Paláu Mauricio A, Merino Maria J, Quezado Martha
Laboratory of Pathology, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Hum Pathol. 2006 May;37(5):623-6. doi: 10.1016/j.humpath.2005.12.006. Epub 2006 Mar 13.
Gangliocytic paraganglioma (GP) is an unusual tumor in the wide spectrum of neuroendocrine neoplasms. The biologic behavior and histogenesis of this tumor is uncertain because, despite its benign histologic features, there have been reports of metastases to regional lymph nodes and distant metastases. Although most of these tumors have been reported in the duodenum, examples of GP arising in extra-ampullary sites have been well documented. Herein, we report the case of a lung GP corticotropin producing and presenting as Cushing's syndrome. After removal of the tumor, there was a significant drop in cortisol and corticotropin levels. To our knowledge, this is the first report of a GP causing Cushing's syndrome.
神经节细胞副神经节瘤(GP)是广泛的神经内分泌肿瘤谱中一种不常见的肿瘤。该肿瘤的生物学行为和组织发生尚不确定,因为尽管其组织学特征为良性,但已有区域淋巴结转移和远处转移的报道。虽然大多数此类肿瘤报道位于十二指肠,但发生于壶腹外部位的GP病例已有充分记录。在此,我们报告一例产生促肾上腺皮质激素并表现为库欣综合征的肺GP病例。肿瘤切除后,皮质醇和促肾上腺皮质激素水平显著下降。据我们所知,这是关于GP导致库欣综合征的首例报告。