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Osteomyelitis variolosa, an issue inherited from the past: case report and systematic review.

Authors :
Tang, Jinshuo
Shao, Pu
Liu, Te
Wen, Xinggui
Wang, Yeliang
Wang, Chenyu
Peng, Yachen
Yao, Hua
Zuo, Jianlin
Source :
Orphanet Journal of Rare Diseases; 8/6/2021, Vol. 16 Issue 1, p1-10, 10p
Publication Year :
2021

Abstract

<bold>Background: </bold>Osteomyelitis variolosa is a self-limiting disease triggered by variola virus that cannot be prevented or repaired. Smallpox has been eradicated for 40 years, and complications that remain after smallpox has been cured have become a remarkable diagnostic challenge for contemporary physicians. In this systematic review, we searched PubMed (MEDLINE), Web of Science, and Google Scholar for cases on complications, diagnosis, and treatment for osteomyelitis variolosa between January 1980 and February 2021.<bold>Results: </bold>Ten papers and eleven finished cases, all patients from India, were included for comparison with the present case. In total, 100% of patients presented with bilateral elbow deformities, the ankle was the second most common site of lesion in 50%, and knee lesions accounted for 25% in this study. Flexion contracture, joint instability, secondary arthritis, and fracture are common complications of osteomyelitis variolosa, and most patients receive conservative treatment, while internal fixation has good results for combined fractures.<bold>Conclusions: </bold>Although osteomyelitis variolosa is not a direct threat to the safety of patients, severe skeletal deformities can have a significant impact on quality of life. With advances in surgical techniques, clinicians are offering an increasing number of treatment options for patients with osteomyelitis variolosa. However, most importantly, smallpox has basically been removed from the historical arena, and for areas where smallpox was once endemic, physicians need to deepen the understanding of this disease again. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17501172
Volume :
16
Issue :
1
Database :
Complementary Index
Journal :
Orphanet Journal of Rare Diseases
Publication Type :
Academic Journal
Accession number :
151774560
Full Text :
https://doi.org/10.1186/s13023-021-01985-0