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卡尼三联征中胃肿瘤的有趣特性。超微结构和免疫组化观察。

The intriguing nature of gastric tumors in Carney's triad. Ultrastructural and immunohistochemical observations.

作者信息

Blei E, Gonzalez-Crussi F

机构信息

Department of Pathology, Children's Memorial Hospital, Chicago, Illinois 60614.

出版信息

Cancer. 1992 Jan 15;69(2):292-300. doi: 10.1002/1097-0142(19920115)69:2<292::aid-cncr2820690204>3.0.co;2-j.

Abstract

The authors describe clinical and pathologic features present in an adolescent girl who had a gastric tumor and mediastinal mass. The latter was shown to be a paraganglioma, and the gastric neoplasm was classified as malignant "leiomyoblastoma," with the use of current histologic criteria. This tumor had metastasized to the liver but not to the lungs. Although the histologic criteria for leiomyoblastoma were fulfilled, no definite evidence of smooth-muscle cell differentiation was present ultrastructurally or by immunostaining methods. Gastric tumors that form part of "Carney's triad" are known to differ clinically and pathologically in important ways from smooth-muscle cell malignant neoplasms that are not part of this syndrome. Some have been classified as gastrointestinal autonomic nerve tumors, but the current study did not confirm this contention. The nature of gastric leiomyoblastomas in Carney's multitumoral association remains undecided.

摘要

作者描述了一名患有胃肿瘤和纵隔肿块的青春期女孩的临床和病理特征。后者被证实为副神经节瘤,而胃肿瘤根据当前的组织学标准被归类为恶性“平滑肌瘤母细胞瘤”。该肿瘤已转移至肝脏,但未转移至肺部。尽管满足了平滑肌瘤母细胞瘤的组织学标准,但在超微结构或免疫染色方法上均未发现平滑肌细胞分化的确切证据。已知构成“卡尼三联征”一部分的胃肿瘤在临床和病理上与不属于该综合征的平滑肌细胞恶性肿瘤有重要差异。一些已被归类为胃肠道自主神经肿瘤,但当前的研究并未证实这一观点。卡尼多肿瘤关联中胃平滑肌瘤母细胞瘤的性质仍未确定。

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