Herrera M F, Stone E, Deitel M, Asa S L
Department of Surgery, University of Toronto, Ontario, Canada.
Arch Surg. 1992 Jan;127(1):105-8. doi: 10.1001/archsurg.1992.01420010123020.
Pheochromocytomas may produce several vasoactive peptides. We studied a 39-year-old man who presented with paroxysmal flushing and abdominal pain with normal blood pressure. Laboratory and radiologic studies established the diagnosis of right adrenal pheochromocytoma, and histologic and ultrastructural examination showed the tumor to be a typical pheochromocytoma. Tissue culture yielded large quantities of norepinephrine and epinephrine. However, immunohistochemical studies, tissue assays, and in vitro cultures documented production of several peptides, including calcitonin gene-related peptide and vasoactive intestinal polypeptide in tumor cells. The patient has been asymptomatic after tumor resection. Production of multiple peptides by this tumor may account for the flushing and lack of hypertension, despite elevated catecholamine levels in this patient.
嗜铬细胞瘤可能会产生多种血管活性肽。我们研究了一名39岁的男性,他表现为阵发性潮红和腹痛,但血压正常。实验室和影像学检查确诊为右肾上腺嗜铬细胞瘤,组织学和超微结构检查显示该肿瘤为典型的嗜铬细胞瘤。组织培养产生了大量的去甲肾上腺素和肾上腺素。然而,免疫组化研究、组织分析和体外培养证明肿瘤细胞产生了多种肽,包括降钙素基因相关肽和血管活性肠肽。该患者在肿瘤切除后一直无症状。尽管该患者儿茶酚胺水平升高,但该肿瘤产生多种肽可能是导致潮红和无高血压的原因。