Evidence map›Paper›PMID 42021193›Full record

ArticleBMC pediatrics2026

BCG arthritis in a patient with Severe Combined Immunodeficiency Disorder (SCID): a case report.

Shabnam Eskandarzadeh, Zahra Chavoshzadeh, Mohammad Assadi Fanid, Babollah Ghasemi, Amirreza Jabbaripour Sarmadian

Abstract readCase Reports
In one paragraph

Article in BMC pediatrics, 2026. 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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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

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

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No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Shabnam EskandarzadehPediatric Health Research Center, Tabriz University of Medical Sciences, Tabriz, Iran. S_eskandarzadeh@yahoo.com.ORCID 0000-0001-7500-9657
Zahra ChavoshzadehImmunology and Allergy Department, Mofid Children's Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Islamic Republic of Iran.
Mohammad Assadi FanidDepartment of Orthopaedics, Zahra Mardani Azari Children Training, Research and Treatment Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Babollah GhasemiDivision of Clinical Laboratory, Zahra Mardani Azari Children Training, Research and Treatment Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Amirreza Jabbaripour SarmadianPediatric Health Research Center, Tabriz University of Medical Sciences, Tabriz, Iran. amirrjps@gmail.com.ORCID 0000-0001-7677-8458

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSevere combined immunodeficiency (SCID) is a rare group of primary immunodeficiency disorders characterized by profound defects primarily in T cells and, in certain subtypes, in B and NK cells as well. These immune deficiencies predispose affected patients to life-threatening infections and complicate their clinical management. Since the BCG vaccine is routinely administered to neonates in most countries, undiagnosed SCID patients face a significant risk of developing severe localized or disseminated BCG-related complications. Therefore, it should be taken into account in suspicious populations. CASE PRESENTATION: The patient was a 16-month-old Iranian male with JAK3 gene mutation-associated SCID who presented with progressive left elbow swelling, pain, and restricted mobility over 10 days. Physical examination revealed tachycardia, fever, marked swelling and tenderness with severely restricted range of motion, and a firm, fixed, warm palpable mass. Soft tissue ultrasound demonstrated moderate joint effusion with synovial thickening, multiple irregular hypoechoic areas, and increased Doppler vascularity consistent with chronic monoarthritis and periarticular masses of probable bacterial origin. Given the lack of response to empirical therapy and conservative management, surgical excision was performed. Histopathological examination revealed neoplastic spindle cell proliferation with hyperchromatic nuclei, epithelioid macrophages, mixed inflammatory infiltrate, and numerous acid-fast bacilli both intracellularly and extracellularly. To reliably distinguish BCG from other members of the Mycobacterium tuberculosis complex, molecular analysis was performed, which demonstrated deletion of the RD1 region, confirming BCG arthritis. Following surgery and antimycobacterial therapy, the patient demonstrated marked clinical improvement, particularly in elbow range of motion, and was discharged after completing intravenous antibiotics and achieving clinical stabilization.

conclusionsThis case underscores the critical need for revised immunization policies in TB-endemic countries, implementation of systematic neonatal primary immunodeficiency screening programs such as TREC screening, and enhanced healthcare provider awareness regarding the potentially catastrophic consequences of BCG vaccination in immunocompromised populations.

Indexed as

Arthritis, InfectiousBCG VaccineMycobacterium bovisSevere Combined ImmunodeficiencyHumansInfantMaleBCG VaccineArthritisBacillus Calmette Guerin vaccineCase reportSevere combined immune deficiencyTuberculosis vaccine

Identifiers

PMID42021193
PMCPMC13238063

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