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https://doi.org/10.1186/s13256-016-0857-z
Title: | Amyloid light-chain amyloidosis presenting as abdominal bloating: A case report | Authors: | Lee, A.S.Y Lee, D.Z.Q Vasanwala, F.F |
Keywords: | amyloid protein congo red prokinetic agent alkylating agent antiinflammatory agent bortezomib cyclophosphamide dexamethasone adult amyloid light chain amyloidosis amyloidosis Article bloating bone marrow examination cardiomyopathy case report clinical feature differential diagnosis disease association dizziness follow up gastric amyloidosis gastroscopy human human tissue male medical history molecular dynamics motor neuropathy nerve conduction orthostatic hypotension priority journal protein determination protein function proteinosis retrospective study stomach biopsy stomach paresis weight reduction amyloidosis bone marrow complication Gastroparesis gastroscopy middle aged Paraproteinemias pathology treatment outcome Amyloidosis Anti-Inflammatory Agents Antineoplastic Agents, Alkylating Bone Marrow Bortezomib Cyclophosphamide Dexamethasone Gastroparesis Gastroscopy Humans Male Middle Aged Paraproteinemias Retrospective Studies Treatment Outcome |
Issue Date: | 2016 | Citation: | Lee, A.S.Y, Lee, D.Z.Q, Vasanwala, F.F (2016). Amyloid light-chain amyloidosis presenting as abdominal bloating: A case report. Journal of Medical Case Reports 10 (1) : 68. ScholarBank@NUS Repository. https://doi.org/10.1186/s13256-016-0857-z | Rights: | Attribution 4.0 International | Abstract: | Background: We present a case of amyloid light-chain amyloidosis with occult plasma cell dyscrasia, with the rare initial presentation of gastroparesis. While amyloidosis is known to affect the gastrointestinal system, rarely do patients present with gastrointestinal symptoms as their first symptom. To the best of our knowledge, this is the first such case reported with a definitive diagnosis made on gastroscopy. Case presentation: A 52-year-old Malay man with abdominal bloating, early satiety, and weight loss was found to have significant gastroparesis. He had a past medical history of stable non-ischemic cardiomyopathy. Results from initial screening were negative for common causes of gastroparesis, such as diabetes or offending medications. Gastroscopy did not show any mechanical gastric outlet obstruction. Our patient subsequently developed symptoms of postural giddiness, which then prompted further investigations for possible autonomic dysfunction. These finally revealed evidence of systemic involvement, including postural hypotension, speckled myocardium with infiltrative cardiomyopathy on a transthoracic echocardiogram, and multifocal motor neuropathy on nerve conduction studies, from which he had been relatively asymptomatic. These findings were collectively suggestive of infiltrative disease. Retrospective Congo red staining of a gastric biopsy specimen confirmed the diagnosis of gastric amyloidosis. The final diagnosis was amyloid light-chain amyloidosis secondary to plasma cell dyscrasia, which was confirmed by bone marrow examination. Our patients was started on chemotherapy and prokinetic agents, with some improvement in gastrointestinal symptoms on follow-up. Conclusion: We present this case to highlight that, although rare, gastroparesis can be the initial sole presentation of amyloidosis. It is important for the internist, gastroenterologist, and hematologist to consider amyloidosis as a differential diagnosis in the investigation of gastroparesis and to be vigilant in monitoring for other systemic involvement. © 2016 Lee et al. | Source Title: | Journal of Medical Case Reports | URI: | https://scholarbank.nus.edu.sg/handle/10635/179949 | ISSN: | 17521947 | DOI: | 10.1186/s13256-016-0857-z | Rights: | Attribution 4.0 International |
Appears in Collections: | Staff Publications Elements |
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