家族性遗传性淋巴水肿又称 Nonne-Milroy-Meige 综合征或先天性阿拉伯象皮肿,临床少见,现将我们见到的母女二例报告如下:病历摘要例1 女,52岁。17岁时发现右足逐渐肿大,无发热及其他不适。次年春季,双足踝部红肿、疼痛,压之较硬,压痛(+),活动受限,乏力、纳差,恶心、呕吐,体温达40.0℃。住某医院,诊断“双下肢急性淋巴管炎”,经消炎治疗,热退,但足踝部肿胀不见消退。此后,双下肢肿大范围逐渐上升,平 Familial hereditary lymphedema, also known as Nonne-Milroy-Meige syndrome or congenital Arab elephantiasis, clinical rare, we will now see two cases of mother and daughter are as follows: Case Summary 1 female, 52 years old. 17-year-old found that right foot gradually enlarged, no fever and other discomfort. The next spring, both feet ankle swelling, pain, hard pressure, tenderness (+), limited mobility, fatigue, anorexia, nausea, vomiting, body temperature reached 40.0 ℃. Live in a hospital, the diagnosis of “double lower extremity acute lymphangitis,” anti-inflammatory treatment, heat back, but the foot ankle swelling disappear. Since then, double lower extremity swelling range gradually increased, flat