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良性和恶性甲状腺组织在卵巢畸胎瘤中的表达以及 BRAF 阳性滤泡状甲状腺乳头状癌的多模态管理的重要性。

Expression of benign and malignant thyroid tissue in ovarian teratomas and the importance of multimodal management as illustrated by a BRAF-positive follicular variant of papillary thyroid cancer.

机构信息

Program in Reproductive and Adult Endocrinology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institute of Diabetes, Digestive, and Kidney Diseases, NIH, Bethesda, MD 20892-1613, USA.

出版信息

Thyroid. 2010 Sep;20(9):981-7. doi: 10.1089/thy.2009.0458.

Abstract

BACKGROUND

The most common type of ovarian germ cell tumor is the teratoma. Thyroid tissue, both benign and malignant, may be a component of an ovarian teratoma. Here we review this topic and illustrate major features by presenting multimodal management of a patient with BRAF-positive disseminated follicular thyroid cancer arising in an ovarian teratoma.

SUMMARY

Malignant thyroid tissue is often difficult to distinguish from benign thyroid tissue arising in ovarian teratomas. Preoperatively, an elevated thyroglobulin (Tg) level, laboratory or clinical evidence of hyperthyroidism, or ultrasonography appearance of "struma pearl" should prompt referral to oncologist for surgical management of a possibly malignant ovarian teratoma. Postoperatively, tumor tissue should be referred to pathologists experienced with differentiating benign from malignant struma ovarii. Once diagnosed, treatment of this rare condition should be handled by a team of specialists with combined treatment modalities. We cared for woman with disseminated thyroid cancer arising in an ovarian teratoma whose history illustrates the complexity of managing ovarian teratomas with malignant thyroid tissue. At age 33 she had an intraoperative rupture of an ovarian cyst, thought to be struma ovarii. During her next pregnancy, pelvic masses were noted; biopsies revealed well-differentiated papillary thyroid carcinoma, follicular variant. She was euthyroid, but had elevated serum Tg levels. Surgical staging demonstrated widely metastatic intraabdominal dissemination. A thyroidectomy revealed no malignancy. A post-(131)I treatment scan revealed diffuse uptake throughout the abdomen. She then developed abdominal pain and, on computed tomography, was found to have multiple intraabdominal foci of disease. Serum Tg was 264 ng/mL while on L-thyroxine for hypothyroidism and to obtain thyrotropin suppression. A 18 fluorodeoxyglucose positron emission tomography scan showed no pathological uptake. The tumor was found to be BRAF mutation positive (K601E). She underwent extensive secondary debulking and a second course of (131)I with lithium pretreatment. Posttreatment scan revealed diffuse abdominal uptake. Six months posttherapy, the patient is asymptomatic with a serum Tg of 18.1 ng/mL.

CONCLUSIONS

Aggressive multimodal management appears to be the most promising approach for malignant thyroid tissue arising in ovarian teratomas.

摘要

背景

最常见的卵巢生殖细胞肿瘤类型是畸胎瘤。甲状腺组织,无论是良性还是恶性,都可能是卵巢畸胎瘤的组成部分。在这里,我们回顾了这一主题,并通过展示一位患有起源于卵巢畸胎瘤的 BRAF 阳性播散性滤泡状甲状腺癌的患者的多模式管理,说明了主要特征。

总结

恶性甲状腺组织通常很难与卵巢畸胎瘤中出现的良性甲状腺组织区分开来。术前,甲状腺球蛋白(Tg)水平升高、实验室或临床甲状腺功能亢进的证据、或“珍珠状甲状腺肿”的超声表现,应提示转介给肿瘤学家进行可能恶性的卵巢畸胎瘤的手术治疗。术后,应将肿瘤组织转介给有鉴别良性和恶性卵巢甲状腺肿经验的病理学家。一旦确诊,这种罕见疾病的治疗应由具有联合治疗模式的专家团队进行处理。我们治疗了一位患有播散性甲状腺癌的女性,她的病史说明了管理具有恶性甲状腺组织的卵巢畸胎瘤的复杂性。她 33 岁时,卵巢囊肿发生术中破裂,被认为是甲状腺肿。在她的下一次怀孕期间,发现盆腔肿块;活检显示分化良好的乳头状甲状腺癌,滤泡状变体。她甲状腺功能正常,但血清 Tg 水平升高。手术分期显示广泛的腹腔内转移。甲状腺切除术显示无恶性肿瘤。(131)I 治疗后扫描显示整个腹部弥漫性摄取。然后她出现腹痛,计算机断层扫描发现多个腹腔内病灶。甲状腺球蛋白在左旋甲状腺素治疗甲状腺功能减退和获得促甲状腺激素抑制时为 264ng/ml。18 氟脱氧葡萄糖正电子发射断层扫描显示无病理性摄取。肿瘤被发现 BRAF 突变阳性(K601E)。她接受了广泛的二次减瘤和第二次(131)I 治疗,并用锂预处理。治疗后扫描显示弥漫性腹部摄取。治疗后 6 个月,患者无症状,血清 Tg 为 18.1ng/ml。

结论

对于起源于卵巢畸胎瘤的恶性甲状腺组织,积极的多模式管理似乎是最有希望的方法。

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