[Rare case of multifocal tuberculosis in Burkina Faso in a sickle cell SC patient with an atypical location: the sternoclavicular joint].

Medecine tropicale et sante internationale Pub Date : 2024-08-28 eCollection Date: 2024-09-30 DOI:10.48327/mtsi.v4i3.2024.506
Yannick Laurent Tchenadoyo Bayala, Ismaël Ayouba Tinni, Fulgence Kaboré, Marcellin Bonkoungou, Wendlassida Joëlle Stéphanie Zabsonré, Dieu-Donné Ouedraogo
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Abstract

Introduction: Tuberculosis and sickle cell disease are common in sub-Saharan Africa. Multifocal tuberculosis, more common in immunocompromised patients, is rare in SC sickle cell patients, especially when localized to the sternoclavicular joint.

Case report: A 44-year-old male sickle cell patient, black African, of Burkina Faso origin, with no other pathological history, presented with chronic inflammatory low back pain associated with right-sided inflammatory gonalgia and hacking cough. This symptomatology had been developing for 7 months in the context of fever and altered general condition. Examination revealed oligoarthritis of the right sternoclavicular joint and the left knee associated with pulmonary condensation syndrome and pleural effusion, a cold abscess in the right sternoclavicular joint, and a purulent fistulized right inguinal adenopathy. Biology revealed a biologic inflammatory syndrome. The GeneXpert test was positive in sputum, with no resistance to rifampin. Intradermal tuberculin test was positive. Chest CT revealed right sternoclavicular osteoarthritis and lumbar CT revealed L3-L4 spondylodiscitis. A standard radiograph of the left knee showed signs of arthritis. The diagnosis was tuberculosis with multifocal bone, pleural, and lymph node involvement. The patient was started on standard analgesics and antituberculosis drugs. The course was favorable.

Conclusion: Multifocal tuberculosis may affect SC sickle cell patients and requires vigilance to prevent complications, especially in rare articular localizations such as the sternoclavicular joint.

导言:结核病和镰状细胞病在撒哈拉以南非洲很常见。多灶性肺结核在免疫力低下的患者中更为常见,但在镰状细胞病患者中却很罕见,尤其是胸锁关节部位的多灶性肺结核:病例报告:一名 44 岁的男性镰状细胞患者,非洲黑人,布基纳法索血统,无其他病史。在发热和全身状况改变的情况下,这种症状已经持续了 7 个月。检查发现右胸锁关节和左膝关节少关节炎,伴有肺凝结综合征和胸腔积液,右胸锁关节有冷脓肿,右腹股沟腺病有化脓性瘘管。生物学检查显示患者患有生物炎症综合征。痰中的基因Xpert检测呈阳性,对利福平无抗药性。皮内结核菌素试验呈阳性。胸部 CT 显示右胸锁关节骨关节炎,腰椎 CT 显示 L3-L4 椎间盘炎。左膝的标准X光片显示有关节炎的迹象。诊断结果为结核病,多灶性骨骼、胸膜和淋巴结受累。患者开始服用标准止痛药和抗结核药物。病程顺利:结论:多灶性结核可能会影响南卡罗来纳州镰状细胞患者,需要提高警惕以预防并发症,尤其是在胸锁关节等罕见的关节部位。
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