婴儿血管瘤的罕见并发症:卡萨巴赫-梅里特现象。

IF 0.4 Q4 SURGERY Journal of Surgical Case Reports Pub Date : 2024-11-25 eCollection Date: 2024-11-01 DOI:10.1093/jscr/rjae721
Ricardo A Caravantes, José Manuel Toralla, Daniela Saenz
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引用次数: 0

摘要

婴儿血管瘤是最常见的血管肿瘤类型,约有 5% 的婴儿在出生后几周内会患上这种肿瘤。在极少数情况下,这些肿瘤会导致卡萨巴赫-梅里特现象(Kasabach-Merritt phenomenon,KMP),这是一种危及生命的消耗性凝血病,其特点是血小板减少、微血管病性溶血性贫血和低纤维蛋白原血症。在本病例中,一名 20 个月大的患者被诊断为 KMP。本病例报告强调了诊断和管理方面的挑战,并强调了多学科方法的重要性。
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A rare complication of infantile hemangioma: Kasabach-Merritt phenomenon.

Infantile hemangiomas are the most common type of vascular tumors, affecting ~5% of infants within the first weeks of life. In rare instances, these tumors can lead to Kasabach-Merritt phenomenon (KMP), a life-threatening consumptive coagulopathy characterized by thrombocytopenia, microangiopathic hemolytic anemia, and hypofibrinogenemia. In the present case, a 20-month-old patient is diagnosed with KMP. This case report highlights the challenges in diagnosis and management, reinforcing the importance of multidisciplinary approach.

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来源期刊
CiteScore
0.70
自引率
0.00%
发文量
559
审稿时长
11 weeks
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