Testing, testing, testing: an insidious hypereosinophilia

Aim of the study: This case focuses on the difficulty in recognizing this rare entity characterized by systemic vasculitis in patients with history of asthma. Clinical case: We report a case of a 46-year-old man with history of allergic rhinitis and referred episodes of shortness of breath recognizi...

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Main Authors: Livia Robbiolo, Annalisa Carbone, Fabrizio Favales, Barbara Spelta, Fabrizio Colombo
Format: Article
Language:English
Published: PAGEPress Publications 2013-04-01
Series:Italian Journal of Medicine
Subjects:
Online Access:http://www.italjmed.org/index.php/ijm/article/view/272
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spelling doaj-b368dc66f5a34792b19ccb1c626b0e762020-11-25T03:48:42ZengPAGEPress PublicationsItalian Journal of Medicine1877-93441877-93522013-04-013316316510.4081/itjm.2009.163226Testing, testing, testing: an insidious hypereosinophiliaLivia RobbioloAnnalisa CarboneFabrizio FavalesBarbara SpeltaFabrizio ColomboAim of the study: This case focuses on the difficulty in recognizing this rare entity characterized by systemic vasculitis in patients with history of asthma. Clinical case: We report a case of a 46-year-old man with history of allergic rhinitis and referred episodes of shortness of breath recognizing as acute bronchitis who presented with fever, skin eruption, peripheral eosonophilia, muscle weakness, abdominal pain and progressively dyspnea. <br />Methods: Chest radiograph and computed tomography on admission showed consolidation in both lung fields and pericardial effusion. P-serum ANCA were positive. Neurological examination revealed mononeuritis multiplex. A skin biopsy was performed with presence of eosinophil granulocytes. The condition did not respond to antibiotics. He was supposed to have vasculitis and steroid treatment was started at a dose of 1 mg/kg; eosinophilia decreased but there was no clinical improvement. Abdominal pains were progressively more severe; emergency laparotomy revealed ileum infiammation, histopathological examination was consistent with Churg-Strauss syndrome.http://www.italjmed.org/index.php/ijm/article/view/272EosinophiliaAbdominal painVasculitis.
collection DOAJ
language English
format Article
sources DOAJ
author Livia Robbiolo
Annalisa Carbone
Fabrizio Favales
Barbara Spelta
Fabrizio Colombo
spellingShingle Livia Robbiolo
Annalisa Carbone
Fabrizio Favales
Barbara Spelta
Fabrizio Colombo
Testing, testing, testing: an insidious hypereosinophilia
Italian Journal of Medicine
Eosinophilia
Abdominal pain
Vasculitis.
author_facet Livia Robbiolo
Annalisa Carbone
Fabrizio Favales
Barbara Spelta
Fabrizio Colombo
author_sort Livia Robbiolo
title Testing, testing, testing: an insidious hypereosinophilia
title_short Testing, testing, testing: an insidious hypereosinophilia
title_full Testing, testing, testing: an insidious hypereosinophilia
title_fullStr Testing, testing, testing: an insidious hypereosinophilia
title_full_unstemmed Testing, testing, testing: an insidious hypereosinophilia
title_sort testing, testing, testing: an insidious hypereosinophilia
publisher PAGEPress Publications
series Italian Journal of Medicine
issn 1877-9344
1877-9352
publishDate 2013-04-01
description Aim of the study: This case focuses on the difficulty in recognizing this rare entity characterized by systemic vasculitis in patients with history of asthma. Clinical case: We report a case of a 46-year-old man with history of allergic rhinitis and referred episodes of shortness of breath recognizing as acute bronchitis who presented with fever, skin eruption, peripheral eosonophilia, muscle weakness, abdominal pain and progressively dyspnea. <br />Methods: Chest radiograph and computed tomography on admission showed consolidation in both lung fields and pericardial effusion. P-serum ANCA were positive. Neurological examination revealed mononeuritis multiplex. A skin biopsy was performed with presence of eosinophil granulocytes. The condition did not respond to antibiotics. He was supposed to have vasculitis and steroid treatment was started at a dose of 1 mg/kg; eosinophilia decreased but there was no clinical improvement. Abdominal pains were progressively more severe; emergency laparotomy revealed ileum infiammation, histopathological examination was consistent with Churg-Strauss syndrome.
topic Eosinophilia
Abdominal pain
Vasculitis.
url http://www.italjmed.org/index.php/ijm/article/view/272
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