Baba T, Machida K, Ozaki I, Okushima T, Murabayashi S, Kamata Y, Imamura K, Takebe K
Endocrinol Jpn. 1985 Apr;32(2):337-45. doi: 10.1507/endocrj1954.32.337.
A case of malignant pheochromocytoma, with a recurrence 17 years after the initial diagnosis of benign pheochromocytoma, was presented. The autopsy revealed multiple metastases of pheochromocytoma to the bone marrow of the thoracic and lumbar vertebrae. Of particular note is the fact that the patient was associated with paralytic ileus, polyuria and hypercalcemia and that he died of hypercalcemia crisis. Cases like this appear to be very rare.
报告了一例恶性嗜铬细胞瘤病例，该病例在最初被诊断为良性嗜铬细胞瘤17年后复发。尸检显示嗜铬细胞瘤多处转移至胸椎和腰椎骨髓。特别值得注意的是，该患者伴有麻痹性肠梗阻、多尿和高钙血症，最终死于高钙血症危象。这样的病例似乎非常罕见。
