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   <subfield code="a">Resistance to a long-acting somatostatin analog (SMS 201-995) reversed by surgery in acromegaly</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Roberto Attanasio, P. Chiodini, A. Liuzzi, P. Orlandi, C. De Palo, D. Dallabonzana, A. Lodrini, R. Cozzi]</subfield>
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   <subfield code="a">A 42-year-old woman had acromegaly and a large macroadenoma with supra- and parasellar extension. Her GH levels (median 85 ng/ml, range 63-170 ng/ml) were not responsive to TRH (200 μg iv), GHRH (100 μg iv) and bromocriptine (Br 2.5 mg po) acute tests; Sm-C level was 8 U/ml. She was treated with octreotide (SMS) (up to 1500 μg daily) for 3 months. No changes of clinical, biochemical and radiological findings were seen, therefore she underwent transsphenoidal surgery. After surgery, hypopituitarism and diabetes insipidus appeared: GH levels remained high (median 45 ng/ml; range 37-56 ng/ml), but became responsive to Br acute test. The patient was given SMS again, and this resulted in clinical improvement, marked reduction of GH and Sm-C levels and slight shrinkage of the residual tumor. Speculative hypotheses about this previously unreported phenomenon might be either an excess of both GHRH and somatostatin, caused by a primary increase of dopaminergic tone, or a primary excess only of GHRH; in both cases the surgical lesion of the hypothalamic-pituitary region might have impaired the neurohormones inflow to the residual pituitary and so let SMS and Br exert their inhibitory actions on GH secretion.</subfield>
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   <subfield code="a">Italian Society of Endocrinology (SIE), 1990</subfield>
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