1. Interleukin-6 secreting phaeochromocytoma associated with clinical markers of inflammation.
- Author
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Takagi M, Egawa T, Motomura T, Sakuma-Mochizuki J, Nishimoto N, Kasayama S, Hayashi S, Koga M, Yoshizaki K, Yoshioka T, Okuyama A, and Kishimoto T
- Subjects
- Adrenal Gland Neoplasms immunology, Adrenal Gland Neoplasms surgery, Aged, Female, Fever blood, Fever immunology, Humans, Hypertension blood, Hypertension immunology, Immunohistochemistry, Interleukin-6 analysis, Interleukin-6 blood, Neoplasm Proteins analysis, Neoplasm Proteins blood, Pheochromocytoma immunology, Pheochromocytoma surgery, Adrenal Gland Neoplasms metabolism, Interleukin-6 metabolism, Neoplasm Proteins metabolism, Pheochromocytoma metabolism
- Abstract
Phaeochromocytomas have been shown to produce not only catecholamines but other neuropeptides and hormones, with a variety of clinical manifestations. We report a 70-year-old female patient with phaeochromocytoma exhibiting sustained hypertension, low-grade fever, thrombocytosis, and elevated levels of plasma fibrinogen and C-reactive protein. Serum interleukin (IL)-6 levels were significantly elevated, whereas serum IL-1 alpha and IL-1 beta were not detectable. After surgical removal of the tumour, hypertension and low-grade fever disappeared, and the laboratory finding including serum IL-6 concentrations became normal. Immunohistochemical study of the tumour showed positive staining for IL-6. Culture of the resected tumour revealed the production of large amounts of IL-6. It is suggested that IL-6 secreted by the tumour was responsible for some of the clinical manifestations in this patient.
- Published
- 1997
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