Ameh E A, Agada F O, Abubakar A, Aikhionbare H A, Nmadu P T
Department of Surgery, Ahmadu Bello University Teaching Hospital, Zaria, Nigeria.
West Afr J Med. 1999 Jul-Sep;18(3):220-2.
A 3-year old male presented with a 12-month history of painless scalp swellings associated with cough, fever and night sweats. Physical examination showed tender, fluctuant, pulsatile right frontotemporal and temporoparietal masses. Skull radiographs showed osteolytic skull lesions in the frontal and temporal bones. Microscopy of drained caseous material and histology of biopsies from the affected bone edges confirmed tuberculous osteitis. Though there was an initial response to antituberculous agents, the child died after 5 weeks from hepatic failure. Tuberculosis of the skull bones though rare, may become more common with the recent upsurge of tuberculosis worldwide. A high index of suspicion is necessary for early diagnosis and treatment.
一名3岁男性患儿,出现无痛性头皮肿物12个月,伴有咳嗽、发热和盗汗。体格检查发现右侧额颞部和颞顶部有压痛、波动感、搏动性肿块。颅骨X线片显示额骨和颞骨有溶骨性颅骨病变。对引流的干酪样物质进行显微镜检查以及对受累骨边缘活检组织进行组织学检查,证实为结核性骨炎。尽管最初对抗结核药物有反应,但患儿在5周后因肝衰竭死亡。颅骨结核虽然罕见,但随着近期全球结核病发病率的上升,可能会变得更为常见。早期诊断和治疗需要高度的怀疑指数。