White M C, Chahal P, Banks L, Joplin G F
Clin Endocrinol (Oxf). 1986 Jan;24(1):63-70. doi: 10.1111/j.1365-2265.1986.tb03255.x.
We report an 8-year follow-up of three sisters born of a consanguineous marriage and who originally presented with short stature and enlarged pituitary fossa. All have shown progressive failure of anterior pituitary hormone function. In addition, the two eldest sisters were eventually found to have an empty sella while the youngest, who initially showed an enhancing intrasellar mass consistent with a tumour, later showed an empty sella. A familial pituitary tumour developing early in childhood but subsequently undergoing involution could account for these findings.