Obscure gastrointestinal bleeding persisting for a decade: a rare manifestation of a common disease
Surinder S. Rana, Vishal Sharma, Chalapathi Rao, Kartar Singh, Deepak K. Bhasin
Post Graduate Institute of Medical Education and Research (PGIMER), Chandigarh, India
Department of Gastroenterology, Post Graduate Institute of Medical Education and Research (PGIMER), Chandigarh 160012, India
Conflict of Interest: None
Correspondence
to: Dr Surinder Singh Rana, Asst. Prof.,
Department of Gastroenterology, Postgraduate
Institute of Medical
Education and Research (PGIMER), Chandigarh, India 160012,
Tel: +91 172 2749123, Fax: +91 172 2744401,
e-mail: drsurinderrana@yahoo.co.in, sonalisurinder@yahoo.co.in
Received 16 February 2012; accepted 26 March 2012
Abstract
Celiac disease commonly presents with diarrhea but variable presentation with anemia, osteoporosis, incidental recognition, and liver function abnormalities is also known. Overt blood loss is uncommon in celiac disease. We present the case of a 60-year-old female who presented with obscure gastrointestinal blood loss for more than a decade necessitating multiple transfusions and was eventually diagnosed to have celiac disease. After introduction of gluten-free diet, her symptoms improved and there has been no recurrence of gastrointestinal bleeding.
Keywords celiac disease, capsule endoscopy, gastrointestinal bleeding
Introduction
Celiac disease is an autoimmune enteropathy precipitated by exposure to gluten. Although initially considered a rare malabsorption syndrome in children, it is now recognized as a systemic disorder with varying presentation and multiple manifestations affecting both pediatric and adult populations [1]. It commonly presents with diarrhea in children, whereas in adults the presentation is variable and may include anemia, osteoporosis, and liver function abnormalities [1,2]. Although occult gastrointestinal blood loss is common [3], overt bleeding is uncommon. We present the case of a 60-year-old lady who presented with obscure gastrointestinal blood loss for more than a decade necessitating multiple transfusions until celiac disease was eventually diagnosed.
Case report
A 60-year-old lady was referred to us for melena of 12 years duration. She had earlier undergone repeat evaluations at multiple private hospitals. She was initially diagnosed with duodenal ulcer and underwent exploratory laparotomy with pyloroplasty and truncal vagotomy. However, she rebled and thereafter underwent antrectomy with retrocolic gastrojejunostomy. She also received proton pump inhibitors, and eradication therapy for Helicobacter pylori. Despite the aggressive treatment, the patient continued to have melena episodes and required multiple blood transfusions (~170 transfusions over a decade). Her esophagogastroduodenoscopy, colonoscopy and barium meal follow through did not reveal any abnormality. Contrast enhanced computed tomography (CECT) of abdomen and the technetium-99m red blood cell scan were also non-contributory. A capsule endoscopy was performed by placing capsule in efferent limb under endoscopic guidance (Fig. 1). It revealed multiple ulcers of varying sizes throughout the small bowel (Fig. 2). As there was no history of non steroidal anti inflammatory drugs (NSAID) ingestion, a possibility of chronic non-specific small bowel ulcers was kept. Antinuclear antibodies and anti-neutrophil cytoplasmic antibodies were negative. However, IgA anti-tissue transglutaminase and anti-gliadin antibodies were positive. Antegrade double balloon enteroscopy was performed and biopsies were obtained from ulcer edge as well as mucosal folds. Histological examination of the biopsies from the ulcer edge revealed chronic inflammation and from the mucosal folds revealed increased intraepithelial lymphocytes. She was started on prednisolone 40 mg daily along with gluten-free diet. The melena subsided and thereafter steroids were tapered off. She remains well after one-year follow up, there has been no recurrence of bleeding and her hemoglobin has risen to 13.4 mg/dL.
Discussion
Celiac disease is an autoimmune disorder characterized by sensitivity to gluten. It can be complicated by occurrence of ulcerative jejunoileitis or malignant transformation [1]. Celiac disease has been associated with occult gastrointestinal blood loss [3,4]. In a study in children, occult gastrointestinal blood loss was reported in around one-fourth of patients and improved with gluten-free diet [3]. However, another study which utilized the more specific direct radiochromium-labeled red blood cells indicated that the blood loss was infrequent and the traditional colorimetric test were false positive probably due to excess intestinal cell loss or malabsorption affecting peroxidase containing foods [5]. Overt gastrointestinal blood loss in a patient with celiac disease may point to presence of malignancy like enteropathy-associated T cell lymphoma or adenocarcinoma, ulcerative jejunoileitis, vitamin K deficiency, occasionally due to varices, which may result from associated portal vein thrombosis or chronic liver disease, or other unrelated causes [6-9].
In our patient the capsule endoscopy revealed multiple ulcers in the small bowel. She was initially thought of having chronic non-specific ulceration of the small bowel. However, eventually celiac disease was found to be the cause of overt gastrointestinal bleeding in our patient. She improved after treatment with steroids and initiation of gluten-free diet and remained well with a rise in hemoglobin even after steroids were tapered. The long duration of the disease, the complete response after the introduction of gluten-free diet, and the absence of refractory symptoms suggest that these ulcers may have been benign. The etiology of these ulcers is not clear but,similar to the aphthous ulcers in the oral cavity of celiac disease patients, they might be immunologically mediated. Absence of relapse on gluten-free diet also suggests that the exclusion of the antigen from the diet may have led to remission.
The surgically altered proximal bowel also complicated the evaluation of the patient. Capsule endoscopy may be indicated in patients with celiac disease for evaluation of acute abdominal pain or occult gastrointestinal blood loss and is particularly useful in evaluation of complicated celiac disease [10,11]. In certain cases of iron deficiency anemia the diagnosis of celiac disease may be established only after capsule endoscopy [12]. The present report is also important as it highlights celiac disease with mucosal ulcerations as a cause of overt gastrointestinal blood loss. An earlier report had implicated celiac-related lymphocytic gastritis as a cause of fatal gastrointestinal blood loss even in the absence of malignant transformation [13]. Mucosal ulceration of the small intestine, especially jejunum, is common in celiac disease [14]. To conclude, celiac disease must be considered in the differential diagnosis in patients with obscure gastrointestinal bleeding and when ulcers are visualized in the small bowel.
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