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埃勒斯-当洛斯综合征中的肺发育不全和髌骨发育不全。

Lung hypoplasia and patellar agenesis in Ehlers-Danlos syndrome.

机构信息

Department of Anatomy, Midnapur Medical College & Hospital, Vidyasagar Road, Paschim Medinipur, West Bengal 721101, India.

出版信息

Singapore Med J. 2009 Dec;50(12):e415-8.

Abstract

A 22-year-old male patient was admitted with severe cough associated with purulent expectoration, left-sided chest pain and breathlessness. There was a history of recurrent respiratory ailments since childhood. The patient appeared younger than his chronological age. His face and ears were both dysmorphic. Clinically, the patient was diagnosed with Ehlers-Danlos syndrome (EDS). Computed tomography of the thoracic region revealed hypoplasia of the left lung and hyperplasia of the right lung. Both the patellae were absent. However, ultrasonography of his abdomen, echocardiography and other routine blood and urine examination showed no gross abnormalities. Although other respiratory tract abnormalities with EDS are not uncommon, unilateral lung hypoplasia and patellar agenesis in EDS make this case unique.

摘要

一位 22 岁的男性患者因严重咳嗽伴脓性痰、左侧胸痛和呼吸困难入院。他从小就有反复呼吸道疾病的病史。该患者看起来比实际年龄年轻。他的脸和耳朵都有畸形。临床诊断为埃勒斯-当洛斯综合征(EDS)。胸部区域的计算机断层扫描显示左肺发育不良,右肺过度增生。双侧髌骨缺失。然而,腹部超声、超声心动图和其他常规血液和尿液检查均未显示明显异常。尽管 EDS 还存在其他呼吸道异常,但单侧肺发育不良和髌骨缺失在 EDS 中较为罕见。

相似文献

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Rare pulmonary manifestation of Ehlers-Danlos syndrome.埃勒斯-当洛综合征的罕见肺部表现。
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