A 73 years old female with known history of diffuse systemic scleroderma with pulmonary and renal involvement, presented with dizzy spells and 3 episodes of haematemesis over 1 week duration. On examination, she appeared to be pale with heart rate of 75/minute, blood pressure 163/71 mmHg and oxygen saturation 96% on room air. Abdominal examination revealed soft and nontender abdomen, normal bowel sounds with no organomegaly. Per rectal examination was unremarkable. Blood tests showed haemoglobin of 7.3 g/dl with MCV 88.8 fl. Iron profile showed total Iron 5.3 µmol/L, TIBC 54.1 µmol/L and Iron saturation of 10%. Liver function tests were with in the normal limits with AST 16 U/L, ALT 22U/L, ALP 59 U/L and total bilirubin 18 µmols/L. An ultrasound abdomen showed normal appearance of the liver, gall bladder, biliary tree, pancreas, aorta, and spleen. Hepatitis screen was –ve and vitamin B12, folic acid and thyroid functions were also with in the normal range.

She was transfused with three units of packed cells and an urgent upper gastrointestinal endoscopy was arranged. Endoscopy showed vascular lesions with erythematous linear streaks, consistent with Watermelon stomach. No active bleeding was noted. Biopsy report showed very mild chronic active gastritis with no evidence of intestinal type metaplasia, dysplasia or malignancy. Testing for H. Pylori was negative. She was prescribed proton pump inhibitors, oral iron supplements and was discharged home with close monitoring of full blood count.

Watermelon stomach or Gastric antral vascular ectasia (GAVE) is an uncommon but important cause of gastrointestinal blood loss and iron deficiency anaemia that is characterized by a distinctive endoscopic appearance consisting of parallel erythematous folds traversing the gastric antrum [1]. Most patients with GAVE suffer from liver cirrhosis, autoimmune disease, chronic renal failure and bone marrow transplantation [2]. A majority of patients without cirrhosis but with GAVE syndrome are female (71%) with median age of 73 years, whereas the majority of patients with both cirrhosis and GAVE syndrome are male (75%) with a mean age of 65 years [3]. Histological features include vascular ectasia within the mucosa, fibrin thrombi, fibrohyalinosis and spindle cell proliferation. However, biopsy specimens may miss the lesions because they are often focal; thus, the diagnosis is typically made based on the characteristic endoscopic appearance, making biopsy unnecessary [4]. Treatment can range from heater probe cautery, laser coagulation to surgical resection of the gastric antrum [5].