Sivak E D, Ahmad M, Hanson M R, Mitsumoto H, Wilbourn A J
South Med J. 1987 Feb;80(2):205-8. doi: 10.1097/00007611-198702000-00016.
Although the adult form of acid maltase deficiency is characterized by weakness of the limb girdle muscles, weakness of the respiratory muscles out of proportion to that of the limb muscles may make the diagnosis less obvious. We present four patients aged 35 to 57 with respiratory muscle weakness associated with signs of cor pulmonale and symptoms of alveolar hypoventilation. Each had symptoms of fatigue, hypersomnolence, morning headache, and orthopnea, the cause of which was misdiagnosed. The key to diagnosis was paradoxic abdominal motion on inspiration. This finding, consistent with diaphragmatic paralysis, led to neurologic evaluation, electromyographic examination, and muscle biopsy to confirm the diagnosis. The symptoms of alveolar hypoventilation were reversed with chronic nocturnal ventilation, which assisted in rehabilitating some patients.
尽管成人型酸性麦芽糖酶缺乏症的特征是肢带肌无力,但呼吸肌无力程度与肢体肌肉不成比例可能会使诊断不那么明显。我们报告了4例年龄在35至57岁之间的患者,他们存在呼吸肌无力,并伴有肺心病体征和肺泡通气不足症状。每个人都有疲劳、嗜睡、晨起头痛和端坐呼吸症状,这些症状的病因被误诊。诊断的关键是吸气时出现反常腹部运动。这一发现与膈肌麻痹一致,进而进行了神经学评估、肌电图检查和肌肉活检以确诊。慢性夜间通气可逆转肺泡通气不足的症状,有助于部分患者康复。