Pulmonary Lymphangiomyomatosis Associated with Renal and Hepatic Angiomyolipoma Mass in a Patient with Tuberous Sclerosis Complex

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摘要To the Editor:Tuberous sclerosis complex (TSC),a rare autosomal dominant and variable penetrance,affects about 10 in every 100,000 people.[1] In general,it is described as a clinical triad of adenomas,mental disorders,and seizures.However,due to incomplete penetrance,symptoms may be involved in isolated organs,which may manifest as mild incomplete diseases or involve multiple organs.Pulmonary lymphangiomyomatosis (LAM) associated with both renal and hepatic angiomyolipomas (AMLs) in a TSC patient is very rare.To the best of our knowledge,only one case has been reported by Ciftci et al.[2] Here,we present such a case with clinical and pathological analysis.

作者单位 Department of Pathology, Taizhou Central Hospital(Taizhou University Hospital), Taizhou, Zhejiang 318000, China ^[1] Department of Pathology, Taizhou Hospital of Taizhou Enze Medical Group, Linhai, Zhejiang 317000, China ^[2]

栏目名称

Correspondence

DOI 10.4103/0366-6999.220310

发布时间 2018-01-15

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准确一般字义偏差语意偏离译文作用小提交