罕见的弥漫性新生儿血管瘤病病例报告和文献综述。

IF 1.4 Q3 PEDIATRICS
Global Pediatric Health Pub Date : 2024-02-20 eCollection Date: 2024-01-01 DOI:10.1177/2333794X241227043
Fatima Zahrae El Mansoury, Zakia El Yousfi, Mohamed Ismail Halfi, Najlae Lrhorfi, Nazik Allali, Latifa Chat
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引用次数: 0

摘要

弥漫性新生儿血管瘤病(DNH)是一种不常见的疾病,其特点是同时出现多个皮肤血管瘤并累及 3 个或更多器官。如果在婴儿皮肤上发现多个血管瘤,就应怀疑是 DNH。虽然 DNH 是良性的,但它可能导致危及生命的严重并发症。诊断主要依靠临床评估,同时也非常重视影像学技术。在本病例报告中,我们介绍了一例不寻常的弥漫性婴儿血管内皮瘤儿科病例,其检查方法包括超声波和 CT 扫描。这些成像方法有助于发现肝脏、甲状腺和大脑中存在的病变,最终为诊断 DNH 发挥了关键作用。在为期 3 个月的随访中,通过皮质类固醇治疗,患者的临床和生物学状况得到了积极改善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unusual Case of Diffuse Neonatal Hemangiomatosis Case Report and Literature Review.

Diffuse neonatal hemangiomatosis (DNH) is an infrequent condition characterized by the simultaneous occurrence of multiple cutaneous hemangiomas and the involvement of 3 or more organs. DNH is suspected when multiple hemangiomas are identified on the skin of the infant. Although it is benign in nature, DNH can lead to critical and life-threatening complications. Diagnosis primarily relies on clinical evaluation with a significant emphasis on imaging techniques. In this case report, we present an unusual pediatric case of diffuse infantile hemangioendothelioma, for which the investigative approach included ultrasound and CT scans. These imaging methods were instrumental in revealing the presence of lesions in the liver, thyroid, and brain, ultimately playing a pivotal role in making the diagnosis of DNH. A positive clinical and biological improvement was observed with corticosteroid treatment during a 3-month follow-up.

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来源期刊
Global Pediatric Health
Global Pediatric Health Nursing-Pediatrics
CiteScore
2.20
自引率
0.00%
发文量
105
审稿时长
12 weeks
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