Kerhoas Nicolas C K, Le Bidaut M, Dosquet C, Enjolras O, Stalder J F
Clinique Dermatologique, CHU Hôtel-Dieu, Nantes.
Ann Dermatol Venereol. 1997;124(12):852-4.
Kasabach-Merritt syndrome and Gorham's sign are two uncommon and severe, sometimes life-threatening, complications in infants with vascular lesions. Their association has been described in rare cases.
An infant with a vast congenital angiomatous lesion including an extensive lymphatic component, developed active regional osteolysis then suddenly suffered disseminated intravascular coagulation of the leg. Medical treatment was unsatisfactory. After unsuccessful use of low molecular weight heparin, pentoxifyllin and alpha interferon, amputation of the leg was required to avoid a fatal outcome.
Kasabach-Merritt syndrome does not develop on classic immature hemangiomas, despite some contradictory statements in the literature. In our case, a complex tumor developed in association with a lymphatic malformation. The association of Kasabach-Merritt syndrome with osteolysis (Gorham's sign) does not appear to be fortuitous. Therapeutic management of these severe complications is difficult and requires case by case analysis.
卡萨巴赫 - 梅里特综合征和戈勒姆征是血管病变婴儿中两种罕见且严重、有时危及生命的并发症。它们的关联在罕见病例中有所描述。
一名患有巨大先天性血管瘤病变(包括广泛淋巴成分)的婴儿,出现了活动性局部骨质溶解,随后突然发生腿部弥散性血管内凝血。药物治疗效果不佳。在低分子量肝素、己酮可可碱和α干扰素使用失败后,为避免致命后果,需要截肢。
尽管文献中有一些矛盾的说法,但卡萨巴赫 - 梅里特综合征不会在典型的未成熟血管瘤上发生。在我们的病例中,一种复杂的肿瘤与淋巴管畸形相关联。卡萨巴赫 - 梅里特综合征与骨质溶解(戈勒姆征)的关联似乎并非偶然。这些严重并发症的治疗管理困难,需要逐案分析。