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Going Round in Circles with a Multisystemic Disease: A Unique Case of Parasitic Aortitis

Aortitis results from aortic inflammation, frequent causes being infections and rheumatological disorders. The authors report the case of a 33-year-old black male with recent arterial hypertension, who presented with recurrent abdominal pain, jaundice, anorexia, weight loss and diarrhoea. Laboratory...

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Autores principales: Antunes, Maria Lobo, Cabral, Gonçalo, Tavares, Raquel, Noronha, Carla, Araújo, José
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SMC Media Srl 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6346790/
https://www.ncbi.nlm.nih.gov/pubmed/30755949
http://dx.doi.org/10.12890/2017_000601
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author Antunes, Maria Lobo
Cabral, Gonçalo
Tavares, Raquel
Noronha, Carla
Araújo, José
author_facet Antunes, Maria Lobo
Cabral, Gonçalo
Tavares, Raquel
Noronha, Carla
Araújo, José
author_sort Antunes, Maria Lobo
collection PubMed
description Aortitis results from aortic inflammation, frequent causes being infections and rheumatological disorders. The authors report the case of a 33-year-old black male with recent arterial hypertension, who presented with recurrent abdominal pain, jaundice, anorexia, weight loss and diarrhoea. Laboratory work-up was compatible with inflammatory anaemia and obstructive jaundice, while abdominal imaging revealed a dilated biliary tract, no visible gallstones, cephalic pancreatic globosity and aortic thickening. Pancreatic aspirate was negative for malignant cells, bacteria and Mycobacterium tuberculosis. The jaundice spontaneously subsided and the pancreatic globosity improved over time. Following positive PPD and IGRA, isoniazid was started. However, follow-up investigations revealed a severe bulbar stenosis with intense eosinophilic infiltrate, multiple non-necrotizing granulomas, and thoracic and abdominal aortitis not previously recognized. Immunological profile (ECA, ANCA and IgG4), eggs and parasites in stool samples were negative. The multisystemic disease, with an insidious and migrating behaviour, gastrointestinal and vascular involvement, granulomatous inflammatory response and tissue eosinophilia, raised the suspicion of a parasitic infestation (despite negative screening) or vasculitis. After 7 days of empirical treatment with albendazole and ivermectin, the patient passed a specimen of Ascaris lumbricoides in the stool and improved clinically. LEARNING POINTS: Parasitic infestations can cause aortitis: negative stool screening does not rule out roundworm infestation and granulomatous inflammatory response with eosinophilia is a histological hallmark. Infestation by Ascaris lumbricoides can have multisystemic expression and mimic rheumatological disorders such as vasculitis. This is the first report of a parasitic-related aortitis in humans.
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spelling pubmed-63467902019-02-12 Going Round in Circles with a Multisystemic Disease: A Unique Case of Parasitic Aortitis Antunes, Maria Lobo Cabral, Gonçalo Tavares, Raquel Noronha, Carla Araújo, José Eur J Case Rep Intern Med Articles Aortitis results from aortic inflammation, frequent causes being infections and rheumatological disorders. The authors report the case of a 33-year-old black male with recent arterial hypertension, who presented with recurrent abdominal pain, jaundice, anorexia, weight loss and diarrhoea. Laboratory work-up was compatible with inflammatory anaemia and obstructive jaundice, while abdominal imaging revealed a dilated biliary tract, no visible gallstones, cephalic pancreatic globosity and aortic thickening. Pancreatic aspirate was negative for malignant cells, bacteria and Mycobacterium tuberculosis. The jaundice spontaneously subsided and the pancreatic globosity improved over time. Following positive PPD and IGRA, isoniazid was started. However, follow-up investigations revealed a severe bulbar stenosis with intense eosinophilic infiltrate, multiple non-necrotizing granulomas, and thoracic and abdominal aortitis not previously recognized. Immunological profile (ECA, ANCA and IgG4), eggs and parasites in stool samples were negative. The multisystemic disease, with an insidious and migrating behaviour, gastrointestinal and vascular involvement, granulomatous inflammatory response and tissue eosinophilia, raised the suspicion of a parasitic infestation (despite negative screening) or vasculitis. After 7 days of empirical treatment with albendazole and ivermectin, the patient passed a specimen of Ascaris lumbricoides in the stool and improved clinically. LEARNING POINTS: Parasitic infestations can cause aortitis: negative stool screening does not rule out roundworm infestation and granulomatous inflammatory response with eosinophilia is a histological hallmark. Infestation by Ascaris lumbricoides can have multisystemic expression and mimic rheumatological disorders such as vasculitis. This is the first report of a parasitic-related aortitis in humans. SMC Media Srl 2017-05-17 /pmc/articles/PMC6346790/ /pubmed/30755949 http://dx.doi.org/10.12890/2017_000601 Text en © EFIM 2017 This article is licensed under a Commons Attribution Non-Commercial 4.0 License (https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Articles
Antunes, Maria Lobo
Cabral, Gonçalo
Tavares, Raquel
Noronha, Carla
Araújo, José
Going Round in Circles with a Multisystemic Disease: A Unique Case of Parasitic Aortitis
title Going Round in Circles with a Multisystemic Disease: A Unique Case of Parasitic Aortitis
title_full Going Round in Circles with a Multisystemic Disease: A Unique Case of Parasitic Aortitis
title_fullStr Going Round in Circles with a Multisystemic Disease: A Unique Case of Parasitic Aortitis
title_full_unstemmed Going Round in Circles with a Multisystemic Disease: A Unique Case of Parasitic Aortitis
title_short Going Round in Circles with a Multisystemic Disease: A Unique Case of Parasitic Aortitis
title_sort going round in circles with a multisystemic disease: a unique case of parasitic aortitis
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6346790/
https://www.ncbi.nlm.nih.gov/pubmed/30755949
http://dx.doi.org/10.12890/2017_000601
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