Evidence map›Paper›PMID 40756741›Full record

ArticleCase reports in gastroenterology

Gastrointestinal Presentation of Eosinophilic Granulomatosis with Polyangiitis, Formerly Churg-Strauss Syndrome: A Case Report.

Muhammad Umair Tayyub, Arsh Gupta, Rabia Ashraf, Meenal Gupta, Priyan Tantrige, Howard Curtis, Vinod Audimoolam

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Article in Case reports in gastroenterology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Muhammad Umair TayyubDepartment of Gastroenterology, Kings College Hospital NHS Foundation Trust, London, UK.
Arsh GuptaDepartment of Pathology, Kings College Hospital NHS Foundation Trust, London, UK.
Rabia AshrafDepartment of Gastroenterology, Kings College Hospital NHS Foundation Trust, London, UK.
Meenal GuptaDepartment of Pathology, Kings College Hospital NHS Foundation Trust, London, UK.
Priyan TantrigeDepartment of Radiology, Kings College Hospital NHS Foundation Trust, London, UK.
Howard CurtisDepartment of Gastroenterology, Kings College Hospital NHS Foundation Trust, London, UK.
Vinod AudimoolamDepartment of Gastroenterology, Kings College Hospital NHS Foundation Trust, London, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Some of the most common presentations of gastrointestinal diseases are nausea, vomiting, and generalized abdominal pain. These symptoms could also be associated with other diseases and require a structured approach to the specific diagnosis. Eosinophilic granulomatosis with polyangiitis (EGPA), also known as Churg-Strauss syndrome, is a small and medium-sized vessel vasculitis that can affect any body system and present with a wide range of symptoms and atypical presentation. Therefore, diagnosis of this condition may not always be straightforward. Case Presentation: This case report presents a challenging case of a young man presenting with symptoms of abdominal pain, nausea, vomiting and non-specific symptoms of lethargy and fatigue. The case describes overlapping features with granulomatosis with polyangiitis (GPA) and anti-neutrophil cytoplasmic antibodies (ANCA)-positive and -negative vasculitis. The patient needed extensive workup and investigations to be eventually diagnosed with EGPA. In this case, myeloperoxidase (MPO) ANCA was negative, which is positive in the majority of EGPA cases, and this poses an additional diagnostic dilemma. Conclusion: The case highlights that non-specific complaints of vomiting and abdominal pain should be addressed methodically and not just be treated symptomatically.

Indexed as

Abdominal painAnti-neutrophil cytoplasmic antibodiesAnti-proteinase 3 antibodyEosinophilic granulomatosis with polyangiitisVomiting

Identifiers

PMID40756741
PMCPMC12316446

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