Araújo Juliane Pirágine, Cadavid Ana Maria Hoyos, Lemos Celso Augusto, Trierveiler Marilia, Alves Fabio Abreu
Stomatology Department - School of Dentistry - Universidade de São Paulo, Sao Paulo/SP - Brazil .
Oral Pathology Department - School of Dentistry - Universidade de São Paulo, Sao Paulo/SP - Brazil .
Autops Case Rep. 2015 Sep 30;5(3):55-60. doi: 10.4322/acr.2015.013. eCollection 2015 Jul-Sep.
Sickle cell anemia (SCA) is a hemoglobin disorder that occurs more commonly among Afro-descendants. The authors report the case of a 28-year-old Afro-descendent male patient with the diagnosis of homozygotic sickle cell disease (SCD) referred for evaluation of mandibular lesions. The patient's main complaints included pain and bilateral teeth mobility. An intraoral examination revealed gingiva recession affecting the lower molars with extensive root exposure. A panoramic x-ray showed two radiolucent symmetrical periapical lesions evolving both the first and the second lower molars, bilaterally. The diagnostic hypotheses comprised odontogenic infection, among others. Besides antimicrobial therapy, the two molars of both sides were extracted and bone was collected for histopathological and microbiological analyses. Osteomyelitis was diagnosed, and Streptococcus viridans was recovered from the culture media. Mandibular osteomyelitis should be considered as a diagnosis in patients with SCD. The present case offers an alert to clinicians about the importance of knowing jaw lesions related to SCA.
镰状细胞贫血(SCA)是一种血红蛋白疾病,在非洲裔后代中更为常见。作者报告了一例28岁的非洲裔男性患者,诊断为纯合子镰状细胞病(SCD),因下颌病变评估前来就诊。患者的主要主诉包括疼痛和双侧牙齿松动。口腔检查发现牙龈退缩影响下颌磨牙,牙根广泛暴露。全景X线片显示双侧第一和第二下颌磨牙均有两个对称的透射性根尖周病变。诊断假设包括牙源性感染等。除抗菌治疗外,双侧的两颗磨牙均被拔除,并采集骨组织进行组织病理学和微生物学分析。诊断为骨髓炎,从培养基中培养出草绿色链球菌。对于SCD患者,应考虑下颌骨髓炎的诊断。本病例提醒临床医生注意了解与SCA相关的颌骨病变的重要性。