Oktay Burcu Kılınç, Kaçar Ayşe Gonca, Özel Simge Çınar, Ocak Süheyla, Celkan Tiraje
Division of Pediatric Hematology-Oncology, Department of Pediatrics, Istanbul University-Cerrahpaşa, Cerrahpaşa School of Medicine, Istanbul, Turkey.
Turk Arch Pediatr. 2021 May 1;56(3):213-218. doi: 10.5152/TurkArchPediatr.2021.20089. eCollection 2021.
Difficulties encountered in the diagnosis and treatment of vascular anomalies located in the extremities of the children. The most common vascular lesions are hemangiomas and venous malformations. The complex malformations, such as, Klippel-Trenaunay Syndrome are much less commonly encountered lesions. Treatment of vascular malformations are variable based on the etiology of the lesion and clinical presentation. In this study, we aimed to share our experience on the clinical features of vascular lesions in the extremities of the children.
The demographic, clinical and prognostic features of 330 children with vascular anomalies followed at IUC, Cerrahpasa Medical Faculty, Department of Pediatric Hematology and Oncology were retrospectively reviewed. Fifty-one patients with lesions >5 cm in diameter were included into the study. The diagnosis, age, sex, history of prematurity, lesion type and location, imaging and biopsy findings, complications, details of treatment, and follow-up were evaluated.
Twenty-nine (57%) of patients were female and 22 (43%) were male. The female to male ratio was 1.3:1. The median age at admission was 15 months (10 days-180 months). Eight patients (16%) had a history of premature birth. Thirty-one patients (61%) had lesions since birth, eight lesions (8%) appeared in the first month of life and 6 (12%) occurred after 1 year of age. Sixteen of the patients (31%) had hemangioma, 11 (22%) had lymphangioma, 19 (37%) had venous malformation and 5 (10%) were diagnosed as Klippel Trenaunay Syndrome. The lesions were in the upper extremity in 21 patients (41%), in the lower extremity in 27 patients (53%), and both lower and upper extremities were affected in 3 patients (6%). Of all patients, six had intramuscular and two had intraarticular lesions. The diagnosis was made on clinical grounds in most of the cases. In 22 children Magnetic Resonance Imaging was performed for differential diagnosis and to demonstrate the infrastructure of the lesion and the extent of local infiltration. Histopathologic examination by biopsy was done in four patients. Complications developed in 19 patients as follows: Disseminated intravascular coagulation in 6, bleeding in 4, thrombosis in 3, and soft tissue infection in 6. Twenty-one patients were not given any treatment. Medical treatments were propranolol in 14 patients, sirolimus in 4 patients, propranolol and sirolimus in 5 patients. Intralesional bleomycin injection was performed in 3 children.
The diagnosis, classification and treatment of extremity located vascular malformations in children are complex. Treatment strategy should be defined as in accordance with a combination of the type of the vascular malformation, the age of the patient and the clinical picture.
探讨儿童四肢血管异常在诊断和治疗中遇到的困难。最常见的血管病变是血管瘤和静脉畸形。像克-特综合征这样的复杂畸形则是较少见的病变。血管畸形的治疗因病变的病因和临床表现而异。在本研究中,我们旨在分享我们关于儿童四肢血管病变临床特征的经验。
回顾性分析了在伊斯坦布尔大学塞拉哈帕夏医学院儿科血液学和肿瘤学系随访的330例血管异常患儿的人口统计学、临床和预后特征。将51例直径>5 cm的病变患儿纳入研究。评估了诊断、年龄、性别、早产史、病变类型和部位、影像学和活检结果、并发症、治疗细节及随访情况。
29例(57%)为女性,22例(43%)为男性。男女比例为1.3:1。入院时的中位年龄为15个月(10天至180个月)。8例(16%)有早产史。31例(61%)自出生即有病变,8例(8%)在出生后第一个月出现病变,6例(12%)在1岁后出现病变。16例(31%)为血管瘤,11例(22%)为淋巴管瘤,19例(37%)为静脉畸形,5例(10%)诊断为克-特综合征。21例(41%)病变位于上肢,27例(53%)位于下肢,3例(6%)上下肢均受累。所有患者中,6例有肌肉内病变,2例有关节内病变。大多数病例根据临床表现做出诊断。22例患儿进行了磁共振成像以进行鉴别诊断并显示病变的结构和局部浸润范围。4例患者进行了活检组织病理学检查。19例患者出现并发症,如下:6例发生弥散性血管内凝血,4例出血,3例血栓形成,6例软组织感染。21例患者未接受任何治疗。14例患者接受普萘洛尔治疗,4例接受西罗莫司治疗,5例接受普萘洛尔和西罗莫司治疗。3例患儿进行了瘤内博来霉素注射。
儿童四肢血管畸形的诊断、分类和治疗较为复杂。治疗策略应根据血管畸形的类型、患者年龄和临床表现综合确定。