A rare case of watery diarrhea, hypokalemia and achlorhydria syndrome caused by pheochromocytoma

[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.