Abstract
The coexistence of pheochromocytoma and primary adrenal Cushing’s syndrome of the same adrenal gland has rarely been reported. We describe here the case of a female patient presenting with mild Cushing’s stigmata, hypertension and diabetes mellitus in whom we diagnosed a pheochromocytoma of the left adrenal gland with coexisting non-ACTH-dependent cortisol hypersecretion. While hormonal work-up was still in progress, the patient became pregnant and wanted to carry her pregnancy to full-term. A laparoscopic adrenalectomy in the 17th week of gestation was decided upon and the patient accordingly prepared for surgery by pre-treatment with phenoxybenzamine. Successful surgery — the first ever reported laparoscopic resection of a pheochromocy-toma in pregnancy — without perioperative complications was performed under general anesthesia, with the patient receiving peri- and post-operative hydrocortisone substitution. Pathohistological examination revealed a pheochromocytoma with positive immunostaining for interleukin-6 (IL-6) and negative immunostaining for ACTH, vasoactive intestinal polypeptide (VIP) and cytochrome P450, and with no signs of malignancy. A paracrine stimulation of the ipsilateral adrenal cortex by IL-6 produced by the pheochromocytoma, leading to cortical hyperplasia and subclinical Cushing’s syndrome, is suggested by the positive immunostaining for IL-6 and the MRI findings. Post-operatively, secondary adrenal insufficiency ensued, necessitating continuing hydrocortisone replacement over 12 months. Hypertension resolved after surgery, and diabetes after the uncomplicated vaginal delivery at term.
Similar content being viewed by others
References
Reincke M., Nieke J., Krestin G.P., Saeger W., Allolio B., Winkelmann W. Preclinical Cushing’s syndrome in adrenal inciden-talomas — comparison with adrenal Cushing’s syndrome. J. Clin. Endocrinol. Metab. 1992, 75: 826–832.
Terzolo M., Osella G., Ali A., Borretta G., Cesario F., Paccotti P., Angeli A. Subclinical Cushing’s syndrome in adrenal inciden-taloma. Clin. Endocrinol. (Oxf.) 1998, 48: 89–97.
Bravo E.L. Evolving concepts in the pathophysiology, diagnosis, and treatment of pheochromocytoma. Endocr. Rev. 1994, 15: 356–368.
Heaney A.P., Harper R., Ennis C., Rooney D.P., Sheridan B., Atkinson A.B., Bell P.M. Insulin action and hepatic glucose cycling in Cushing’s syndrome. Clin. Endocrinol. (Oxf.) 1997, 46: 735–743.
Wajchenberg B.L., Mendonca B.B., Liberman B., Pereira M.A.A., Carneiro P.C., Wakamatsu A., Kirschner M.A. Ectopic adrenocorticotropic hormone syndrome. Endocr. Rev. 1994, 15: 752–787.
Obrien T., Young W.F., Davila D.G., Scheithauer B.W., Kovacs K., Horvath E., Vale W., Vanheerden J.A. Case of the month — Cushing’s syndrome associated with ectopic production of corticotrophin-releasing hormone, corticotrophin and vasopressin by a phae-ochromocytoma. Clin. Endocrinol. (Oxf.) 1992, 37: 460–467.
Sonino N., Boscaro M., Paoletta A., Mantero F., Ziliotto D. Ketoconazole treatment in Cushing’s syndrome — experience in 34 patients. Clin. Endocrinol. (Oxf.) 1991, 35: 347–352.
Miller J.W., Crapo L. The medical treatment of Cushing’s syndrome. Endocr. Rev. 1993, 14: 443–458.
Schenker J.G., Granat M. Phaeochromocytoma and pregnancy: an updated appraisal. Aust. N. Z. J. Obstet. Gynaecol. 1982, 22: 1–10.
Burgess III G.E. Alpha blockade and surgical intervention of pheochromocytoma in pregnancy. Obstet. Gynecol. 1979, 53: 266–270.
Oishi S., Sato T. Pheochromocytoma in pregnancy: a review of the Japanese literature. Endocr. J. 1994, 41: 219–225.
Gordon R.D., Bachmann A.W., Klemm S.A., Tunny T.J., Stowasser M., Storie W.J., Rutherford J.C. An association of primary aldosteronism and adrenaline-secreting phaeochromocytoma. Clin. Exp. Pharmacol. Physiol. 1994, 21: 219–222.
Tan G.H., Carney J.A., Grant C.S., Young W.F. Coexistence of bilateral adrenal phaeochromocy-toma and idiopathic hyperaldosteronism. Clin. Endocrinol. (Oxf.) 1996, 44: 603–609.
Nguyen H.L.T., Luong K.V.Q. Coexistence of primary aldosteronism and pheochro-mocytoma in a Vietnamese patient. Endocrinologist 1996, 6: 490–493.
Aiba M., Hirayama A., Ito Y., Fujimoto Y., Nakagami Y., Demura H., Shizume K. A compound adrenal medullary tumor (pheochro-mocytoma and ganglioneuroma) and a cortical adenoma in the ipsilateral adrenal gland. A case report with enzyme histochemical and immunohistochemi-cal studies. Am. J. Surg. Pathol. 1988, 12: 559–566.
Mathison D.A., Waterhose C.A. Cushing’s syndrome with hypertensive crisis and mixed adrenal cortical adenoma-pheochromocytoma (corticomedullary adenoma). Am. J. Med. 1969, 47: 635–641.
Michal M., Havlicek F. Corticomedullary tumors of the adrenal glands. Report of two cases. Association of corticomedullary tumor with spindle cell sarcoma. Pathol. Res. Pract. 1996, 192: 1082–1089.
Kitahara M., Mori T., Seki H., Washizawa K., Amano Y., Nakahata T., Takeuchi S., Inaba H., Hotchi M., Komiyama A. Malignant paraganglioma presenting as Cushing’s syndrome with virilism in childhood — production of cortisol, androgens, and adrenocorticotrophic hormone by the tumor. Cancer 1993, 72: 3340–3345.
Schwarz S. Fluorometric determination of urinary norepinephrine and epinephrine: assessment of the aluminiumoxide-trihydroxyindole method by the analysis of fluorescence spectra. Wien. Klin. Wochenschr. 1977, 89: 667–674.
Harper M.A., Murnaghan G.A., Kennedy L., Hadden D.R., Atkinson A.B. Phaeochromocytoma in pregnancy. Five cases and a review of the literature. Br. J. Obstet. Gynaecol. 1989, 96: 594–606.
Janetschek G., Finkenstedt G., Gasser R., Waibel U.G., Peschel R., Bartsch G., Neumann H.P.H. Laparoscopic surgery for pheochromocytoma: adrena-lectomy, partial resection, excision of paragangliomas. J. Urol. 1998, 160: 330–334.
Janetschek G., Altarac S., Finkenstedt G., Gasser R., Bartsch G. Technique and results of laparoscopic adrenalectomy. Eur. Urol. 1996, 30: 475–479.
Morio H., Terano T., Yamamoto K., Tomizuka T., Oeda T., Saito Y., Tamura Y., Sasano H. Serum levels of dehydroepiandrosterone sulfate in patients with asymptomatic cortisol producing adrenal adenoma: Comparison with adrenal Cushing’s syndrome and non-functional adrenal tumor. Endocr. J. 1996, 43: 387–396.
Wallace C., Toth E.L., Lewanczuk R.Z., Siminoski K. Pregnancy-induced Cushing’s syndrome in multiple pregnancies. J. Clin. Endocrinol. Metab. 1996, 81: 15–21.
Clayman R.V. Editorial Comment. J. Urol. 1998, 160: 334.
Lacroix A., Tremblay J., Rousseau G., Bouvier M., Hamet P. Brief report: Propranolol therapy for ectopic beta-adrenergic receptors in adrenal Cushing’s syndrome. N. Engl. J. Med. 1997, 337: 1429–1234.
Päth G., Bornstein S.R., Ehrhart-Bornstein M., Scherbaum W.A. Interleukin-6 and the interleukin-6 receptor in the human adrenal gland: Expression and effects on steroidogenesis. J. Clin. Endocrinol. Metab. 1997, 82: 2343–2349.
Takagi M., Egawa T., Motomura T., Sakumamochizuki J., Nishimoto N., Kasayama S., Hayashi S., Koga M., Yoshizaki K., Yoshioka T., Okuyama A., Kishimoto T. Interleukin-6 secreting phaeochromocytoma associated with clinical markers of inflammation. Clin. Endocrinol. (Oxf.) 1997, 46: 507–509.
Schmid K.W., Dockhorn Dworniczak B., Fahrenkamp A., Kirchmair R., Totsch M., Fischer Colbrie R., Bocker W., Winkler H. Chromogranin A, secretogranin II and vasoactive intestinal peptide in phaeochromocytomas and ganglioneuromas. Histopathology 1993, 22: 527–533.
Mazzocchi G., Malendowicz L.K., Nussdorfer G.G. Stimulatory effect of vasoactive intestinal peptide (VIP) on the secretory activity of dispersed rat adreno-cortical cells. Evidence for the interaction of VIP with ACTH receptors. J. Steroid Biochem. Mol. Biol. 1994, 48: 507–509.
Close C.F., Mann M.C., Watts J.F., Taylor K.G. ACTH-independent Cushing’s syndrome in pregnancy with spontaneous resolution after delivery: control of hypercortisolism with metyrapone. Clin. Endocrinol. (Oxf.) 1993, 39: 375–379.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Finkenstedt, G., Gasser, R.W., Höfle, G. et al. Pheochromocytoma and sub-clinical Cushing’s syndrome during pregnancy: Diagnosis, medical pre-treatment and cure by laparoscopic unilateral adrenalectomy. J Endocrinol Invest 22, 551–557 (1999). https://doi.org/10.1007/BF03343608
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/BF03343608