A rare case of watery diarrhea, hypokalemia and achlorhydria syndrome caused by pheochromocytoma
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Yingyong Hou | Xin Gao | Li Zhang | Zhaodi Wu | Zhiqiang Lu | Zhilong Ai | Jingjing Jiang
[1] V. Colantuoni,et al. Lessons to be learned from the clinical management of a MEN 2A patient bearing a novel 634/640/700 mutation of the RET proto‐oncogene , 2012, Clinical endocrinology.
[2] D. Metz,et al. Gastrointestinal neuroendocrine tumors: pancreatic endocrine tumors. , 2008, Gastroenterology.
[3] L. Buhl,et al. Adrenal Pheochromocytoma Producing Vasoactive Intestinal Peptide and Masking Hypertension , 2008, Hormone Research in Paediatrics.
[4] K. Kanagawa,et al. Hypokalemic rhabdomyolysis due to WDHA syndrome caused by VIP-producing composite pheochromocytoma: a case in neurofibromatosis type 1. , 2005, Japanese journal of clinical oncology.
[5] U. Lerner,et al. Expression and regulatory role of receptors for vasoactive intestinal peptide in bone cells , 2002, Microscopy research and technique.
[6] A. Vortmeyer,et al. The Journal of Clinical Endocrinology & Metabolism Printed in U.S.A. Copyright © 2001 by The Endocrine Society Pheochromocytomas in von Hippel-Lindau Syndrome and Multiple Endocrine Neoplasia Type 2 Display Distinct Biochemical and Clinical Phenotypes , 2022 .
[7] P. Lehenkari,et al. Vasoactive intestinal peptide regulates osteoclast activity via specific binding sites on both osteoclasts and osteoblasts. , 2000, Bone.
[8] I. Colin,et al. Acute Watery Diarrhea as the Initial Presenting Feature of a Pheochromocytoma in an 84-Year-Old Female Patient , 1999, Hormone Research in Paediatrics.
[9] M. Castro Cabezas,et al. A patient with neurofibromatosis type 1 and watery diarrhoea syndrome due to a VIP‐producing adrenal phaeochromocytoma , 1999, Journal of internal medicine.
[10] W. Linehan,et al. Plasma normetanephrine and metanephrine for detecting pheochromocytoma in von Hippel-Lindau disease and multiple endocrine neoplasia type 2. , 1999, The New England journal of medicine.
[11] G. Macphee,et al. A case of watery diarrhoea syndrome due to an adrenal phaeochromocytoma secreting vasoactive intestinal polypeptide with coincidental autoimmune thyroid disease. , 1987, Acta endocrinologica.
[12] S. Sackel,et al. Watery diarrhea syndrome due to an adrenal pheochromocytoma secreting vasoactive intestinal polypeptide , 1985, Digestive Diseases and Sciences.
[13] G. Viale,et al. Vasoactive intestinal polypeptide‐, somatostatin‐, and calcitonin‐producing adrenal pheochromocytoma associated with the watery diarrhea (WDHH) syndrome. First case report with immunohistochemical findings , 1985, Cancer.
[14] I. Khubchandani,et al. WDHA syndrome caused by pheochromocytoma: Report of a case , 1978, Diseases of the colon and rectum.
[15] R. Farmer,et al. Watery Diarrhea Syndrome: Two Unusual Cases and Further Evidence that VIP is a Humoral Mediator , 1978, Annals of surgery.
[16] P. Whorwell,et al. Watery diarrhoea and hypokalaemia associated with a phaeochromocytoma , 1975, Postgraduate medical journal.
[17] A. Morrison,et al. Islet cell tumor and a syndrome of refractory watery diarrhea and hypokalemia. , 1958, The American journal of medicine.
[18] T. P. Fox,et al. Pheochromocytoma producing vasoactive intestinal peptide. , 2002, Mayo Clinic proceedings.
[19] S. Pais. Angiographic demonstration of a vasoactive intestinal polypeptide-secreting pheochromocytoma in a patient with WDHA syndrome. , 1978, AJR. American journal of roentgenology.