Double challenge: β-thalassaemia caused by a heterozygous pathogenic variant in the HBV gene (c.315+1G>A) and ulcerative colitis in a 12-year-old girl (a rare clinical case)

Authors

DOI:

https://doi.org/10.15574/SP.2025.2(146).134146

Keywords:

ulcerative colitis, β-thalassaemia, anaemia, НВВ (c.315 1G>A) and NOD2 gene mutations, IVS-II-1 (G>A), сhildren

Abstract

Ulcerative colitis (UC) is a chronic inflammatory disease of the intestinal tract with an unknown etiology, characterized by a recurrent course and complications such as anaemia due to iron deficiency, vitamin B12 or B9 deficiencies, or autoimmune haemolysis. β-thalassaemia, an inherited disorder caused by changes in the structure of the β-globin gene (HBB) on chromosome 11, leads to impaired β-chain synthesis in haemoglobin and anaemia of varying severity. The coexistence of these conditions complicates diagnosis and treatment, as symptoms may interact or exacerbate each other. Anaemia in β-thalassaemia can worsen due to chronic blood loss or impaired absorption associated with UC. While UC has occasionally been reported with sickle cell anaemia, its coexistence with β-thalassaemia remains undocumented in the literature.

Aim - to describe a clinical case of a rare combination of UC and β-thalassaemia in a 12-year-old girl.

Clinical case. We report a unique case of UC associated with the NOD2-mutation with extraintestinal manifestations and β-thalassaemia in a 12-year-old girl, caused by a pathogenic heterozygous HBВ mutation (c.315+1G>A) (rs33945777). The patient presented with vomiting, diarrhoea with occasional blood, tenesmus, headaches, weight loss, and hepatosplenomegaly. Hypochromic microcytic anaemia was initially misinterpreted as iron deficiency. UC was diagnosed through clinical signs, colonoscopy, imaging, elevated IgG proteinase 3 antibodies, histopathological findings. β-thalassaemia was confirmed by Next Generation Sequencing (NGS) and Hb-electrophoresis.

Conclusions. The coexistence of UC and β-thalassaemia in a 12-year-old girl represents a rare and complex case. Each of these pathological conditions requires a special multidisciplinary approach to treatment, taking into account the specifics of the disease.

The research was carried out in accordance with the principles of the Helsinki Declaration. The informed consent of the patient was obtained for conducting the studies.

No conflict of interests was declared by the authors.

Author Biographies

O.I. Dorosh, CNP of the Lviv Regional Council "Clinical Center of Children's Medicine", structural subdivision "Western Ukrainian Specialized Center"

Danylo Halytsky Lviv National Medical University, Ukraine

N.S. Trofimova, National Specialized Children's Hospital “OHMATDYT”, Kyiv

SI "National Scientific Center “The M.D. Strazhesko Institute of Cardiology, Clinical and Regenerative Medicine” of the NAMS of Ukraine”, Kyiv

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Published

2025-03-28