Minetto M, Dovio A, Ventura M, Cappia S, Daffara F, Terzolo M, Angeli A
Department of clinical and Biological Sciences, General Medical Clinic, San Luigi Hospital, Orbassano (TO), Italy.
J Endocrinol Invest. 2003 May;26(5):453-7. doi: 10.1007/BF03345202.
Pheochromocytomas are tumors able to produce catecholamines and a variety of biologically active neuropeptides. We report the case of a 36-yr-old female patient with pheochromocytoma exhibiting headache, intermittent fever, thrombocytosis, and marked inflammatory signs. Nonsteroidal anti-inflammatory drugs were ineffective in lowering the body temperature, while a corticosteroid agent obtained excellent results. IL-6 was found elevated (20 pg/ml); it fell to 4.5 pg/ml 3 weeks after the adrenalectomy, in parallel to normalization of other laboratory data. The interleukin-6 (IL-6) over-production can either be ascribed directly to the tumor (as confirmed by immunohistochemistry) or indirectly accounted for by tumoral production, as a consequence of the high levels of circulating norepinephrine. To our knowledge, our paper represents the 6th case report of IL-6 secreting pheochromocytoma associated with clinical markers of inflammatory response.
嗜铬细胞瘤是能够产生儿茶酚胺和多种生物活性神经肽的肿瘤。我们报告了一例36岁患有嗜铬细胞瘤的女性患者,该患者表现出头痛、间歇性发热、血小板增多症和明显的炎症体征。非甾体抗炎药在降低体温方面无效,而一种皮质类固醇药物取得了极佳效果。发现白细胞介素-6(IL-6)升高(20 pg/ml);肾上腺切除术后3周,其降至4.5 pg/ml,与此同时其他实验室数据恢复正常。白细胞介素-6(IL-6)的过度产生要么直接归因于肿瘤(免疫组织化学证实),要么间接由肿瘤产生导致,这是循环中去甲肾上腺素水平升高的结果。据我们所知,我们的论文是第6例关于分泌IL-6的嗜铬细胞瘤与炎症反应临床标志物相关的病例报告。