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卵巢原发性神经外胚层肿瘤。25例报告。

Primary neuroectodermal tumors of the ovary. A report of 25 cases.

作者信息

Kleinman G M, Young R H, Scully R E

机构信息

Department of Pathology, Harvard Medical School, Boston, Massachusetts.

出版信息

Am J Surg Pathol. 1993 Aug;17(8):764-78. doi: 10.1097/00000478-199308000-00002.

Abstract

Twenty-five primary ovarian neuroectodermal tumors occurred in females from 6 to 69 (average, 23) years of age; they had the usual presenting symptoms of abdominal swelling or pain. The tumors, which varied from cystic to solid, ranged from 4 to 20 cm (average, 14 cm) in diameter. Microscopic examination revealed three histologic categories--differentiated, primitive, and anaplastic--with the tumors in the first group having a better prognosis than those in the other two groups. Five of the six differentiated gliomas were pure ependymomas, and one was an ependymoma with an astrocytoma component; none contained teratomatous elements. Two patients with stage I tumors were alive 4 and 5 years postoperatively. The one patient with stage IIA tumor was free of disease at 3 years; one of the two patients with a stage III tumor died of tumor after 5 years, and one had two recurrences but was alive and well at 5 years. Twelve tumors were primitive, resembling medulloepithelioma, ependymoblastoma, neuroblastoma or medulloblastoma. Seven tumors had teratomatous foci of other types, including three dermoid cysts. Three patients with stage I tumors were alive at 7 months, 3 years, and 9 years postoperatively; six of seven patients with stage III tumors died of tumor 2 to 20 months postoperatively, and one was alive with disease at 1 year. Seven tumors were anaplastic, resembling glioblastoma. All contained foci of squamous epithelium. One patient with stage IA tumor died of tumor at 2 years, but two were free of tumor after 3 and 4 years. One patient with a stage IIA tumor died of disease after 5 years; another was alive with tumor at 1 year. One patient with a stage III tumor died after 4 months. The differential diagnosis of neuroectodermal tumors of the ovary includes many primary and metastatic ovarian neoplasms of diverse types, and distinction among them is important. Neuroectodermal tumors should be considered when examining unusual ovarian tumors, particularly if the patient is young.

摘要

25例原发性卵巢神经外胚层肿瘤发生于6至69岁(平均23岁)的女性;患者通常表现为腹部肿胀或疼痛。肿瘤从囊性到实性不等,直径4至20厘米(平均14厘米)。显微镜检查显示有三种组织学类型——分化型、原始型和间变型——第一组肿瘤的预后优于其他两组。6例分化型胶质瘤中有5例为纯室管膜瘤,1例为室管膜瘤伴星形细胞瘤成分;均无畸胎瘤成分。2例I期肿瘤患者术后分别存活4年和5年。1例IIA期肿瘤患者术后3年无疾病;2例III期肿瘤患者中1例术后5年死于肿瘤,另1例复发两次,但术后5年仍存活且状况良好。12例肿瘤为原始型,类似髓上皮瘤、室管膜母细胞瘤、神经母细胞瘤或髓母细胞瘤。7例肿瘤有其他类型的畸胎瘤灶,包括3例皮样囊肿。3例I期肿瘤患者术后分别存活7个月、3年和9年;7例III期肿瘤患者中有6例术后2至20个月死于肿瘤,1例术后1年带瘤存活。7例肿瘤为间变型,类似胶质母细胞瘤。均含有鳞状上皮灶。1例IA期肿瘤患者术后2年死于肿瘤,但2例术后3年和4年无肿瘤。1例IIA期肿瘤患者术后5年死于疾病;另1例术后1年带瘤存活。1例III期肿瘤患者术后4个月死亡。卵巢神经外胚层肿瘤的鉴别诊断包括许多不同类型的原发性和转移性卵巢肿瘤,区分它们很重要。检查不寻常的卵巢肿瘤时应考虑神经外胚层肿瘤,尤其是患者年轻的时候。

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