A rare case of pulmonary tuberculosis with simultaneous pulmonary and skin sarcoidosis: a case report
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Tuberculosis and sarcoidosis are chronic diseases that rarely occur concomitantly. Sarcoidosis is a multisystem granulomatous disorder characterized pathologically by the presence of non-caseating granulomas in involved tissues. Tuberculosis is infectious disease caused by Mycobacterium tuberculosis characterized by granulomas with caseous necrosis.
We present a case of 43-year-old female refugee from Kosovo with microbiological confirmation of pulmonary tuberculosis and pulmonary and skin sarcoidosis at the same time. Three weeks after corticosteroid therapy for pulmonary sarcoidosis was introduced, positive finding of mycobacterium culture of bronchial aspirate was observed. Based on these results, corticosteroid therapy was excluded and antituberculous therapy was introduced for six months. In the meantime, new nodes on face and nose appeared and skin sarcoidosis was diagnosed. The patient was given corticosteroids and colchicine according to the skin and pulmonary sarcoidosis therapy recommendation.
The authors of this study suggest that in cases when there is a dilemma in diagnosis between tuberculosis and sarcoidosis we should advance with corticosteroid therapy until we have microbiological confirmation of mycobacterium culture. This case is remarkable because this is a third described case of sarcoidosis and tuberculosis together (the first reported in Asia, the second in South Africa), and to authors knowledge, this is a first case report in Europe.
KeywordsTuberculosis Sarcoidosis Corticosteroid Therapy Pulmonary Tuberculosis Chronic Granulomatous Disease
Erythrocyte sedimentation rate
white blood cell
red blood cell
Forced expiratory volume
forced vital capacity
forced expiratory volume
forced expiratory volume in first second
Diffusing capacity of carbon monoxide
High-resolution computed tomography
Mycobacterium Growth Indicator Tube
Polymerase chain reaction.
Tuberculosis and sarcoidosis are chronic granulomatous diseases. In many aspects, they are similar although different. Tuberculosis is infectious disease caused by Mycobacterium tuberculosis (MTB) characterized by granulomas with caseous necrosis, and the treatment is focused on elimination of microorganism. Sarcoidosis is systemic disease of unknown etiology, and is characterized by noncaseous granulomas, therefore it cannot be treated etiologically but immunosuppressive as a systemic immunological disease [1, 2]. Overall mortality from sarcoidosis is 1-5% usually from respiratory, cardiac or central nervous system disease . The histological similarity between sarcoidosis and tuberculosis (with epithelioid cell granulomas as the typical common finding) has stimulated the search for an association between mycobacterium and sarcoidosis, and it has been hypothesized that sarcoidosis could be a separate manifestation of infection with mycobacterium . These diseases occur concomitantly very rarely [4, 5]. Less commonly, tuberculosis develops as an opportunistic infection in patients following corticosteroid treatment for sarcoidosis.
In this very rare case of 43 years-old female, refugee from Kosovo, was admitted as an outpatient to the Department of pulmonary diseases in 2003. because of erythema nodosum and dry cough. She was without fever during admission, smoked up to 30 cigarettes daily and was healthy most of her life. She suffered only of head injury and face trauma acquired during the war (during 1995.) by shelling. Three years before the outbreak of erythema nodosum, two small red subcutaneous tubercles were found on her forehead, in the left eyebrow area. The biopsy test showed chronic granulomatous infection that was described as a reaction to a foreign body.
Microbiological examinations of the skin substrata in direct microscopy and polymerase chain reaction (PCR) with specific primer had not confirmed presence of M. tuberculosis. After 6 months of the beginning of ATL treatment, the patient received corticosteroid (prednisolone 40 mg daily) and colchicine therapy (200 mg daily) for lung and skin type of sarcoidosis. After four months of the corticosteroid therapy chest radiogram showed almost complete regression of nodular infiltrates in lung parenchyma. The skin changes were considerably smaller, dry on surface, and there were no new lesions on the skin while ACE was in normal rate (30 U/l).
A rare case of skin and lung sarcoidosis with positive mycobacterium culture obtained from bronchial aspirate has been presented. Sarcoidosis is a common multisystem granulomatous disease that frequently involves the lungs and can result in pulmonary fibrosis . Based on positive finding of the bronchial aspirate, the diagnosis of lung TB was confirmed. According to authors' knowledge there has not been described a case with positive culture on MTB obtained from bronchial aspirate and with noncaseous granulomas in lung parenchyma, bronchial wall and skin. Pathohistological findings of lung and bronchial wall suggested on sarcoidosis, but confusing fact was positive tuberculosis skin test, although it can be positive in the cases of sarcoidosis. Recent innovative blood tests that measure the cell-mediated immune response of TB-infected individuals like quantiferon test are highly specific for detecting M. tuberculosis infection and may be helpful in diagnostic evaluations in conjuction with risk assessment and radiography . At the time of patient admission, we did not use quantiferon-TB Gold test yet.
In the last 20 years, the research papers have recorded detection of mycobacterial DNA in some sarcoide lesions, especially in lymph nodes that indicates possible connection between these two diseases [7, 8, 9, 10, 11]. Silent asymptomatic stage I of sarcoidosis complicated with pulmonary tuberculosis has been recent published .
Sarcoidosis may presents with a wide range of symptoms. Noncaseating epitheloid cell granulomas characterizing sarcoidosis may affect most organs, including the skin. Skin lesions may be the only manifestations, or just one of several other organ involvements. Cutaneous lesions are present in ~25% of sarcoidosis patients . The skin lesions could have specific aspects (papules, plaques, nodules, alopecia or purple scars) or can be more or less nonspecific (erythema nodosum) . In the Netherlands epidemiological study sarcoidosis was mostly associated with rheumatoid arthritis .
The presented case has been of clinical interest because it happens very rarely that pulmonary tuberculosis and lung sarcoidosis coincide in the same patient with noncaseous lung granulomas. The dilemma was present only because Mantoux test (skin test) was positive. In the former states of Yugoslavia tuberculosis skin test was positive in more than 95% of population because bacillus Calmette-Guerin vaccination (BCG vaccine) was compulsory. It had to be carried out just after birth and then three times until a person was 18 years old. In spite of vaccination, inhabitants can come in touch with the infected persons, and it happened more often during the war in Croatia (1991.-1995.) and another parts of former Yugoslavia, because of the migration of the population from other parts of the Balkan (refugees, fugitives from Bosnia and Kosovo) where the incidence of lung tuberculosis was very high, comparing to Croatia (Kosovo 80/100000, Southern Croatia 18-20/100 000).
In the Sothern Croatia ratio of tuberculosis and sarcoidosis is 1:10 . During ATL therapy complete regressions of new infiltrates in the upper lobe without mycronodular infiltrates has been achieved. Skin sarcoidosis was pathohistological confirmed, with negative direct smear microscopy examination in Ziehl-Neelsen stain and absence of mycobacterium DNA in skin granulomas.
Absence of mycronodular infiltrates (granulomas) in lung parenchyma and reduced changes of skin during 4 months of corticosteroid therapy have additionally proved the diagnosis of sarcoidosis with M. tuberculosis positive lung tuberculosis. Three years before sarciodosis and tuberculosis had been diagnosed, skin forehead granuloma was verified which was explained as granuloma of a foreign body due to previous injuries at shelling. However, according to this study, skin sarcoidosis cannot be excluded at that time. If the bronchial aspirate had not been sent for microbiological testing and if the therapy with corticosteroid had continued, a severe type of lung TB with cavities and probably galloping tuberculosis would have been developed. This particular represented case suggests us if suspicion of tuberculosis is high (for example when the patient had a tuberculin test of 14 mm, a cavity 8 × 12 mm in the apical-posterior segment of the upper left lobe and purulent secretion from the left upper lobe bronchus on bronchoscopy) the ATL treatment can start immediately. In the cases when patient's condition is rapidly deteriorating, corticosteroids and antituberculosis therapy could be started concurrently, until microbiological confirmation is established.
In cases when there is a dilemma in diagnosis between tuberculosis and sarcoidosis, we should advance with corticosteroid therapy until we have microbiological confirmation of mycobacterium culture . In this particular case the doubt has been present from the very beginning, because of the positive skin test and data of previous living place where the incidence of tuberculosis is still high.
We have presented the case of a patient with microbiological confirmation of pulmonary tuberculosis and pulmonary and skin sarcoidosis at the same time and have emphasized the diagnostic dilemmas that may occur when these conditions coexist. The beginning of steroid therapy in patients with underlying infection may accentuate life-threatening complications. The proper evaluation of all relevant findings and case-history data needs to be considered. The authors suggest that in cases when there is a dilemma in diagnosis between tuberculosis and sarcoidosis we should advance with corticosteroid therapy until we have microbiological confirmation of mycobacterium culture.
Written informed consent was obtained from the patient for publication of this case report and accompanying images. A copy of the written consent is available for review by editor-in-chief of this journal.
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