医学
嗜铬粒蛋白A
闪烁照相术
神经内分泌肿瘤
促肾上腺皮质激素
神经内分泌肿瘤
附录
内分泌系统
病理
内科学
免疫组织化学
激素
生物
古生物学
作者
Elżbieta Moszczyńska,Katarzyna Pasternak-Pietrzak,Monika Prokop-Piotrkowska,Anna Śliwińska,Sylwia Szymańska,Mieczysław Szalecki
标识
DOI:10.1515/jpem-2020-0442
摘要
Ectopic adrenocorticotropic syndrome (EAS) causes approximately 10-18% of cases of Cushing's syndrome (CS) in adults, while in children it occurs much less frequently.We report two cases of neuroendocrine tumors (of the thymus and the appendix) in a 12-year-old boy and a 15-year-old girl who presented with the clinical features of CS. Elevated serum cortisol, ACTH, and chromogranin levels were observed in both patients. Diagnoses were made on the basis of a mass in the thymus/appendix region visualized with chest/abdominal CT scan and radiotracer accumulation in scintigraphy in the same areas. Histopathological examinations confirmed the diagnoses of NET.EAS is an extremely rare endocrine disorder. However, it should be taken into consideration in the diagnostic process of every case of ACTH-dependent CS.
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