Bektaş Hayriye, Bülbül Yılmaz, Özsu Savaş, Özlü Tevfik
Department Chest Diseases, Karadeniz Technical University Faculty of Medicine, Trabzon, Turkey.
Turk Thorac J. 2015 Jan;16(1):33-35. doi: 10.5152/ttd.2014.3988. Epub 2014 Nov 5.
Hennekam syndrome was defined as a syndrome characterized by a new autosomal recessive, severe lymphedema in legs, face and genitalia with intestinal lymphangiectasia, various face anomalies and severe mental retardation. A 21 years old male patient was examined due to bilateral pleural effusion. There were edema in both legs and eyelids, swelling in the scrotum and operation scar, broad forehead and face, depressed nasal bridge, epicanthal folds and micrognathia in the physical examination. Chylothorax was diagnosed due to level of pleural triglyceride (650 mg/dL). Lymphatic flow delayed in both lower extremities in lymphoscintigraphy. The patient was diagnosed as Hennekam syndrome due to face anomalies, lymphedema, epilepsy, chylothorax and mild mental retardation.
亨内坎综合征被定义为一种以新的常染色体隐性遗传为特征的综合征,表现为腿部、面部和生殖器严重淋巴水肿,并伴有肠道淋巴管扩张、各种面部异常及严重智力发育迟缓。一名21岁男性患者因双侧胸腔积液接受检查。体格检查发现双腿和眼睑水肿、阴囊及手术瘢痕肿胀、前额宽阔、面部异常、鼻梁凹陷、内眦赘皮和小颌畸形。因胸腔甘油三酯水平(650mg/dL)诊断为乳糜胸。淋巴闪烁造影显示双下肢淋巴引流延迟。该患者因面部异常、淋巴水肿、癫痫、乳糜胸及轻度智力发育迟缓被诊断为亨内坎综合征。