Abstract
Objective: The present study was aimed at characterizing main lung changes observed in pulmonary Langerhans cell histiocytosis by means of high-resolution computed tomography. Materials and Methods: High resolution computed tomography findings in eight patients with proven disease diagnosed by open lung biopsy, immunohistochemistry studies and/or extrapulmonary manifestations were retrospectively evaluated. Results: Small rounded, thin-walled cystic lesions were observed in the lung of all the patients. Nodules with predominantly peripheral distribution over the lung parenchyma were observed in 75% of the patients. The lesions were diffusely distributed, predominantly in the upper and middle lung fields in all of the cases, but involvement of costophrenic angles was observed in 25% of the patients. Conclusion: Comparative analysis of high resolution computed tomography and chest radiography findings demonstrated that thinwalled cysts and small nodules cannot be satisfactorily evaluated by conventional radiography. Because of its capacity to detect and characterize lung cysts and nodules, high resolution computed tomography increases the probability of diagnosing pulmonary Langerhans cell histiocytosis. © Colégio Brasileiro de Radiologia e Diagnóstico por Imagem.
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Rodrigues, R. S., Capone, D., & Neto, A. L. F. (2011). Achados da tomografia computadorizada de alta resolução na histiocitose de células de langerhans pulmonar. Radiologia Brasileira, 44(4), 225–232. https://doi.org/10.1590/S0100-39842011000400007
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