Suzuki K, Miyashita A, Inoue Y, Iki S, Enomoto H, Takahashi Y, Takemura T
Department of Hematology, Japanese Red Cross Medical Center, Tokyo.
Acta Haematol. 1991;85(4):217-9. doi: 10.1159/000204897.
A 42-year-old female with high fever and headache was admitted. Physical examination revealed hypertension, thrombocytosis with megakaryocytosis, hyperfibrinogenemia, and high level of serum noradrenaline. After operation of extramedullary pheochromocytoma, all symptoms disappeared and findings became normal. The supernatant of tumor culture showed high levels of interleukin-6.
一名42岁高热、头痛的女性入院。体格检查发现高血压、血小板增多伴巨核细胞增多、纤维蛋白原血症及血清去甲肾上腺素水平升高。髓外嗜铬细胞瘤手术后,所有症状消失,检查结果恢复正常。肿瘤培养上清液显示白细胞介素-6水平升高。