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Pregnancy in hyperprolactinaemic infertile women treated with vaginal bromocryptine: Report of two cases and review of the literature
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Ernesto de Mendis, Domenico B, Elisabetta M. Uneventful pregnancy in a patient treated with slow release lanreotide: a case report. J Clin Endocrinol Metab 1999; 84:1489-1492.
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Expression of somatostatin receptor SST4 in human placenta and the absence of octreotide effect on human placental growth hormone concentration during pregnancy
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Caron P, Buscail L, Beckers A, et al. Expression of somatostatin receptor SST4 in human placenta and the absence of octreotide effect on human placental growth hormone concentration during pregnancy. J Clin Endocrinol Metab 1997; 82:3771-3776.
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Caron, P.1
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Fassnacht M, Capeller B, Arlt W, et al. Octreotide LAR treatment throughout pregnancy in an acromegalic woman. Clin Endocrinol (Oxford) 2001; 55:411-415. The authors report the use of octreotide and lanreotide for the control of growth hormone excess throughout pregnancy, and report no adverse effects on the fetus. The neonate was also followed for 3 months. The study suggests that in selected patients, octreotide may be used in pregnancy to optimize the outcome, without compromising safety.
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Rapid enlargement and recurrence of a pre-existing intrasellar craniopharyngioma during the course of two pregnancies. Case report
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Diabetes insipidus after pituitary surgery: Incidence after traditional versus endoscopic transphenoidal approaches
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Shah S, Har-El G. Diabetes insipidus after pituitary surgery: incidence after traditional versus endoscopic transphenoidal approaches. Am J Rhinol 2001; 15:377-379. A good study involving 81 patients to assess short-term and long-term postoperative diabetes insipidus in patients who underwent traditional transphenoidal surgery and those who underwent a transnasal endoscopic procedure. There was a decrease in the incidence of diabetes insipidus in the immediate postoperative period in the endoscopic group. However, there was no difference on long-term follow-up.
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Am J Rhinol
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Shah, S.1
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Schulz S, Redlich A, Koppe I, et al. Carney complex: an unexpected finding during the puerperium. Gynecol Obstet Invest 2001; 51:211-213.
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19
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Reschke, K.1
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ACTH-dependent Cushing's syndrome in pregnancy with spontaneous resolution after delivery: Control of the hypercorticolism with metyrapone
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Close CF, Mann MC, Watts JF, Taylor KG. ACTH-dependent Cushing's syndrome in pregnancy with spontaneous resolution after delivery: control of the hypercorticolism with metyrapone. Clin Endocrinol (Oxford) 1993; 39:375-379.
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Close, C.F.1
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0035123832
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Recurrent ACTH-dependent Cushing's syndrome in multiple pregnancies and its treatment with metyrapone
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Hana V, Dokoupilova M, Marek J, Plavka R. Recurrent ACTH-dependent Cushing's syndrome in multiple pregnancies and its treatment with metyrapone. Clin Endocrinol (Oxford) 2001; 54:277-281.
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Hana, V.1
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0033005616
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Cushing's syndrome in pregnancy treated by ketoconozole: Case report and review of the literature
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Berwaerts J, Verhelst J, Mahler C, Abs R. Cushing's syndrome in pregnancy treated by ketoconozole: case report and review of the literature. Gynecol Endocrinol 1999; 13:175-182.
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Berwaerts, J.1
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Cushing's syndrome secondary to adrenal adenoma during pregnancy
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Lo CY, Lo CM, Lam KY. Cushing's syndrome secondary to adrenal adenoma during pregnancy. Surg Endosc 2002; 16:219-220. The authors describe two different ways of managing Cushing's syndrome by laparoscopic adrenalectomy both during and after pregnancy.
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Lo, C.Y.1
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Lam, K.Y.3
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24
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0035047054
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Maternal undernutrition during late gestation induces fetal over-exposure to glucocorticoids and intrauterine growth restriction (IUGR) and disturbances in the hypothalamo-pituitary-adrenal axis in the new born rat
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Lesage J, Blondeau B, Grino M, et al. Maternal undernutrition during late gestation induces fetal over-exposure to glucocorticoids and intrauterine growth restriction (IUGR) and disturbances in the hypothalamo-pituitary-adrenal axis in the new born rat. Endocrinology 2001; 142:1692-1702.
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0035025505
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Bilateral phaeochromocytoma in pregnancy heralding MEN syndrome IIA: A case report
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Tewaris KS, Steiger RM, Lam LM, et al. Bilateral phaeochromocytoma in pregnancy heralding MEN syndrome IIA: a case report. J Reprod Med 2001; 46:385-388. This is the first case of multiple endocrine neoplasia type IIA reported in pregnancy. A high degree of clinical suspicion in view of the bilateral phaeochromocytomas helped clinch the diagnosis. This early and accurate diagnosis during pregnancy enabled subsequent prophylactic thyroidectomy before the development of medullary carcinoma.
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J Reprod Med
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Tewaris, K.S.1
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Lam, L.M.3
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26
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0032861917
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Phaeochromocytoma and subclinical Cushing's syndrome during pregnancy: Diagnosis, medical pre-treatment and cure by laparoscopic unilateral adrenalectomy
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Finkenstedt G, Gasser RW, Hofle G, et al. Phaeochromocytoma and subclinical Cushing's syndrome during pregnancy: diagnosis, medical pre-treatment and cure by laparoscopic unilateral adrenalectomy. J Endocrinol Invest 1999; 22:555-557.
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Minimally invasive adrenalectomy for phaeochromocytoma during pregnancy
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Pace DE, Chiasson PM, Schlach CM, et al. Minimally invasive adrenalectomy for phaeochromocytoma during pregnancy. Surg Laparosc Endosc Percutan Tech 2002; 12:122-125. This is the second reported case of laparoscopic adrenalectomy for phaeochromocytoma, which was carried out at the beginning of the second trimester with a good obstetric outcome. This report re-enforces the role of minimal access surgery during pregnancy in the treatment of adrenal tumours.
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Surg Laparosc Endosc Percutan Tech
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Pace, D.E.1
Chiasson, P.M.2
Schlach, C.M.3
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