Malignant struma ovarii: a case report |
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| Authors: | Bolat F Erkanli S Kayaselcuk F Aslan E Tuncer I |
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| Institution: | 1. Department of Pathology, Ba?kent University Faculty of Medicine, Adana Teaching and Medical Research Center, Adana, Turkey;2. Department of Gynecology and Obstetric, Ba?kent University Faculty of Medicine, Adana Teaching and Medical Research Center, Adana, Turkey;1. Department of Chemistry, Jayaprakash Narayan College of Engineering, Mahabubnagar 509001, Andhra Pradesh, India;2. Department of Physics, Nizam College, Basheerbagh Osmania University, Hyderabad 500001, Andhra Pradesh, India;3. Department of Chemistry, Osmania University, Hyderabad 500007, Andhra Pradesh, India;1. Royal Children''s Hospital, Department of Paediatric Urology, Melbourne, Australia;2. Paediatric Surgery Department, University Hospital, Poitiers, France;3. FD Stephens Surgical Research Group, Murdoch Children''s Research Institute, Melbourne, Australia;4. Department of Paediatrics, University of Melbourne, Melbourne, Australia;1. Department of Physics, The Islamia University of Bahawalpur, Bahawalpur 63100, Pakistan;2. Department of Chemistry, The Islamia University of Bahawalpur, Bahawalpur 63100, Pakistan;3. Deanship of Scientific Research, College of Engineering, King Saud University, P.O. Box 800, Riyadh 11421, Saudi Arabia;4. Materials Science and Engineering Division, King Abdullah University of Science and Technology, Thuwal 23955-6900, Kingdom of Saudi Arabia;1. Physics Department, Faculty of Science, Alexandria University, Alexandria 21511, Egypt;2. Chemistry Department, Faculty of Science, Minia University, El-Minia 61519, Egypt |
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| Abstract: | Malignant struma ovarii is a rare form of the ovarian germ cell tumors. Hence, diagnosis and management of malignant struma ovarii have not been clearly defined. We present the case of a 34-year-old woman with papillary carcinoma arising in struma ovarii. The malignant component of this tumor was detected after laparoscopic removal, and a re-staging operation was performed afterwards. There was no evidence of clinical malignancy or metastases. In this paper, clinical features, treatment guidelines, diagnostic features, and immunohistochemical characteristics of this tumor are reviewed. |
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