Musculoskeletal Tuberculosis occurs in 1%–3% of patients with tuberculosis, and Tuberculous trochanteric bursitis (TTB) is responsible for 1%, assuming it as a rare clinical condition, especially if it occurs in immunocompetent patients. This is a case report about a 51 years old man, with pain in right trochanteric area, without swelling or inflammatory signs, 1 year of evolution. About 20 years ago, he suffered an infected traumatic local hematoma. Ultrasound revealed trochanteric bursitis. He was then submitted to a bursectomy. Histological study revealed chronic necrotizing granulomatous bursitis, with negative Acid-Fast Bacillus (AFB) Tests. After 6 mouths the patient suffer relapse of his complains. The MRI revealed intraosseous edema of the great right trochanter, inflammation of adjacent soft tissues and small infratrochanteric collection. Analytically, CRP of 1.24 mg/dl and positive interferon Gamma. A new bursectomy and curettage were performed with sequestrectomy. Lowestein culture was positive for AFB, it was identified protein MPT64, and a positive DNA Mycobacterium tuberculosis complex research. It was associated medical treatment with antibiotics (12 months). Currently with clinical and imaging improvement, without relapse, after 1 and a half years of follow-up. Usually, TTB arises from the reactivation of an unknown primary infection, whose clinical presentation is often vague, characterized by chronic symptoms. This condition should be considered in the diagnostic discussion whenever a case of recurrent bursitis arises despite the treatment instituted. With the decline in the incidence of tuberculosis, the number of clinical cases of TTB described in the recent literature has decreased considerably, with special attention being given to the reporting and sharing of these cases, with the goal of keeping this diagnosis in perspective in the discussion and orientation of cases of trochanteric bursitis.