[血管性水肿样体型的罕见病因]
[A Rare Cause of an Angioedema-Like Habitus].
作者信息
Hayoz Christelle, Rickenbacher-Frey Sarah, Ernst Susanne
机构信息
1 Interdisziplinäre Notfallstation, Kantonsspital Olten.
出版信息
Praxis (Bern 1994). 2018 Jul;107(14):773-776. doi: 10.1024/1661-8157/a003017.
A Rare Cause of an Angioedema-Like Habitus Abstract. We report about a 69-year-old patient arriving at the emergency room with suspected allergic reaction grade III due to a pronounced facial swelling, dyspnea and dizziness. However, the cause was a bilateral pneumothorax with massive soft-tissue emphysema. On the one side it was due to a spontaneous secondary genesis in the context of a chronic pulmonary disease, on the other side it was due to a traumatic serial rib fracture.
类血管性水肿样表现的罕见病因 摘要。我们报告了一名69岁的患者，因面部明显肿胀、呼吸困难和头晕被送往急诊室，怀疑为III级过敏反应。然而，病因是双侧气胸伴大量软组织气肿。一侧是慢性肺部疾病背景下的自发性继发性发病，另一侧是外伤性多发性肋骨骨折所致。
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