Pheochromocytoma associated with ectopic ACTH-producing tumor and hyper-interleukin-6emia: a case report with review of literature.

IF 1.3 4区 医学 Q4 ENDOCRINOLOGY & METABOLISM
Hironori Nakahira, Shozo Miyauchi, Kyoko Watanabe, Kazuyuki Akesaka, Keizo Ono, Osamu Ebisui, Teruki Miyake, Shinya Furukawa, Yoichi Hiasa, Bunzo Matsuura
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引用次数: 0

Abstract

Pheochromocytomas occur in the adrenal medulla and present with various symptoms associated with excessive catecholamine production. Although pheochromocytomas associated with ectopic ACTH-producing tumors and hyper-interleukin-6emia (hyper-IL-6emia) have been reported, those associated with both diseases simultaneously have not been reported. In pheochromocytomas with ectopic ACTH-producing tumors and hyper-IL-6emia, the disease characteristics and relationship between each hormone and cytokine are unknown. Herein, we report a case of a 56-year-old woman with stroke whose computed tomography scans of the abdomen revealed a right adrenal tumor on systemic examination. Endocrinological examination revealed elevated plasma levels of catecholamines and their metabolites in the urine and elevated levels of plasma ACTH, serum cortisol, and serum dehydroepiandrosterone sulfate, leading to a diagnosis of right pheochromocytoma and associated ectopic ACTH-producing tumor. Furthermore, hyper-IL-6emia was detected as a key indicator of anemia due to inflammatory hematopoietic disorders. The patient's general condition improved with drug therapy, including 1,000 mg/d of metyrapone, 2 mg/h of phentolamine, 8 mg/d of doxazosin, and systemic management. Dexamethasone suppression tests demonstrated suppressed serum cortisol and IL-6 levels, and dexamethasone dose-dependently increased plasma adrenaline and noradrenaline levels. These findings indicate that excess glucocorticoids play a stimulatory role in catecholamine secretion and a concentration-suppressive role in serum IL-6 levels in pheochromocytomas associated with ectopic ACTH-producing tumors and hyper-IL-6emia. The presence of rare comorbidities should be considered if the clinical findings cannot be explained by the pathophysiology of a pheochromocytoma alone because pheochromocytomas can be associated with the production of other hormones and cytokines.

嗜铬细胞瘤伴异位acth生成瘤和高白细胞介素-6血症1例并文献复习。
嗜铬细胞瘤发生于肾上腺髓质,呈现与过量儿茶酚胺产生相关的各种症状。虽然嗜铬细胞瘤与异位acth产生肿瘤和高白细胞介素-6血症(高il -6血症)相关已被报道,但与这两种疾病同时相关的未见报道。异位acth产生肿瘤伴高il -6血症的嗜铬细胞瘤,疾病特点及各激素和细胞因子之间的关系尚不清楚。在此,我们报告一个56岁女性中风的病例,其腹部电脑断层扫描在全身检查中显示右侧肾上腺肿瘤。内分泌检查显示尿中儿茶酚胺及其代谢物血浆水平升高,血浆ACTH、血清皮质醇、血清硫酸脱氢表雄酮水平升高,诊断为右侧嗜铬细胞瘤及相关异位ACTH生成肿瘤。此外,高il -6血症被检测为炎症性造血障碍引起的贫血的关键指标。经药物治疗,患者一般情况好转,包括1000mg /d的美替拉酮,2mg /h的酚妥拉明,8mg /d的多沙唑嗪和全身管理。地塞米松抑制试验显示血清皮质醇和IL-6水平受到抑制,地塞米松剂量依赖性地增加血浆肾上腺素和去甲肾上腺素水平。这些发现表明,过量的糖皮质激素在与异位acth产生肿瘤和高IL-6血症相关的嗜铬细胞瘤中发挥儿茶酚胺分泌的刺激作用和血清IL-6水平的浓度抑制作用。如果临床表现不能单独用嗜铬细胞瘤的病理生理来解释,则应考虑罕见合并症的存在,因为嗜铬细胞瘤可能与其他激素和细胞因子的产生有关。
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来源期刊
Endocrine journal
Endocrine journal 医学-内分泌学与代谢
CiteScore
4.30
自引率
5.00%
发文量
224
审稿时长
1.5 months
期刊介绍: Endocrine Journal is an open access, peer-reviewed online journal with a long history. This journal publishes peer-reviewed research articles in multifaceted fields of basic, translational and clinical endocrinology. Endocrine Journal provides a chance to exchange your ideas, concepts and scientific observations in any area of recent endocrinology. Manuscripts may be submitted as Original Articles, Notes, Rapid Communications or Review Articles. We have a rapid reviewing and editorial decision system and pay a special attention to our quick, truly scientific and frequently-citable publication. Please go through the link for author guideline.
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