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首页> 外文期刊>International journal of gynecological pathology: Official journal of the International Society of Gynecological Pathologists >High-grade Sarcoma Masquerading as Growing Teratoma Syndrome After Resection of Ovarian Immature Teratoma: Report of a Case
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High-grade Sarcoma Masquerading as Growing Teratoma Syndrome After Resection of Ovarian Immature Teratoma: Report of a Case

机译:卵巢未成熟畸胎瘤切除术后伪装成严重畸胎瘤的高级肉瘤:一例报告

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摘要

A thorough literature search revealed no previous reports of this entity, and we are the first to describe a case of a high-grade sarcoma arising from a recurrent immature teratoma misdiagnosed as growing teratoma syndrome. The patient was a 23-yr-old female, diagnosed at the age of 20 with a Stage IIIB immature ovarian teratoma. After surgery and chemotherapy, the patient developed multiple liver and pelvic masses that were diagnosed as mature teratomas based on small samples obtained by computed tomography-guided core biopsy. Three years after diagnosis the patient presented with severe respiratory difficulty and following resection, the final pathology revealed multiple tumors with foci of high grade sarcoma compatible with primitive neuroectodermal tumor/extraskeletal Ewing sarcoma based on morphology and immunohistochemistry (CD99~+ , CD56~+). However, on the basis of further immunos-taining and fluorescent in situ hybridization studies negative for rearrangement of EWSR1, the final pathologic diagnosis was high-grade unspecified (undifferentiated) sarcoma. This case illustrates the pitfalls of biopsying 1 site in a patient with recurrence of a heterogeneous tumor such as immature ovarian teratoma, especially when rendering a benign diagnosis such as growing teratoma syndrome. It is of utmost importance to adequately sample large-volume recurrent teratomas, and we suggest biopsying several different sites, to increase the likelihood of detecting a malignant component.
机译:详尽的文献检索没有发现该实体的先前报道,我们是第一个描述因误诊为生长性畸胎瘤综合征而复发的未成熟畸胎瘤引起的高度肉瘤的病例。该患者是一名23岁的女性,在20岁时被诊断为IIIB期未成熟卵巢畸胎瘤。经过手术和化学疗法后,患者出现了多个肝脏和盆腔肿块,这些肿块是通过计算机断层扫描引导的核心活检获得的少量样本诊断为成熟的畸胎瘤。诊断后三年,患者出现严重呼吸困难并切除,最终病理显示,根据形态学和免疫组化(CD99〜+,CD56〜+),发现多发高级别肉瘤病灶与原始神经外胚层肿瘤/骨骼外尤因肉瘤相容。 。然而,根据进一步的免疫染色和荧光原位杂交研究,对EWSR1的重排呈阴性,最终的病理诊断为高度未明确的(未分化的)肉瘤。该病例说明了在异质性肿瘤(例如未成熟的卵巢畸胎瘤)复发的患者中活检1个部位的陷阱,尤其是在做出诸如良性畸胎瘤综合征等良性诊断时。对大量的复发性畸胎瘤进行充分采样至关重要,我们建议对多个不同部位进行活检,以增加检测到恶性成分的可能性。

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