| Literature DB >> 28751427 |
Palittiya Sintusek1, Thanita Thammarakcharoen2, Shanop Shuangshoti3, Boosba Vivatvakin1.
Abstract
Chronic watery diarrhoea can be a presentation of gastrointestinal disease itself or a less-evident systemic disease. A 17-month-old boy presented with intractable diarrhoea, failure to gain weight, refractory tachycardia and severe hypertension. The ability to recognise and make a quick diagnosis of secretory type of diarrhoea dictated the outcome of patients with this ailment. Catecholamine hypersecretion was considered with the additional clues of refractory tachycardia and hypertension, a well-recognised phenomenon of neuroblastic tumours. A neuroblastic tumour can lead to vasoactive intestinal peptide (VIP) overexpression, which may result in secretory diarrhoea. In this situation, measurements of plasma VIP enabled crucial diagnosis. Imaging studies were used to identify and localise a neuroblastic tumour. Subsequent removal of the tumour was curative and led to the resolution of the symptoms. © BMJ Publishing Group Ltd (unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted.Entities:
Keywords: Gastroenterology; Gastrointestinal hormones; Neuroendocrinology; Neurogastroenterology
Mesh:
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Year: 2017 PMID: 28751427 PMCID: PMC5612006 DOI: 10.1136/bcr-2016-217532
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X