHACE综合征标准。

结论

气道血管瘤是婴儿血管瘤的一种潜在致命并发症。我们的数据突出了声门下血管瘤和大面积(>22平方厘米)皮肤血管瘤患者的皮肤表现。在我们的系列研究中,8名此类患者(47%)检测出患有PHACE综合征。

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