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DOI:
10.1097/01.ccm.0000551042.44049.2f
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发表时间:
2019-01
影响因子:
8.8
通讯作者:
N. Sawal;Ritu Modi;G. Johri
中科院分区:
文献类型:
--
作者:
N. Sawal;Ritu Modi;G. Johri
Methods: A 40-year old male presenting with encephalopathy and a two-year history of chronic diarrhea was admitted to the ICU for renal failure, severe hyponatremia (124), hypokalemia (1.7), hypophosphatemia (0.9) and normal anion gap metabolic acidosis (NAGMA) with pH of 6.8 on ABG. Despite aggressive electrolyte replacement and initiation on a bicarbonate drip he continued to have NAGMA and electrolyte abnormalities in the setting of persistent, watery diarrhea. Initial labs were significant for HIV with a CD4 count of 558, so infectious work-up was performed but was unremarkable. Due to reports of melena, sigmoidoscopy was done to evaluate for CMV colitis and revealed a 13mm submucosal rectal polyp identified as a well-differentiated carcinoid neuroendocrine tumor. Despite obtaining clean margins the patient continued to have diarrhea and EUS was done which suggested deeper tissue invasion however this was felt to be cautery artifact. Despite normal 5-HIAA levels, an octreotide scan was done and revealed no rectal uptake but localized to the left upper quadrant. CT abdomen revealed a left upper quandrant mesenteric mass arising from the pancreatic tail and EUS biopsy identified a VIPoma with metastatic spread. The patient was eventually started on octreotide and loperamide and noted significant improvement of his diarrhea and resolution of his electrolyte disorders.Results: VIPomas although rare, can cause severe and sometimes fatal dyselectrolytemias. This case highlights the importance of maintaining a clinical suspicion for underlying neuroendocrine malignancy even in immunocompromised hosts. In these cases, clinicians should have a low threshold for obtaining imaging or diagnostic testing to rule out non-infectious pathologies and avoid life-threatening complications.