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Pulmonary lymphangitic carcinomatosis is the spread of a tumor to the lungs through the lymphatic system, which is a rare and final manifestation of cancer with a poor prognosis.Its main symptom is gradual and progressive dyspnea.The method of choice for diagnosis is high-resolution CT (HRCT), the most common finding of which is an increase in nodular and irregular septal thickness between the lobules with the formation of a network of dense polygons.Histological findings confirm the diagnosis.Here we present a patient with lymphangitic carcinomatosis in Bushehr, which occurred secondary to pulmonary adenocarcinoma.
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Ghanbari et al. (2022) studied this question.
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