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challenging results on fdg pet/ct in a patient with uncontrolled celiac disease and small bowel adenocarcinoma
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نویسنده
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mohamedkhair ali ,al-ibraheem akram ,abdlkadir ahmed saad ,jaber omar
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منبع
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asia oceania journal of nuclear medicine and biology - 2022 - دوره : 10 - شماره : 2 - صفحه:155 -160
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چکیده
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Celiac disease (cd) is a chronic immune-mediated enteropathy that is caused by both environmental (gluten) and genetic (human leukocyte antigen (hla) and non-hla genes) factors. patients may be asymptomatic or exhibit atypical symptoms, necessitating a high index of suspicion for proper diagnosis. the evaluation of cd patients with 18f-fdg pet/ct imaging can be difficult, owing to the fact that this disease is inflammatory in nature. typical 18f-fdg pet/ct gastrointestinal manifestations of celiac disease include increased multifocal or diffuse bowel uptake, whereas single short segmental uptake is rarely encountered; thus, awareness of this wide range of findings is important to guide physicians through proper management and outcome. we report a case of small intestine adenocarcinoma and known cd complaining of recent episodes of diarrhea and weight loss that had a suspicious small bowel wall thickening that corresponds to a short segmental hypermetabolic process on fdg pet/ct follow-up scan. the patient was then referred to the gastroenterology department and underwent a colonoscopy, a biopsy was taken that revealed cd and was negative for malignancy. furthermore, 6 months later the abovementioned segmental fdg activity was completely resolved without any treatment received at the given time.
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کلیدواژه
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celiac disease ,single short segmental bowel uptake ,adenocarcinoma ,fdg pet/ct
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آدرس
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king hussein cancer center, department of nuclear medicine, jordan, king hussein cancer center, department of nuclear medicine, jordan. university of jordan, amman, school of medicine, jordan, king hussein cancer center, department of nuclear medicine, jordan, king hussein cancer center, department of pathology, jordan
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پست الکترونیکی
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oj.12785@khcc.jo
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Authors
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