腹膜和淋巴结胶质瘤病合并子宫内膜异位症,并伴有卵巢未成熟畸胎瘤:一个病例研究和文献复习。

Korean Journal of Pathology Pub Date : 2013-12-01 Epub Date: 2013-12-24 DOI:10.4132/KoreanJPathol.2013.47.6.587
Na Rae Kim, Soyi Lim, Juhyeon Jeong, Hyun Yee Cho
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引用次数: 13

摘要

腹膜胶质瘤病(GP)是指成熟神经胶质组织植入腹膜,通常伴有卵巢成熟或未成熟畸胎瘤。在此,我们报告一例卵巢未成熟畸胎瘤合并胶质瘤病累及腹膜、淋巴结和道格拉斯袋,胶质瘤病与子宫内膜异位症共存。据我们所知,仅有7例GP与子宫内膜异位症共存。8例成熟的胶质组织在淋巴结,即淋巴结胶质瘤病,已发表或与GP相关或无。多能性体腔干细胞的化生被认为是子宫内膜异位症和GP的发病机制,而不是成熟程度不同的卵巢畸胎瘤的植入转移。这一理论也适用于GP独立于卵巢畸胎瘤肿瘤。据我们所知,结节性胶质瘤病与GP共存,并涉及子宫内膜异位症尚未报道。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Peritoneal and nodal gliomatosis with endometriosis, accompanied with ovarian immature teratoma: a case study and literature review.

Gliomatosis peritonei (GP) indicates the peritoneal implantation of mature neuroglial tissue and is usually accompanied by ovarian mature or immature teratoma. Here, we report a case of ovarian immature teratoma associated with gliomatosis involving the peritoneum, lymph nodes and Douglas' pouch, where gliomatosis coexisted with endometriosis. As far as we know, only seven cases of GP have been reported as coexisting with endometriosis. Eight cases with mature glial tissue in the lymph nodes, i.e., nodal gliomatosis, have been published either in association with GP or in its absence. Metaplasia of pluripotent coelomic stem cells has been suggested to be responsible for the pathogenesis of endometriosis and GP rather than implantation metastases of ovarian teratomatous tumor with varying maturation. This theory is also applied to GP independently of ovarian teratomatous tumors. To the best of our knowledge, nodal gliomatosis coexisting with GP and also involving endometriosis has not yet been reported.

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来源期刊
Korean Journal of Pathology
Korean Journal of Pathology 医学-病理学
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6-12 weeks
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