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1 Introduction Lymphangioleiomyomatosis (LAM) is a rare disease affecting women of childbearing age. LAM primarily manifests as diffuse pulmonary cysts in the lungs, with the proliferation of smooth muscle cell-like LAM cells in lymphatic tissues and kidneys. The main symptoms of LAM are respiratory complications, including dyspnea and recurrent pneumothorax; other symptoms include renal angiomyolipoma and chylothorax [1, 2].
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