I. Quevedo et al., Pituitary apoplexy secondary to a metastatic renal cell carcinoma. Report of a case followed for seven years, REV MED CHI, 128(9), 2000, pp. 1015-1018
We report a man in whom a 15 cm. renal tumor was excised at the age of 49.
The pathological examination showed a clear cell carcinoma. Five years late
r, he presented with headache, vomiting and unilateral palpebral ptosis. Im
aging studies showed a sellar tumor with pituitary apoplexy. The tumor was
excised and the pathological study disclosed a clear cell tumor, positive f
or vimentin, cytokeratins AE1 and AE3 and immunohistochemically negative fo
r LH, TSH, ACTH and GH. Considering the similar histopathological features,
it was considered as a metastasis of the renal tumor. The patient was supp
lemented with thyroid, adrenal and gonadal hormones. Seven years later, he
presented a new tumor in the remaining kidney, that corresponded to a cysti
c papillary renal cell carcinoma. Afterwards, he presented a transitional u
rinary bladder tumor. Mortality associated to renal cell tumors is 90% at 5
years, and pituitary metastases are extraordinarily uncommon (Rev Med Chil
e 2000; 128: 1015-8).