Sickle cell disease and jawbone osteomyelitis: case report and literature review

Introduction: Sickle cell disease (SCD) can manifest with vaso-occlusive crises (VOC) in various anatomical locations. In this case, a mandibular osteomyelitis developed following a VOC but was initially misdiagnosed due to a lack of specific clinical and radiological indicators. This case report is accompanied by a brief review that highlights potential warning signs shared among similar cases, with the aim of aiding early identification and diagnosis. Observation: A 22-year-old male with SCD of Congolese origin was initially referred to the dental service at Henri Mondor Hospital for facial cellulitis during his hospitalization for a hip vaso-occlusive crisis (VOC). Due to the absence of specific clinical and radiological findings, a dental origin was initially suspected. However, as the patient's condition deteriorated, a diagnosis of mandibular osteomyelitis was eventually established. In addition to antibiotic therapy, a sequestrectomy was performed under general anaesthesia. Delayed healing was observed. Conclusion: Diagnosis osteomyelitis of jawbone in SCD patients can be challenging, as clinical and radiological signs may not always be evident. Dental practitioners and oral surgeons should be vigilant when managing these patients, as complications like mandibular osteomyelitis may present similarly to dental conditions but require prompt investigation and intervention to prevent serious health consequences.

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Publication Details

Journal
Journal of Oral Medicine and Oral Surgery
Published
2025-01-01
DOI
https://doi.org/10.1051/mbcb/2025016
Primary Topic
Hemoglobinopathies and Related Disorders
Type
article
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article

Sickle cell disease and jawbone osteomyelitis: case report and literature review

Bruno Gogly, Rory Durand, Yohann Flottes, Zoé Gaudimier
Journal of Oral Medicine and Oral Surgery
Hemoglobinopathies and Related Disorders
article

Sickle cell disease and jawbone osteomyelitis: case report and literature review

Bruno Gogly, Rory Durand, Yohann Flottes, Zoé Gaudimier
article en

Abstract

Introduction: Sickle cell disease (SCD) can manifest with vaso-occlusive crises (VOC) in various anatomical locations. In this case, a mandibular osteomyelitis developed following a VOC but was initially misdiagnosed due to a lack of specific clinical and radiological indicators. This case report is accompanied by a brief review that highlights potential warning signs shared among similar cases, with the aim of aiding early identification and diagnosis. Observation: A 22-year-old male with SCD of Congolese origin was initially referred to the dental service at Henri Mondor Hospital for facial cellulitis during his hospitalization for a hip vaso-occlusive crisis (VOC). Due to the absence of specific clinical and radiological findings, a dental origin was initially suspected. However, as the patient's condition deteriorated, a diagnosis of mandibular osteomyelitis was eventually established. In addition to antibiotic therapy, a sequestrectomy was performed under general anaesthesia. Delayed healing was observed. Conclusion: Diagnosis osteomyelitis of jawbone in SCD patients can be challenging, as clinical and radiological signs may not always be evident. Dental practitioners and oral surgeons should be vigilant when managing these patients, as complications like mandibular osteomyelitis may present similarly to dental conditions but require prompt investigation and intervention to prevent serious health consequences.

Journal of Oral Medicine and Oral SurgeryVol. 31(3)
Inserm (FR), Université Paris Cité (FR), Hôpitaux Universitaires Henri-Mondor (FR)
Openalex Percentile: Top 79%
Hemoglobinopathies and Related Disorders
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Sickle cell disease and jawbone osteomyelitis: case report and literature review — Bruno Gogly, Rory Durand, et al. · Journal of Oral Medicine and Oral Surgery (2025) | TGRS Research Map | TGRS