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一名患有起源于囊性畸胎瘤的卵巢骨肉瘤的青少年。

An adolescent with ovarian osteosarcoma arising in a cystic teratoma.

作者信息

Aygun Banu, Kimpo Miriam, Lee Thomas, Valderrama Elsa, Leonidas John, Karayalcin Gungor

机构信息

Division of Pediatric Hematology/Oncology and Stem Cell Transplantation, Schneider Children's Hospital, Albert Einstein College of Medicine, New Hyde Park, NY 11020, USA.

出版信息

J Pediatr Hematol Oncol. 2003 May;25(5):410-3. doi: 10.1097/00043426-200305000-00012.

Abstract

A 14-year-old girl had an abdominal mass with the characteristics of an ovarian germ cell tumor on computed tomography scan. The mass, arising from the left ovary, was completely resected and found to be osteosarcoma arising from a mature cystic teratoma. A metastatic lesion in the abdomen did not respond to 2 courses of cisplatin, doxorubicin, ifosfamide, and high-dose methotrexate, and was resected. Seven months after completion of chemotherapy, there were simultaneous local recurrence and lung metastases. Previously, 10 cases of ovarian osteosarcoma have been reported in the literature: 5 were primary osteosarcoma of the ovary, 4 were associated with teratomas, and 1 was part of a malignant mixed mesodermal tumor of the ovary. Of the 10, there are only 2 long-term survivors, both of whom were treated with adjuvant chemotherapy following complete resection.

摘要

一名14岁女孩在计算机断层扫描中发现腹部有一个具有卵巢生殖细胞肿瘤特征的肿块。该肿块起源于左卵巢,已被完全切除,结果发现是源自成熟囊性畸胎瘤的骨肉瘤。腹部的一个转移病灶对两疗程的顺铂、阿霉素、异环磷酰胺和大剂量甲氨蝶呤无反应,随后被切除。化疗结束七个月后,出现了局部复发和肺转移。此前,文献中已报道10例卵巢骨肉瘤病例:5例为卵巢原发性骨肉瘤,4例与畸胎瘤相关,1例是卵巢恶性混合中胚层肿瘤的一部分。在这10例中,只有2例长期存活者,两人均在完全切除后接受了辅助化疗。

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