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疑似硬化性间质瘤的幼年型颗粒细胞瘤一例报道并文献复习

王沛丽 丁楠 董驰 王芳

临床与病理杂志Issue(1):94-98,5.
临床与病理杂志Issue(1):94-98,5.DOI:10.3978/j.issn.2095-6959.2016.01.018

疑似硬化性间质瘤的幼年型颗粒细胞瘤一例报道并文献复习

Suspected juvenile granulosa cell tumor of scleroring stromal tumor:report of one case and literature review

王沛丽 1丁楠 2董驰 3王芳2

作者信息

  • 1. 甘肃省监狱管理局兰州医院,兰州大学第二医院康泰分院,兰州 730000
  • 2. 兰州大学第二医院生殖医学中心 兰州 730000
  • 3. 兰州大学第二医院病理科 兰州 730000
  • 折叠

摘要

Abstract

Objective: To discuss clinical and pathological characteristics of the ovarian juvenile granulosa cell tumor. Methods: 1 case in our hospital with suspected juvenile granulosa cell tumor of scleroring stromal tumor was reported and literatures were reviewed.Results: Female, 19-year-old, lower abdominal pain more than 2 months, B ultrasound, MRI and tumor markers all suggested that it was the benign ovarian tumor. An ovarian tumor was found in the right side of ovary and the size is 4 cm × 3 cm × 2 cm. Atfer cutting the surface, it was typically solid with cysts formed. hTe histopathological changes displayed solid lfakes, nodular arrangement. hTe tumor cells were round or oral, cytoplasm stained pink. Nuclear grooves were occasionally conspicuous and mitosis ifgures could be found. Some areas tumor cells were luteinized obvious. hTe immunohistochemical revealed that inhibin-α, CD99, Vimentin, S-100, SMA were all positive. We followed up the patient for 12 months, menstruation was returned to normal and no tumor recurrence.Conclusion: Ovarian juvenile granulosa cell tumor is a rare tumor and researcher should pay enough attention to its clinical pathological features.

关键词

卵巢肿瘤/幼年型颗粒细胞瘤/硬化性间质瘤/病例报道/文献复习

Key words

ovarian tumor/juvenile granulosa cell tumor/sclerosing stromal tumor/case report/literature review

引用本文复制引用

王沛丽,丁楠,董驰,王芳..疑似硬化性间质瘤的幼年型颗粒细胞瘤一例报道并文献复习[J].临床与病理杂志,2016,(1):94-98,5.

基金项目

国家自然科学基金(81202959)。Tis work was supported by National Natural Science Foundation of China (81202959) (81202959)

临床与病理杂志

OACSTPCD

1673-2588

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