Dhingra Kajal Kiran, Jain Parul, Garg Ankur, Khurana Nita
Maulana Azad Medical College and Lok Nayak Hospital, Bahadur Shah Zafar Marg, New Delhi, India.
Int J Gynecol Pathol. 2009 May;28(3):231-3. doi: 10.1097/PGP.0b013e31818e531b.
Struma ovarii is a highly specialized and rare form of mature teratomas constituting 2% of all teratomas although small foci of thyroid tissue may be found in 5% to 15% of teratomas. Coexistence of this unusual germ cell tumor with ovarian epithelial tumors has been reported rarely; however, concomitant struma ovarii and serous cystadenofibroma has been mentioned in only 1 case report in the extensively searched medical literature. We report a rare occurrence of struma ovarii along with a serous cystadenofibroma in a 47-year-old woman.
卵巢甲状腺肿是成熟畸胎瘤中一种高度特殊且罕见的类型，占所有畸胎瘤的2%，不过在5%至15%的畸胎瘤中可发现小灶性甲状腺组织。这种不寻常的生殖细胞肿瘤与卵巢上皮性肿瘤共存的情况鲜有报道；然而，在广泛检索的医学文献中，仅有1例病例报告提及了卵巢甲状腺肿与浆液性囊腺纤维瘤并存的情况。我们报告了1例47岁女性罕见的卵巢甲状腺肿合并浆液性囊腺纤维瘤病例。
