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Catamenial pneumothorax revealing diaphragmatic endometriosis: a case report and revue of literature

机译:揭露diaphragm肌子宫内膜异位症的前瞻性气胸:一例报告并文献复习

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摘要

Catamenial pneumothorax (CP) is a rare entity of spontaneous, recurring pneumothorax in women. We aim to discuss the etiology, clinical course, and surgical treatment of a 42-year-old woman with CP. This patient had a right-sided spontaneous pneumothoraces occurred one week after menses. She had under-gone video-assisted thoracoscopic surgery (VATS) because of a persistent air leak under chest tube. VATS revealed multiple diaphragmatic fenestrations with an upper right nodule. Defects were removed and a large part of the diaphragm was resected. Pleural abrasion was then performed over the diaphragm. Diaphragmatic endometriosis was confirmed by microscopic examination. Medical treatment with GnRH agonists was prescribed, and after recovery, the patient has been symptoms free for 20 months.
机译:在女性中,Catamenial气胸(CP)是一种罕见的自发性复发性气胸。我们的目的是讨论一名42岁的CP患者的病因,临床过程和手术治疗。该患者在月经后一周出现一次右侧自发性气胸。由于胸管下持续漏气,她进行了电视胸腔镜手术(VATS)。 VATS显示多个multiple肌窗孔,右上结节。去除缺陷,切除大部分隔膜。然后在隔膜上进行胸膜磨蚀。通过显微镜检查证实metri肌子宫内膜异位。处方了GnRH激动剂的药物治疗,康复后,患者20个月无症状。

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