Cameron S, Allen I, Ozo C, Kennedy L, Atkinson B, Hadden D
Department of Pathology, Queen's University, Belfast, Northern Ireland, U.K.
J Pathol. 1990 Jul;161(3):239-44. doi: 10.1002/path.1711610311.
This paper reports the occurrence of a rare, yet distinct pituitary adenoma which was surgically removed from a 42-year-old male with both clinical and biochemical evidence of acromegaly and mild hyperprolactinaemia. The monomorphic adenoma consisted of mature cells which were ultrastructurally indistinguishable from those of a prolactinoma. Electron immunocytochemistry, including a series of double-labelling techniques using selected colloidal gold particles as markers, indicated the presence of a pituitary adenoma in which the cells were capable of simultaneously producing growth hormone and prolactin and packaging them within the same secretory granule. This is thought to represent a mammosomatotroph cell adenoma.