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Ref ID: 37617
Ref Type: Journal Article
Authors: Techataweewan, Nawaporn
Mann, Robert W.
Vlok, Melandri
Ruengdit, Sittiporn
Panthongviriyakul, Charnchai
Buckley, Hallie R.
Title: Thalassemia major in a 49-year-old Thai female: Gross and X-ray examination of dry bone
Date: 2021
Source: International Journal of Osteoarchaeology
DOI: 10.1002/oa.3003
Abstract: Objective: We present a clinically diagnosed case of beta thalassemia major in a
deceased 49-year-old Thai female for comparison with paleopathological cases and
consideration of age-related changes of anemic skeletal lesions.
Methods: Dry bone and radiographic descriptions of pathological changes are pro-
vided and compared to clinically documented features of thalassemia.
Results: The limb bones in this case exhibit extreme “ballooning” (widening), cortical
rarefaction (cortex thinning due to osteoporosis), and varus deformity of the proximal
humeri. In the cranium, reduction and coarsening of the trabeculae due to marrow
hyperplasia, and radiographic “hair-on-end” appearance are evident. This individual
did not present with severe porotic hyperostosis or cribra orbitalia but exhibited
diploic expansion.
Significance: This case study provides a rare opportunity for a detailed examination
of the bone changes present in a fatal homozygote with severe anemia. The case also
enables discussion of thalassemia in the wider Southeast Asian context, as major
gene variations are known to impact bone metabolism and possibly cause the devel-
opment of macroscopically observable traits. The absence of observable cribra
orbitalia or severe porotic hyperostosis in such an extreme case calls for careful con-
sideration of age-related skeletal changes in the diagnosis of genetic anemias
(and anemia in general).
Limitations: The individual received blood transfusion treatment that likely prolonged
her life-impacting skeletal progression.
Suggestions for future research: Descriptions of different anatomical cases of thalas-
semia, particularly when accompanied with detailed clinical documentation, would
further enable the development of more rigorous diagnostic protocols that accommodate skeletal variation in disease expression.
Volume: 31
Number: 5
Page Start: 671
Page End: 974