Erythropoietin resistance-secondary to watermelon stomach: a forgotten story in chronic kidney disease patients
Nikolaos Sabanis, Eleni Paschou
Corresponding author: Nikolaos Sabanis, Department of Nephrology, General Hospital of Trikala, Trikala, Greece
Received: 16 Aug 2022 - Accepted: 18 Jan 2023 - Published: 20 Jan 2023
Domain: Internal medicine,Nephrology
Keywords: Gastric antral vascular ectasia, watermelon stomach, erythropoietin resistance, chronic kidney disease
©Nikolaos Sabanis et al. Pan African Medical Journal (ISSN: 1937-8688). This is an Open Access article distributed under the terms of the Creative Commons Attribution International 4.0 License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Cite this article: Nikolaos Sabanis et al. Erythropoietin resistance-secondary to watermelon stomach: a forgotten story in chronic kidney disease patients. Pan African Medical Journal. 2023;44:40. [doi: 10.11604/pamj.2023.44.40.36839]
Available online at: https://www.panafrican-med-journal.com//content/article/44/40/full
Images in clinical medicine
Erythropoietin resistance-secondary to watermelon stomach: a forgotten story in chronic kidney disease patients
Erythropoietin resistance-secondary to watermelon stomach: a forgotten story in chronic kidney disease patients
&Corresponding author
Watermelon stomach, also known as gastric antral vascular ectasia (GAVE), is a rarely seen cause of acute upper gastrointestinal bleeding or chronic iron deficient anemia, revealed when gastroscopy is performed. GAVE affects predominantly women of advanced age and is usually associated with certain underlying co-morbidities including liver cirrhosis, autoimmune diseases and chronic kidney disease. Based on the above, we report the case of a 75-year-old woman under hemodialysis for six consecutive years due to end-stage renal disease attributable to hypertensive nephrosclerosis. The patient also suffered from chronic ischemic heart disease, severe peripheral artery disease and an unidentified connective tissue-disease characterized by high levels of anti-nuclear antibodies and clinical symptoms restrained in flares of non-erosive polyarthritis. Six months prior, she developed hyporesponsiveness to recombinant human erythropoietin (rEPO) due to iron deficiency despite the administration of the appropriate dose of intravenous iron as well as the exclusion of other co-existing causes of resistance, namely inadequate hemodialysis, inflammation, malnutrition, severe hyperparathyroidism and underlying hematologic disorders. Surprisingly, the patient experienced a sudden episode of severe upper gastrointestinal bleeding characterized by hemodynamic instability, hemoglobin fall and melena that required blood transfusions. Once hemodynamic stabilization was achieved, an upper endoscopic exam was performed showing the pathognomonic extensive vascular ectasias and patchy erythematosus lesions at the distal antrum. Thus, GAVE should be considered in the differential diagnosis of chronic kidney disease patients who present not only with acute blood loss but also with resistance to rEPO due to inadequate iron stores.
Figure 1: gastric antral vascular ectasia or watermelon stomach's endoscopic findings