Kojima Y, Sakaguchi M, Hatano T, Yamamoto M
Department of Surgery, Kansai Medical University, Osaka, Japan.
Nihon Geka Gakkai Zasshi. 1988 Apr;89(4):622-6.
A case of pheochromocytoma associated with von Recklinghausen's disease is reported. A 53-year-old man consulted the Department of Dermatology of our hospital because of Dermatoptosis in the breast and abdomen. He asked to resect of the mass. Blood bio chemistry findings were almost within normal limits but only catecholamines in serum and urine were remarkably higher. With a result of other detailed examinations, he was diagnosed as pheochromocytoma. He was referred to our clinic. Laparotomy was carried out under the strict monitoring of the circulation. We diagnosed his clinical status to non-hypertensive type. The tumor was 2.5 x 1.7 x 1.7 cm in size and weighed 10 g. After operation, serum and urine catecholamines returned to all within normal limits. a operation for the dermatoptosis was performed afterwards at the Department of Dermatology.
报告了1例与冯雷克林霍增氏病相关的嗜铬细胞瘤病例。一名53岁男性因胸部和腹部皮肤下垂到我院皮肤科就诊。他要求切除肿块。血液生化检查结果几乎在正常范围内,但血清和尿液中的儿茶酚胺明显升高。经过其他详细检查,他被诊断为嗜铬细胞瘤。他被转诊到我们科室。在严格的循环监测下进行了剖腹手术。我们将他的临床状态诊断为非高血压型。肿瘤大小为2.5×1.7×1.7厘米,重10克。术后血清和尿液中的儿茶酚胺均恢复到正常范围内。之后在皮肤科进行了皮肤下垂矫正手术。