13 March 2023: Articles
Successful Surgical Management of Gastric Antral Vascular Ectasia in a Patient with End-Stage Renal Disease: A Case Report and Literature Review
Unknown etiology, Management of emergency care, Rare disease, Educational Purpose (only if useful for a systematic review or synthesis), Rare coexistence of disease or pathologyBader H. Alsaeed1BDE, Ayesha A. AlAbdulqader1BDE, Ali A. Al-Qadhi 1BEF, Hawra A. Alaswad1BE, Mohammed S. Foula1ADEF*, Saeed J. Alshomimi1AE
Am J Case Rep 2023; 24:e938543
BACKGROUND: Gastric antral vascular ectasia (GAVE) is a rare clinical entity that presents with acute upper-gastrointestinal bleeding or chronic anemia. It is characterized by endoscopic watermelon appearance of the stomach. It is usually associated with other comorbidities; however, few articles have previously described GAVE in patients with end-stage renal disease. Its management is controversial, and endoscopic management is considered the treatment of choice.
CASE REPORT: A middle-age female patient, on regular hemodialysis for ESRD, was referred to the surgical out-patient clinic as a refractory GAVE after failure of endoscopic management as she became blood transfusion-dependent. She underwent laparoscopic subtotal gastrectomy with a Billroth II reconstruction of gastrojejunostomy. She had a smooth postoperative course and was followed up in the clinic for 12 months with no complications. Her hemoglobin level was stable at 9.4 g/dL without further blood transfusion.
CONCLUSIONS: Gastric antral vascular ectasia is usually associated with other comorbidities; however, an association between GAVE and CKD is rare. Its management is controversial, and endoscopic management is considered the preferred method of treatment. Laparoscopic subtotal gastrectomy is an effective management modality for GAVE, with dramatic improvement and good outcomes in terms of bleeding, blood transfusion requirements, and nutritional status.
Keywords: Blood Transfusion, Gastric Antral Vascular Ectasia, Gastric Bypass, Gastrointestinal Hemorrhage, Renal Insufficiency, Chronic
Gastric antral vascular ectasia (GAVE) is a rare clinical entity accounting for 4% of non-variceal upper-gastrointestinal bleeding. It is characterized by endoscopic watermelon appearance of the stomach [1–3]. Typically, it is presented by upper-gastrointestinal bleeding leading to chronic anemia [4,5]. GAVE is usually associated with various comorbidities. However, few articles have previously described GAVE in patients with end-stage renal disease (ESRD).
Herein, we describe a successful surgical management of a middle-aged woman on regular hemodialysis for ESRD who became a blood transfusion-dependent and was found to have GAVE.
A 54-year-old female patient was referred to the upper-gastrointestinal surgery clinic as a case of GAVE refractory to endoscopic management. She was known to have ESRD, diabetes mellitus, and hypertension. She had been on hemodialysis for 6 years. A year prior to presentation, she became blood transfusion-dependent with a baseline hemoglobin level of 4.5–6.1 g/dL, receiving 1 unit of packed RBCs during each dialysis session.
She underwent esophagogastroduodenoscopy and colonos-copy, which revealed a typical watermelon appearance of the stomach, with prominent erythematous folds in the antrum, features suggestive of GAVE (Figure 1). She was managed by endoscopic argon plasma coagulation (APC) that was repeated 3 times, with no noticeable clinical or endoscopic improvement.
Upon presentation to the surgical clinic, she was pale and undernourished, with bilateral lower-limb edema. Laboratory test results were significant for normocytic normochromic anemia and positive occult blood in the stool. Renal function tests were typical for ESRD. Other lab results, including liver function test and coagulation profile, were unremarkable.
After thorough counseling, she underwent a laparoscopic subtotal gastrectomy with a Billroth II reconstruction of gastrojejunostomy. Under general anesthesia, she was placed in a supine anti-Trendelenburg position. Diagnostic laparoscopy showed small amounts of ascites, with a huge fatty liver. The stomach was dissected from the mid-body downward to the pylorus using a sealing device, starting with the greater omentum followed by the lesser omentum. The stomach was transected 1 cm proximal to the pylorus and at the level of the mid-body. Gastrojejunostomy was then performed 60 cm distal to the duodeno-jejunal junction. The blood loss was minimal (around 50 milliliters). The total procedure duration was 115 minutes.
The patient had a smooth postoperative course. A water-soluble study on the third postoperative day excluded leakage. Gradually, she started oral intake and was eventually discharged home on the seventh postoperative day in good condition. She was followed up in the clinic for 1 year with no concerns and good nutritional status. Her hemoglobin level was stable at 9.4 g/dL without further blood transfusions. Her albumin level increased from 1.9 g/dL preoperatively to 3.7 g/dL 1 year postoperatively.
GAVE is a rare clinical entity with unknown etiology [2,3]. GAVE is usually associated with various systemic diseases, especially autoimmune diseases. Around 30% of patients with GAVE have liver cirrhosis . Other associated systemic diseases include Sjogren’s syndrome, systemic lupus syndrome, systemic sclerosis, Raynaud’s disease, DM, hypertension, acute myeloid leukemia, and bone marrow transplant [6–9]. Rarely, GAVE has been reported in patients with chronic kidney diseases. We performed a literature review using the terms “gastric antral vascular ectasia,” “GAVE,” “watermelon stomach,” “ESRD,” “chronic kidney disease,” “uremia,” and “hemodialysis” in databases of PubMed, Scopus, Medline, and Google scholar and identified 31 cases of GAVE in patients with chronic kidney diseases (Table 1).
GAVE is a disease of elderly people, with a female predominance in hepatic patients and male predominance in all other patients. This can be explained by the age and sex distribution of associated comorbidities .
Diagnosis of GAVE depends mainly on its characteristic endoscopic features: parallel red stripes of tortuous ectatic vessels, usually located at the antral mucosal folds . Moreover, it may extensively involve the whole stomach, giving a picture of honeycomb stomach, especially in cirrhotic patients [2,10]. However, the absence of the characteristic watermelon appearance does not entirely exclude the presence of GAVE, as the literature review shows that many patients required more than 1 endoscopy to confirm the presence of GAVE. Moreover, 7 cases (22.5%) in the literature review did not report this finding and were diagnosed based on clinical picture [12–16].
Management of GAVE is controversial, including various medical, endoscopic, and surgical management modalities. Several drugs have been tried in such patients, including estrogen and progesterone analogs, octreotide, and pulse steroids . The effectiveness of medical management is questionable, as only 16.1% of patients with GAVE and CKD in our literature review were successfully managed using only a medical approach.
Nowadays, endoscopic management is considered as the plan of choice. Several techniques have been used, including APC, laser, and sclerotherapy. APC is more easily tolerated, with fewer adverse effects, than other endoscopic techniques. Usually, multiple sessions of APC are required to control bleeding.
However, repeated sessions may lead to stenosis, gastric outlet obstruction, or perforation .
In general, surgical management for GAVE is considered as a last option after the failure of other management modalities . However, the clinical improvement of patients was much more noticeable after surgical management vs medical or endoscopic management, in the form of a stable hemoglobin level without blood transfusion. Multiple procedures have been reported as partial vs total gastrectomy and gastroesophagectomy [17,19]. In our literature review, only 2 patients (6.5%) underwent surgical management owing to extensive disease or after the failure of non-operative modalities [4,19].
Our patient was dependent on blood transfusion, with an average transfusion of 3 packed RBCs weekly. Initially, she was managed with 3 sessions of endoscopic APC, which failed to improve her anemia or reduce her transfusion requirements. The gastroenterologist referred her to us as a refractory case for endoscopic management. Therefore, surgical management was considered after multidisciplinary meetings owing to failure of the endoscopic management as well as fear of repeated blood transfusion complications. The patient underwent laparoscopic subtotal gastrectomy with Billroth II reconstruction. The laparoscopic approach has well-known advantages over the open approach. The histopathological examination was consistent with GAVE. During close follow-up visits, the patient had a stable hemoglobin level and did not require any blood transfusion.
Herein, we highlight the efficacy of surgical management in patients with GAVE. Indeed, the laparoscopic subtotal gastrectomy approach may be considered as an effective modality of management, along with endoscopic management, owing to its favorable outcomes, in terms of bleeding, blood transfusion requirements, and nutritional status, with low complication rates if performed in a well-equipped center by an expert laparoscopic surgeon. Further well-designed studies are required to assess the efficacy and outcome of the laparoscopic subtotal gastrectomy approach as first-line management for GAVE.
Gastric antral vascular ectasia is a rare clinical entity that presents with acute upper-gastrointestinal bleeding or chronic anemia. It is usually associated with other comorbidities; however, an association between GAVE and CKD is rare. Its management is controversial, and endoscopic management is considered the preferred method of treatment. Laparoscopic subtotal gastrectomy is an effective management modality for GAVE, with dramatic improvement and good outcomes in terms of bleeding, blood transfusion requirements, and nutritional status.
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