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Maja Stojanović

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Open access 2026

"Lupus in fabula": Systemic lupus erythematosus complicated by macrophage activation syndrome with a fatal outcome

Introduction/Objective: Macrophage activation syndrome (MAS) is a hyperinflam-matory syndrome and an extremely rare but potentially life-threatening complication of systemic lupus erythematosus (SLE), other systemic autoimmune and autoinflammatory diseases, infections, and malignancies. Case report: A 33-year-old femal...

Aleksandra Dašić, N. Radovanović, M. Prodanović et al. · 0 citations
Open access Aug 2026

CVID-Associated Enteropathy: Clinical, Biochemical, and Genetic Insights from a Single-Center Cohort

Enteropathy represents one of the most frequent noninfectious clinical manifestations of common variable immunodeficiency (CVID), with underlying pathophysiological mechanisms that remain insufficiently understood. Patients with CVID-associated enteropathy (CVID-E) have a significantly higher frequency of liver inv...

Jelena Ljubicic, Ivan Ranković, U. Karić et al. · 0 citations
Case report Open access Sep 2026

Diagnostic Journey to Granulomatosis with Polyangiitis with Rare Hepatic and Suspected Splenic Involvement: A Case Report

Sarcoidosis and granulomatosis with polyangiitis (GPA) are the most common non-infectious causes of granulomatous lung disease. However, they can sometimes be difficult to distinguish due to overlapping clinical, radiological, and histopathological features. A 54-year-old man was considered to have sarcoidosis in 2018....

Aleksandra Dašić, Dragan Vasin, Maja Stojanović et al. · 0 citations
Open access Aug 2026

Association of CSF2, IL12B, IL23R, TNF, IL6 and IL10 Gene Polymorphisms with Susceptibility to Takayasu Arteritis

The findings support the potential role of IL12B in genetic susceptibility to Takayasu arteritis and suggest possible population-specific genetic effects, while other examined cytokine gene polymorphisms showed no statistically significant association.

Maja Stojanović, Ž. Jovičić, Ana Drazic et al. · 0 citations
Open access Aug 2026

Serum IgM and Soluble IL-2 Receptor as Predictors of Granulomatous-Lymphocytic Interstitial Lung Disease in CVID

Evaluated biomarkers of immunoglobulin (Ig) M and sIL-2R showed a potential role for IgM in disease pathogenesis, and higher sIL-2R levels reinforce the concept of immune dysregulation as a key feature of this CVID phenotype.

Aleksandra Dašić, Rada Mišković, S. Janković et al. · 0 citations
Open access Aug 2026

Persistent Hypogammaglobulinemia Following Anti-CD20 Therapy in a Patient with 22q11.2 Deletion Syndrome: A Case Report

22q11.2 deletion syndrome (22q11.2 DS) is one of the most common microdeletion syndromes, characterized by congenital anomalies and variable immune dysfunction secondary to thymic hypoplasia. The resulting immune dysregulation frequently predisposes affected individuals to autoimmune manifestations, including immun...

Ana Drazic, S. Pasic, Maja Stojanović et al. · 0 citations
Open access Aug 2026

Challenges in Diagnosis and Management of Adult Inborn Errors of Immunity: The Serbian Experience

The experience of the Clinic of Allergy and Immunology at the University Clinical Center of Serbia illustrates not only the broad spectrum of IEI phenotypes managed at a national referral center but also emphasizes the pivotal role of specialized centers in identifying and characterizing ultra-rare cases.

Maja Stojanović · 0 citations

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