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Case Report: Irreversible Watery Diarrhea, Severe Metabolic Acidosis, Hypokalemia and Achloridria Syndrome Related to Vasoactive Intestinal Peptide Secreting Malignant Pheochromocytoma.
- Source :
-
Frontiers in endocrinology [Front Endocrinol (Lausanne)] 2021 Mar 17; Vol. 12, pp. 652045. Date of Electronic Publication: 2021 Mar 17 (Print Publication: 2021). - Publication Year :
- 2021
-
Abstract
- Background: Pheochromocytoma (PHEO) clinical manifestations generally mirror excessive catecholamines secretion; rarely the clinical picture may reflect secretion of other hormones. Watery diarrhea, hypokalemia and achlorhydria (WDHA) is a rare syndrome related to excessive secretion of vasoactive intestinal peptide (VIP).<br />Clinical Case: A 73-year-old hypotensive man affected by adrenal PHEO presented with weight loss and watery diarrhea associated with hypokalemia, hyperchloremic metabolic acidosis (anion gap 15 mmol/l) and a negative urinary anion gap. Abdominal computed tomography scan showed a right adrenal PHEO, 8.1 cm in maximum diameter, with tracer uptake on <superscript>68</superscript> GaDOTA-octreotate positron emission tomography. Metastasis in lumbar region and lung were present. Both chromogranin A and VIP levels were high (more than10 times the normal value) with slightly elevated urine normetanephrine and metanephrine excretion. Right adrenalectomy was performed and a somatostatin analogue therapy with lanreotide started. Immunostaining showed chromogranin A and VIP co-expression, with weak somatostatin-receptor-2A positivity. In two months, patient clinical conditions deteriorated with severe WDHA and multiple liver and lung metastasis. Metabolic acidosis and hypokalemia worsened, leading to hemodynamic shock and exitus.<br />Conclusions: A rare case of WDHA syndrome caused by malignant VIP-secreting PHEO was diagnosed. High levels of circulating VIP were responsible of the rapidly evolving clinical picture with massive dehydration and weight loss along with severe hyperchloremic metabolic acidosis and hypokalemia due to the profuse untreatable diarrhea. The rescue treatment with lanreotide was unsuccessful because of the paucity of somatostatin-receptor-2A on VIP-secreting PHEO chromaffin cells.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2021 Negro, Verzicco, Tedeschi, Campanini, Zanelli, Negri, Farnetti, Nicoli, Palladini, Santi, Cunzi, Calvi, Coghi, Gerra, Volpi, Graiani and Cabassi.)
- Subjects :
- Acidosis complications
Adrenal Gland Neoplasms complications
Adrenal Gland Neoplasms diagnosis
Adrenalectomy
Aged
Chromaffin Cells cytology
Diarrhea complications
Humans
Hypokalemia complications
Male
Peptides, Cyclic therapeutic use
Peripheral Nervous System Neoplasms
Radionuclide Imaging
Receptors, Somatostatin therapeutic use
Somatostatin analogs & derivatives
Somatostatin therapeutic use
Syndrome
Tomography, X-Ray Computed
Weight Loss
Acidosis diagnosis
Diarrhea diagnosis
Hypokalemia diagnosis
Pheochromocytoma physiopathology
Vasoactive Intestinal Peptide chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1664-2392
- Volume :
- 12
- Database :
- MEDLINE
- Journal :
- Frontiers in endocrinology
- Publication Type :
- Academic Journal
- Accession number :
- 33815297
- Full Text :
- https://doi.org/10.3389/fendo.2021.652045