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[Metastasis surgery in granulosa cell tumor--determining indications and tumor after care].

作者信息

Belz J, Wakker R, Hoepffner J, Caselitz J

机构信息

I. Chirurgische Abteilung, Allgemeines Krankenhaus Hamburg-Altona, BRD.

出版信息

Langenbecks Arch Chir. 1992;377(1):25-7. doi: 10.1007/BF00186145.

DOI:10.1007/BF00186145
PMID:1569801
Abstract

The granulosa cell tumour is a rare and malignant neoplasia of the ovary. As it has a low grade of malignancy a long course of the disease is observed. Following surgical resection, life-long tumour follow-up is recommended. Based on a case report and a review of the literature, the possible sites of metastases are demonstrated. This paper presents the latest therapeutic concepts and discusses the usefulness of metastasis resection.

摘要

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本文引用的文献

1
Combination chemotherapy of ovarian granulosa cell tumor with cis-platinum and doxorubicin.顺铂和阿霉素联合化疗卵巢颗粒细胞瘤
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Recurrent granulosa cell tumour of the ovary 22 years after primary excision.原发性切除术后22年复发性卵巢颗粒细胞瘤。
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[Clinical aspects and therapy of granulosa cell tumors].[颗粒细胞瘤的临床特征与治疗]
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[Granulosa cell tumor. The results of postoperative irradiation].[颗粒细胞瘤。术后放疗结果]
Dtsch Med Wochenschr. 1984 May 11;109(19):750-2. doi: 10.1055/s-2008-1069268.
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[The significance of clinical and morphological parameters for the prognosis of granulosa cell tumors of the ovaries].
Geburtshilfe Frauenheilkd. 1984 May;44(5):295-9. doi: 10.1055/s-2008-1036661.
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Androgenic granulosa cell tumors of the ovary. A clinicopathologic analysis of 17 cases and review of the literature.
Arch Pathol Lab Med. 1984 Oct;108(10):786-91.
7
Clinicopathologic review of 118 granulosa and 82 theca cell tumors.118例颗粒细胞瘤和82例卵泡膜细胞瘤的临床病理回顾
Obstet Gynecol. 1980 Feb;55(2):231-8.
8
Late recurrence of granulosa cell tumour.颗粒细胞瘤的晚期复发
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9
Fine needle aspiration cytologic features of hepatic metastasis of granulosa cell tumor of the ovary. Differential diagnosis.卵巢颗粒细胞瘤肝转移的细针穿刺细胞学特征。鉴别诊断。
Acta Cytol. 1988 Jul-Aug;32(4):527-32.
10
Juvenile granulosa cell tumor of the ovary in children: a clinical study of 15 cases.
J Clin Oncol. 1988 Jun;6(6):990-5. doi: 10.1200/JCO.1988.6.6.990.