Putra Juan, Al-Ibraheemi Alyaa
Department of Pathology, Boston Children's Hospital, and Harvard Medical School, Boston, Massachusetts, USA.
Histopathology. 2025 Jun;86(7):1032-1043. doi: 10.1111/his.15374. Epub 2024 Dec 4.
The classification and understanding of vascular anomalies have significantly evolved since the initial framework by Mulliken and Glowacki, distinguishing between vascular tumours and malformations. Recent advancements in molecular diagnostics have enhanced the accuracy of identifying and managing these complex lesions. This review provides an updated analysis of select vascular anomalies, focusing on Kaposiform hemangioendothelioma (KHE), Kaposiform lymphangiomatosis (KLA), and intramuscular fast-flow vascular anomalies. It highlights the similarities and differences between these lesions, their histopathological features, and molecular underpinnings, including key genetic mutations in the RAS/PI3K/mTOR signalling pathways. Moreover, the role of PIK3CA mutations in vascular overgrowth syndromes is explored, alongside emerging targeted therapies, such as PI3K and MEK inhibitors, that promise improved outcomes for patients with these challenging conditions. The integration of histology, molecular diagnostics, and multidisciplinary care remains critical for the accurate diagnosis and optimal treatment of vascular anomalies in the era of precision medicine.
自Mulliken和Glowacki提出最初的框架以来,血管异常的分类和理解有了显著进展,该框架区分了血管肿瘤和血管畸形。分子诊断学的最新进展提高了识别和处理这些复杂病变的准确性。本综述对选定的血管异常进行了更新分析,重点关注卡波西样血管内皮瘤(KHE)、卡波西样淋巴管瘤病(KLA)和肌肉内快速血流血管异常。它突出了这些病变之间的异同、组织病理学特征以及分子基础,包括RAS/PI3K/mTOR信号通路中的关键基因突变。此外,还探讨了PIK3CA突变在血管过度生长综合征中的作用,以及新兴的靶向治疗方法,如PI3K和MEK抑制剂,这些疗法有望改善患有这些具有挑战性疾病的患者的治疗效果。在精准医学时代,组织学、分子诊断学和多学科护理的整合对于血管异常的准确诊断和最佳治疗仍然至关重要。