Maxillary recontouring in transfusion-dependent β-thalassemia major: A case for virtual surgical planning and navigation

Transfusion-dependent β-thalassemia (TDT), historically known as β-thalassemia major, is a monogenic disorder characterized by ineffective erythropoiesis and progressive skeletal deformity due to expansion of the bone marrow. Maxillofacial changes, including midfacial hyperplasia and malocclusion, result from chronic anemia-driven extramedullary hematopoiesis and can lead to significant functional and psychosocial morbidity. While systemic therapies continue to evolve, few reports describe modern surgical correction of craniofacial deformities. We present a digitally planned, guide-assisted maxillary recontouring in a patient with TDT and severe maxillary hyperplasia, emphasizing the role of virtual surgical planning (VSP) and intraoperative navigation. • Case of transfusion-dependent β-thalassemia with severe maxillary hyperplasia. • Digitally planned, guide-assisted maxillary recontouring performed successfully. • Virtual surgical planning enabled precision in craniofacial deformity correction. • Intraoperative navigation improved accuracy despite compromised bone quality.

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Publication Details

Journal
Oral and Maxillofacial Surgery Cases
Published
2025-12-07
DOI
https://doi.org/10.1016/j.omsc.2025.100431
Primary Topic
Hemoglobinopathies and Related Disorders
Type
article
Field-Weighted Citation Impact
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article

Maxillary recontouring in transfusion-dependent β-thalassemia major: A case for virtual surgical planning and navigation

Oral and Maxillofacial Surgery Cases
Hemoglobinopathies and Related Disorders
article

Maxillary recontouring in transfusion-dependent β-thalassemia major: A case for virtual surgical planning and navigation

article en

Abstract

Transfusion-dependent β-thalassemia (TDT), historically known as β-thalassemia major, is a monogenic disorder characterized by ineffective erythropoiesis and progressive skeletal deformity due to expansion of the bone marrow. Maxillofacial changes, including midfacial hyperplasia and malocclusion, result from chronic anemia-driven extramedullary hematopoiesis and can lead to significant functional and psychosocial morbidity. While systemic therapies continue to evolve, few reports describe modern surgical correction of craniofacial deformities. We present a digitally planned, guide-assisted maxillary recontouring in a patient with TDT and severe maxillary hyperplasia, emphasizing the role of virtual surgical planning (VSP) and intraoperative navigation. • Case of transfusion-dependent β-thalassemia with severe maxillary hyperplasia. • Digitally planned, guide-assisted maxillary recontouring performed successfully. • Virtual surgical planning enabled precision in craniofacial deformity correction. • Intraoperative navigation improved accuracy despite compromised bone quality.

Oral and Maxillofacial Surgery CasesVol. 12(1)
The University of Texas at San Antonio Health Science Center (US), The University of Texas at San Antonio (US)
Good health and well-being
Openalex Percentile: Top 29%
Hemoglobinopathies and Related Disorders
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