Evidence map›Paper›PMID 40545682›Full record

ArticleThe American journal of case reports2025

Acute Acalculous Cholecystitis in a Child with COVID-19 and Influenza B: A Case Report.

Abdul Khaliq Abdul Jalil, Nafiza Mat Nasir, Nuryasmin Ramli, Zarina Yakof

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Article in The American journal of 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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5 · Who and what money

Authors and funding

4 authors.

Abdul Khaliq Abdul JalilDepartment of Primary Care Medicine, Faculty of Medicine, Universiti Teknologi MARA (UiTM), Sungai Buloh, Selangor, Malaysia.
Nafiza Mat NasirDepartment of Primary Care Medicine, Faculty of Medicine, Universiti Teknologi MARA (UiTM), Sungai Buloh, Selangor, Malaysia.ORCID 0000-0002-8022-5757
Nuryasmin RamliDepartment of Paediatrics, Hospital Sungai Buloh, Sungai Buloh, Selangor, Malaysia.
Zarina YakofDepartment of Radiology, Hospital Sungai Buloh, Sungai Buloh, Selangor, Malaysia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Acute acalculous cholecystitis (AAC) is a rare pediatric condition marked by gallbladder inflammation without gallstones. In children, symptoms are non-specific, making diagnosis and management challenging. Imaging, particularly ultrasound or computed tomography (CT) scan, often is the key to detection. Treatment typically involves supportive care and antibiotics, with surgery reserved for severe cases. This report describes the case of a 7-year-old Malaysian boy with a history of COVID-19 and influenza B infection presenting with acute acalculous cholecystitis. CASE REPORT A 7-year-old Malaysian boy presented with fever, vomiting, and abdominal pain, initially diagnosed as acute gastroenteritis at primary care clinic. As symptoms worsened, he went to the Emergency Department, where he tested positive for COVID-19 and influenza B and home quarantine was advised. He had another visit the next day in the same hospital and was given symptomatic treatment. On his fourth visit, due to worsening abdominal pain, he was found to have severe transaminitis and coagulopathy. A CT scan revealed AAC, which was managed conservatively. Treatment with intravenous immunoglobulin (IVIG) therapy led to marked clinical and biochemical improvement within 1 week. CONCLUSIONS This case highlights the importance of early identification of complications associated with COVID-19 and influenza B, as conditions such as acute acalculous cholecystitis can present with atypical symptoms in children, making diagnosis more challenging. Prompt recognition and proper referral from primary care settings are vital to prevent diagnostic delays, ensure effective management, and ultimately improve patient outcomes while preventing further complications.

Indexed as

Acalculous CholecystitisInfluenza, HumanChildCOVID-19HumansImmunoglobulins, IntravenousInfluenza B virusMalePandemicsSARS-CoV-2Tomography, X-Ray ComputedImmunoglobulins, Intravenous

Identifiers

PMID40545682
PMCPMC12203878

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