Márk Z, Sápi Z, Mészáros Z, Strausz J
Fóvárosi Onkormányzat Szent János Kórház, Budapest.
Orv Hetil. 2001 Aug 26;142(34):1851-4.
This is a case history of a 24-year-old female patient in whom two rare pulmonary diseases occurred: Langerhans cell histiocytosis and four years later lymphangioleiomyomatosis were diagnosed. Both diseases were verified by the examination of the lung tissue removed by the surgery for pneumothorax. The patient's symptoms were characterised by coughing, dyspnoe, repeated pneumothorax. The authors summarised the characteristics and treatment of these diseases. This case history is worth of reporting for its unique rareness.
这是一名24岁女性患者的病例史,该患者出现了两种罕见的肺部疾病:朗格汉斯细胞组织细胞增多症,四年后又被诊断出淋巴管平滑肌瘤病。这两种疾病均通过因气胸进行手术切除的肺组织检查得以确诊。患者的症状表现为咳嗽、呼吸困难、反复气胸。作者总结了这些疾病的特点及治疗方法。该病例史因其独特的罕见性而值得报道。