Lymphangioleiomyomatosis: a radiological diagnosis ================================================== * Lokesh Shahani ## Description Lymphangioleiomyomatosis (LAM) is a rare disease which predominantly affects young females and is commonly found in association with tuberous sclerosis.1 The clinical features result from progressive cystic destruction of the lungs and the accumulation of LAM cells within the lungs and axial lymphatics.2 The gold standard for the diagnosis of LAM is a tissue biopsy which shows nodular infiltration by abnormal smooth muscle cells, termed LAM cells. Not all patients with LAM require tissue biopsy for a definitive diagnosis as the disease has a characteristic computerised axial tomography (CAT) appearance in the majority of cases. The author reports a 34-year-old non-smoking African–American female who presented to the clinic with progressive shortness of breath (Figure 1). CAT scan chest showed multiple well-defined thin-walled bilateral lung cysts which are randomly distributed throughout the lungs with normal intervening lung parenchyma consistent with LAM. There were no infiltrates, worrisome nodules, or pleural effusion. LAM needs to be differentiated from other chronic pulmonary diseases which present with a cystic lung appearance. Langerhans cell histiocytosis which closely mimics LAM is predominantly characterised by nodules and cyst walls of variable thickness and tends to spare the basal parts of the lung near the costophrenic angles.3 Centrilobular emphysema can be differentiated from LAM by absence of well-defined walls and the distribution of the vessels relative to the cystic spaces where the vessels can cross cystic spaces.3 ![Figure 1](http://casereports.bmj.com/https://casereports.bmj.com/content/casereports/2012/bcr.11.2011.5192/F1.medium.gif) [Figure 1](http://casereports.bmj.com/content/2012/bcr.11.2011.5192/F1) Figure 1 Computerised axial tomography scan of the chest showing multiple well-defined thin-walled bilateral lung cysts consistent with lymphangioleiomyomatosis. ## Footnotes * Competing interests None. * Patient consent Obtained. ## References 1. Johnson SR. Lymphangioleiomyomatosis. Eur Respir J 2006;27:1056–65. [Abstract/FREE Full Text](http://casereports.bmj.com/lookup/ijlink/YTozOntzOjQ6InBhdGgiO3M6MTQ6Ii9sb29rdXAvaWpsaW5rIjtzOjU6InF1ZXJ5IjthOjQ6e3M6ODoibGlua1R5cGUiO3M6NDoiQUJTVCI7czoxMToiam91cm5hbENvZGUiO3M6MzoiZXJqIjtzOjU6InJlc2lkIjtzOjk6IjI3LzUvMTA1NiI7czo0OiJhdG9tIjtzOjM5OiIvY2FzZXJlcG9ydHMvMjAxMi9iY3IuMTEuMjAxMS41MTkyLmF0b20iO31zOjg6ImZyYWdtZW50IjtzOjA6IiI7fQ==) 2. Johnson SR, Tattersfield AE. Decline in lung function in lymphangioleiomyomatosis: relation to menopause and progesterone treatment. Am J Respir Crit Care Med 1999;160:628–33. [CrossRef](http://casereports.bmj.com/lookup/external-ref?access_num=10.1164/ajrccm.160.2.9901027&link_type=DOI) [PubMed](http://casereports.bmj.com/lookup/external-ref?access_num=10430739&link_type=MED&atom=%2Fcasereports%2F2012%2Fbcr.11.2011.5192.atom) [Web of Science](http://casereports.bmj.com/lookup/external-ref?access_num=000081947700039&link_type=ISI) 3. Seaman DM, Meyer CA, Gilman MD, et al. Diffuse cystic lung disease at high-resolution CT. AJR Am J Roentgenol 2011;196:1305–11. [CrossRef](http://casereports.bmj.com/lookup/external-ref?access_num=10.2214/AJR.10.4420&link_type=DOI) [PubMed](http://casereports.bmj.com/lookup/external-ref?access_num=21606293&link_type=MED&atom=%2Fcasereports%2F2012%2Fbcr.11.2011.5192.atom) [Web of Science](http://casereports.bmj.com/lookup/external-ref?access_num=000290854000044&link_type=ISI)