Hmidi Amira, Sahraoui Ghada, Charfi Lamia, Hassine Abouda, Aloui Haithem, Mrad Karima
Pathology Department, Salah Azaiz Institute, Tunis, Tunisia.
Pathology Department, Salah Azaiz Institute, Tunis, Tunisia.
Int J Surg Case Rep. 2023 Nov;112:108944. doi: 10.1016/j.ijscr.2023.108944. Epub 2023 Oct 13.
Malignant transformation within mature cystic teratomas is a rare occurrence, with an estimated risk ranging from 0.17 % to 2 %. Squamous cell carcinoma is the most common malignancy associated with this condition, while papillary thyroid carcinoma rarely presents within ovarian teratomas. This transformation predominantly affects postmenopausal women but can, albeit rarely, manifest in younger women.
We present a case of a 37-year-old woman who was incidentally found to have a right ovarian cyst measuring 20 × 20 × 10 mm during a cesarean section, displaying characteristic features of a teratoma. Histological examination confirmed the presence of papillary thyroid carcinoma originating within the ovarian mature cystic teratoma. Immunohistochemical analysis demonstrated positive staining for specific thyroid differentiation markers, including TTF1 and Thyroglobulin. The patient was in good health otherwise, with normal clinical and radiological evaluations of the thyroid, and no additional treatment was administered. Currently, seven years after surgery, the patient remains free of recurrence.
DISCUSSION/CONCLUSION: Given the rarity of this condition, established treatment protocols are lacking, and its histogenesis remains uncertain. To advance our understanding of pathogenesis, prognosis, and therapeutic strategies for this malignant transformation, the publication of additional cases with similar presentations would be highly valuable.
成熟性囊性畸胎瘤发生恶性转化较为罕见,估计风险为0.17%至2%。鳞状细胞癌是与此情况相关的最常见恶性肿瘤,而乳头状甲状腺癌很少出现在卵巢畸胎瘤内。这种转化主要影响绝经后女性,但尽管罕见,也可在年轻女性中表现出来。
我们报告一例37岁女性,她在剖宫产时偶然发现右侧卵巢有一个20×20×10mm的囊肿,具有畸胎瘤的特征性表现。组织学检查证实卵巢成熟性囊性畸胎瘤内存在乳头状甲状腺癌。免疫组化分析显示甲状腺特异性分化标志物TTF1和甲状腺球蛋白呈阳性染色。患者其他方面健康,甲状腺临床和影像学评估正常,未进行额外治疗。目前,术后七年,患者无复发。
讨论/结论:鉴于这种情况罕见,缺乏既定的治疗方案,其组织发生仍不确定。为增进我们对这种恶性转化的发病机制、预后和治疗策略的理解,发表更多类似病例报告将非常有价值。