S. Cannavo et al., COEXISTENCE OF GROWTH HORMONE-SECRETING PITUITARY-ADENOMA AND INTRACRANIAL MENINGIOMA - A CASE-REPORT AND REVIEW OF THE LITERATURE, Journal of endocrinological investigation, 16(9), 1993, pp. 703-708
The simultaneous occurrence of a pituitary adenoma and an intracranial
meningioma is a rare event. We report the coexistence of an eosinophi
lic pituitary adenoma and a endotheliomatous meningioma, in the sellar
region, and evaluate their endocrine, neuro-radiological and immunohi
stochemical pattern. A 47-year-old woman affected by acromegaly was re
ferred to us. Serum GH level was 82 ng/ml and remained unresponsive to
both OGTT (75 g per os) and iv. GHRH 1-29 (100 ug); IGF-1 was 807 ng/
ml. Eight hours after acute sc administration of octreotide (100 ug) G
H returned to normal levels (2.3 ng/ml). CT scan showed a large intra-
and suprasellar mass involving the right cavernous sinus, with a retr
osellar extension along the tentorium. A slight and inhomogeneous enha
ncement, with a periferal rim of bright signal was apparent at MRI. Co
nversely, the retrosellar component showed a bright homogeneous enhanc
ement. The patient, therefore, underwent neurosurgery. Histological ex
amination revealed the coexistence of 2 types of tissue: areas of endo
theliomatous meningioma were interspersed among sheets of acidophilic
adenoma tissue. Immunohistochemical analysis was performed in order to
determine the relationship between the two masses: a positive stainin
g for GH was shown in the areas of adenoma, as against for GHRH, neith
er in the adenomatous tissue nor in the slices of meningioma. Although
MRI showed a latero-sellar post-surgical residual of meningioma, seru
m GH value was <1 ng/ml. In conclusion, the relationship beetwen the G
H-secreting adenoma and the meningioma is unclear; however the GH-hype
rsecretion is not induced by a hypothetic GHRH-activity from the menin
gioma.