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先天性淋巴性水肿又称Milroy氏征,为一罕见病。本文就其临床与磁共振成像表现1例报告如下。 女,6 5/12岁,湖北省仙桃市人。出生后1个月发现颜面有水肿,7个月时双上肢相继出现水肿,水肿长期存在且逐年加重至入院。起病前后无发热、尿少,无手术及放疗史。否认有结核、风湿病和当地有丝虫病流行史,家系中无类似病史,出生后发育正常。体检:血压12/8.5kPa,智力可,呼吸平,颜面及双上肢有凹陷性无痛性弥漫性水肿,皮肤有增厚韧
Congenital lymphedema, also known as Milroy’s sign, is a rare condition. This article on its clinical and magnetic resonance imaging showed a case report below. Female, 6 5/12 years old, Xiantao City, Hubei Province. 1 month after birth, there was edema on the face. At 7 months, the upper extremities had edema one after another. Edema persisted and increased year by year. No fever before onset, less urine, no history of surgery and radiotherapy. Denied the prevalence of tuberculosis, rheumatism and endemic filariasis, no similar family history, normal development after birth. Physical examination: blood pressure 12 / 8.5kPa, intelligence can be, breathing flat, facial and upper extremity with depression painless diffuse edema, thickening of the skin tough