Center for Lymphatic and Venous Disorders, Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, California 94305, USA.
Ann N Y Acad Sci. 2010 Oct;1207 Suppl 1:E2-6. doi: 10.1111/j.1749-6632.2010.05804.x.
The visceral manifestations of lymphatic disorders (lymphangiomatosis and lymphangiectasia) are particularly severe. Any pathology of the lymphatic vasculature, whether superficial or internal, regional, or systemic, is predominated by the appearance of lymphedema, the characteristic form of tissue edema that occurs when lymphatic dysfunction supervenes. Disease manifestations may include dysregulation of body fluid homeostasis, immune traffic impairment, and disturbances of lipid and protein reabsorption from the gut lumen. The appearance of lymphatic edema invokes complex biological alterations. Many of these changes seem to relate uniquely to chronic lymphatic edema, including a profound stimulus to collagen and adipose deposition. Despite the recent advances in our understanding of these disorders, substantial knowledge gaps remain; these gaps inhibit our ability to accurately identify, categorize, treat, and prevent these diseases. Future diagnostic, therapeutic, and reproductive decisions for affected individuals require an accurate knowledge of the clinical and laboratory presentation, mode of inheritance, treatment response, outcomes, and prognosis.
淋巴系统疾病(淋巴管瘤病和淋巴管扩张症)的内脏表现尤其严重。无论浅在或内在、区域性或系统性,任何淋巴血管病理学均以淋巴水肿为主要表现,这是当淋巴功能障碍出现时发生的特征性组织水肿形式。疾病表现可能包括体液内稳态失调、免疫交通受损以及从肠道腔吸收脂质和蛋白质的紊乱。淋巴水肿的出现引发了复杂的生物学改变。其中许多变化似乎与慢性淋巴水肿有关,包括对胶原和脂肪沉积的深刻刺激。尽管我们对这些疾病的理解最近有所进展,但仍存在大量知识空白;这些空白阻碍了我们准确识别、分类、治疗和预防这些疾病的能力。受影响个体的未来诊断、治疗和生殖决策需要准确了解临床和实验室表现、遗传模式、治疗反应、结果和预后。