multifocal skeletal tuberculosis mimicking langerhans cell histiocytosis in a child: a case report with a long-term follow-up

conclusions a high index of suspicion is required for the early diagnosis and prompt treatment of patients with osseous tuberculosis. given the high prevalence of tuberculosis in developing countries, tuberculosis should be considered in the differential diagnosis of multifocal lytic lesions and vertebra plana, especially in children. introduction multifocal skeletal tuberculosis is a rare condition that may masquerade as langerhans cell histiocytosis, especially in children. case presentation we report a case of multifocal osseous tuberculosis in a 5-year-old female patient admitted to our hospital with a complaint of low back pain but no history of respiratory symptoms or malaise. radiological findings included vertebra plana and multiple lytic lesions in both the frontal and pelvic bones. an initial diagnosis of langerhans cell histiocytosis was made based on imaging findings; however, the patient underwent further evaluation for mycobacterium tuberculosis, and histopathologic findings confirmed the diagnosis of tuberculosis. the patient showed a nearly complete response after receiving a course of anti-tuberculosis drugs.