Retinal abnormalities, unrelated to visual pathway compression, in acromega
lic patients were originally described by Smail in 1972 (Smail JM. Primary
pigmentary degeneration of the retina and acromegaly in a case of pituitary
adenoma. Br J Ophthalmol 1972; 56: 25-31). He illustrated a case of primar
y pigmentary degeneration of the retina occurring in a patient with a chrom
ophobe adenoma of the pituitary gland. To the best of our knowledge this re
mains the sole, published case of this association. We report on two male p
atients, with an acromegalic appearance, one caused by a pituitary adenoma,
the other associated with a Rathke's cleft cyst, presenting to our departm
ent of ophthalmology with the clinical picture of pigmentary degeneration o
f the retina.