Evidence map›Paper›PMID 41199358›Full record

ArticleJournal of medical case reports2025

A presentation of recurrent cerebral ischemic stroke in eosinophilic granulomatosis with polyangiitis: a case report.

Bryan Gregory, Ahmed Dawood Al Mahrizi, Harman Gill, Fatima Mossolem, Song Ang Peng, Randy Rueda, Eunseuk Lee

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In one paragraph

Article in Journal of medical case reports, 2025. 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Bryan GregoryRobert Wood Johnson Barnabas Health, 600 Kaplan Court, Toms River, NJ, 08753, USA. brydgregory@gmail.com.ORCID http://orcid.org/0009-0009-1198-669X
Ahmed Dawood Al MahriziFaculty of Medicine & Surgery, University of Malta, Msida, Malta.
Harman GillFutures Forward Research Institute, Toms River, NJ, USA.
Fatima MossolemFutures Forward Research Institute, Toms River, NJ, USA.
Song Ang PengRobert Wood Johnson Barnabas Health, 600 Kaplan Court, Toms River, NJ, 08753, USA.
Randy RuedaRobert Wood Johnson Barnabas Health, 600 Kaplan Court, Toms River, NJ, 08753, USA.
Eunseuk LeeRobert Wood Johnson Barnabas Health, 600 Kaplan Court, Toms River, NJ, 08753, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEosinophilic granulomatosis with polyangiitis is characterized as a small vessel vasculitis with the propensity to have a myriad of presentations due to the targeting of several different organ systems. More often than not, it is the pulmonary system that is affected. However, other reported presentations have included involvement of the skin, cardiovascular system, neurological system, renal, musculoskeletal, and even gastrointestinal tract in sequential order of increasing rarity. In most of these reported cases, only one or a couple of systems are involved. Here, the authors present a case of eosinophilic granulomatosis with polyangiitis that has peculiar and ominous involvement of both the neurological and gastrointestinal systems, lending to its extreme rarity as well as severity. CASE PRESENTATION: A 69-year-old Eastern European female patient was diagnosed with eosinophilic granulomatosis with polyangiitis exhibiting extensive multisystem involvement. Her case included a rare documented instance of hemorrhagic shock secondary to ileal gastrointestinal bleeding, occurring concurrently with multiple cerebral vascular infarctions.

conclusionThis case highlights the complexity and severity of eosinophilic granulomatosis with polyangiitis when it involves multiple organ systems simultaneously. It emphasizes the importance of recognizing eosinophilic granulomatosis with polyangiitis as a differential diagnosis in patients presenting with multisystem disease and unexplained eosinophilia. The report also underscores the need for aggressive management strategies and vigilance in diagnosing rare manifestations such as gastrointestinal hemorrhage and recurrent cerebral ischemic strokes.

Indexed as

Churg-Strauss SyndromeGastrointestinal HemorrhageGranulomatosis with PolyangiitisIschemic StrokeAgedDiagnosis, DifferentialFemaleHumansRecurrenceANCA positiveAutoimmune ischemic infarctChurg–StraussEosinophiliaEosinophilic granulomatosis with polyangiitisVasculitis

Identifiers

PMID41199358
PMCPMC12590678

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.