Primary Tubercular Osteomyelitis Of The Sternum: Report of Two cases
S Bajracharya, G Singh, M Singh
Keywords
sternal tuberculosis, tubercular osteomyelitis
Citation
S Bajracharya, G Singh, M Singh. Primary Tubercular Osteomyelitis Of The Sternum: Report of Two cases. The Internet Journal of Third World Medicine. 2006 Volume 5 Number 2.
Abstract
Tubercular involvement of the sternum, leading to osteomyelitis, is a rarely described entity even in countries where tuberculosis is endemic. Frank Presentation of this entity is even more uncommon. We describe two cases who presented with discharging sinuses with erythematous lesion over the sternum with constitutional symptoms like fever, loss of appetite and significant weight loss, but without features of pulmonary tuberculosis like cough, hemoptysis. Plain Radiographs demonstrated eroding cortex of the manubrium with lytic lesion. Tubercular etiology was suggested by presence of epithelioid granulomas and acid fast bacilli in the Ziehl-Neelsen staining of the aspirate from the lesion. Both patients responded well to antitubercular treatment.
Introduction
Tuberculosis remains a formidable challenge to health care providers in developing countries. Sternal osteomyelitis is a rarely described manifestation of tuberculosis. We report an unusual cases of sternal tubercular osteomyelitis treated with Anti tubercular regimen of 12 months duration.
Case 1
A 35-year-old male, from Sarlahi, a Terai district of Eastern Nepal, presented with complaints of a discharging sinus with redness on the anterior chest wall, over the manubrium, noticed to be present over the last 3 months. He also had low grade fever, with evening rise, and anorexia of 3 months duration. There was no history of cough, expectoration or chest pain; and no significant family history.
On examination, he was afebrile, weighed 50 kg. A 4 X 4 cm erythematous lesion with discharging sinus was present over the distal part of the sternum and another discharging sinus just distal and right part of anterior chest wall as shown in Fig 1 (a). There was no significant lymphadenopathy. Systemic examination revealed no abnormalities.
Investigations revealed a decreased hematocrit and lymphocytosis. The ESR was elevated at 48mm/hr. Chest X-ray PA view was normal, however the lateral film revealed cortical breach and irregularity of the xiphisternum along with a lytic lesion as shown in Fig 1 (b). Contrast enhanced computed tomography (CT) of the chest was advised, but deferred because of ecomomic problems of patient. Ultrasonography of the abdomen was normal. The fine needle aspiration cytology (FNAC) from the affected area revealed numerous epithelioid cell granulomas with mononuclear infiltrate and scattered giant cells. Ziehl-Neelsen staining of the aspirate was positive for acid fast bacilli. HIV serology was negative.
The patient was started on antitubercular treatment with four drugs: isoniazid, rifampicin, ethambutol and pyrazinamide. After 2 weeks of the treatment, his appetite improved with decrease in discharge. After 1 months of treatment, the erythema had subsided, and the patient had also gained weight. After 3 months of treatment, discharging sinus was healed completely. He was switched over to continuation phase with 3 drugs: isoniazid, rifampicin and pyrazinamide which were continued for another 9 months. The patient was completely cured with total 12 months of Antitubercular drugs.
Case 2
A 57-year-old male, from Pachthar, a remote hilly village of Eastern Nepal presented with complaints of a discharging sinus with redness on the anterior chest wall with multiple ulcerating lesion over the manubrium for 5 and half months duration. Fig 2 (a) Constitutional symptoms like low grade fever, with evening rise, and anorexia was present for last three months. As in previous case, there was no history of cough, expectoration or chest pain; and no significant family history.
On examination, he was febrile, weighed 47 kg. A 7 X 10 cm erythematous lesion with multiple discharging sinuses and ulceration was present over the whole of the sternum extending from suprasternal notch to xiphisternum. No significant lymphadenopathy was detected. Systemic examination was within normal limit.
Investigations revealed a normal hemogram. The ESR was elevated at 60mm/hr. Chest X-ray PA view was normal, however the lateral film revealed a lytic lesion on the proximal part of the sternum with cortical breach. Ultrasonography of the abdomen was normal. The fine needle aspiration cytology (FNAC) from the site was suggestive of tuberculosis as previous one.
Antitubercular treatment with four drugs: isoniazid, rifampicin, ethambutol and pyrazinamide was started according to body weight. After 2 months of treatment, the erthema had decreased to some extent with decreased amount in discharge. After 3 months of treatment, erythema and discharging sinus were healed completely. Continuation phase with 3 drugs: isoniazid, rifampicin and pyrazinamide were continued for another 9 months. The patient was satisfied with total 12 months of Antitubercular drugs.
Discussion
Osteomyelitis of the sternum is a very rare manifestation of tuberculosis. Around 25 cases have been reported so far, in the post antitubercular treatment era. Davies et al reported that, out of more than 4000 patients with tuberculosis, only 2 had sternal tuberculosis1. The condition is even more uncommon in children. Out of 20 cases of sternal osteomyelitis reviewed by McLellan et al, only 2 were children2. The earliest age at presentation has been 9 months, described in a Japanese infant3. From India, a few cases of sternal tuberculosis have been described in adults 4,5, 6. Ray et al have described a case of disseminated tuberculosis in a child, in which the sternum was also involved7.
Tubercular sternal osteomyelitis is usually caused by reactivation of latent loci formed during hematogenous or lymphatic dissemination of primary tuberculosis8. Direct extension from contiguous mediastinal lymph nodes has also been described9. Unlike pyogenic sternal infections characterized by more rapid and fulminant course, tubercular sternal osteomyelitis usually presents insidiously as swelling and pain over the sternum2. Constitutional symptoms are relatively uncommon.
Concomitant extrasternal tubercular involvement was described in 8 out of 20 cases reviewed by McLellan et al2. These included mediastinal lymph nodes (5), paraspinal abscess (2), and pulmonary involvement (1). We could not find any extrasternal source of infection in our patient.
Definitive diagnosis rests largely with the histological and microbiological examination of sternal tissue. Needle aspiration, as compared to surgical exploration, is less invasive and may represent the diagnostic procedure of first choice. However, it demonstrates positive cultures less frequently than excisional biopsy2.
CT chest, apart from the evaluation of the sternum, is also helpful in detecting any pulmonary or mediastinal involvement, which may be missed on plain Chest X-ray2, 9. Recently the role of MRI has been studied in evaluation of sternal tuberculosis. MRI is helpful in picking up bone marrow involvement and peristernal soft tissue changes10.
In addition to tuberculosis, the differential diagnosis of a chest wall discharging sinuses includes pyogenic infections, malignancy, sarcoidosis, actinomycosis, and fungal disease9. FNAC or needle biopsy is useful to confirm the presence of tuberculosis or exclude other conditions.
There is no consensus on the optimal treatment of sternal tuberculosis. Although some authors suggest that medical treatment alone is effective, others believe that aggressive debridement with primary closure as an adjunct to chemotherapy is needed to prevent recurrence or the formation of a draining sinus11. Our patients responded well to medical treatment. However, close follow up is needed in these patients to determine whether surgical treatment will ultimately be needed.
Correspondence to
Dr Suraj Bajracharya, MBBS, MS (Orthopaedics) Department of Orthopaedics B P Koirala Institute of Health Sciences Dharan, Nepal E-mail: drsurajbajra@yahoo.com