Corrigendum to ’Dual malignancy in young lady in the sitting of Cowden syndrome: Case report and review of the literature’ [Eur J Surg Oncol 47/2 (2021) e47]

The authors regret that Dr. Majsi Alzahrani was left of the author list on original article. contributed heavily as co-other in publishing this work. would like to apologise for any inconvenience caused. Dual malignancy young lady sitting Cowden syndrome : Case report and review literatureEuropean Journal Surgical OncologyVol. 47Issue 2PreviewBackground: Syndrome (CS) is a rare congenital autosomal dominant disorder affects around 1/200,000 patients with an incomplete penetrance variable expressivity. It presents spectrum disorders due alterations tumor suppressor gene (PTEN). PTEN hamartoma characterized by unique phenotypic features including multiple hamartomas, mucocutaneous lesions which are almost always present, some other typical involving organs; namely thyroid, colon, brain. Full-Text PDF