Angiographic abnormal vascularity in pituitary chromophobe adenoma is rare and only about ten cases have been presented in the literature so far. We have reported in this article a case of pituitary chromophobe adenoma with tumor stain demonstrated by carotid angiography.
The patient, 65-years-old farmer, was admitted to our clinic with complaints of visual dis-turbance which developed 25 years ago in the right and 10 years ago in the left. He also has suffered from generalized tonic-clonic convulsive seizure attack occurring once or twice a year since 1066, six years prior to his admission.
Neuroradiological examinations have revealed the presence of a large tumor in the supra-and parasellar region. A homogeneous tumor stain beginning in the capillary phase and lasting throughout the venous phase was demonstrated by bilateral carotid angiography. An enlarged tortuous inferior hypophyseal artery arising from the extradural portion of the left carotid siphon was running upward and posteriorly and seemed to feed the posterior portion of the tumor.
A fronto-temporal craniotomy was performed. The hypertrophied capsule of the tumor was excised and little tumor tissue was removed because the tumor cavity was almost empty and only blood was evacuated inside the tumor as if it were cavernous hemangioma or embolised aneurysm. The total dosage of 4, 000 rads of
60CO was irradiated postoperatively and the patient's visual dis-turbance was slightly improved.
The abnormal vascularity of pituitary chromophobe adenoma appears as two distinct systems. Hypertrophied branches arising from the extradural portion of the carotid artery which are seen early in the arterial phase were supposed to be capsular rather than parenchymal. The homo-geneous tumor blush which begins to appear in the capillary phase and lasts throughout the venous phase probably represents diffuse small vessels filling in the parenchyma.
These tumors have characteristic clinical features as followings;rapid tumor growth with rapid progression of clinical symptoms, the very large size of the tumor with bone invasion, an intimate relation to vital centers and tendency toward necrosis and spontaneous hemorrhage. In consider-ation of these features, these tumors may be designated as clinically malignant although the histological criteria of malignancy in chromophobe adenoma have not been clearly defined and are still subject to controversy.
The role and effectiveness of radiotherapy to these tumors are generally unknown and uncertain. We, however, have impression that the adequate radiotherapy is the last measures to treat these tumors as it is difficult to be successfully removed by surgery.
View full abstract