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Solitary Choroidal Tuberculoma in an Immunocompetent Patient

Solitary Choroidal Tuberculoma in an Immunocompetent Patient We report a case of choroidal tuberculoma in an immunocompetent patient who was referred to us with the possible diagnosis of choroidal melanoma. Findings from routine investigations failed to identify systemic tuberculosis infection. Visual improvement and choroidal tuberculoma involution to a flat inactive scar can occur with proper and rapid diagnosis and treatment. Report of a Case A 24-year-old Guinean man living in Belgium for the last 6 months was referred to our hospital with a 10-day history of decreased vision in the left eye. He was of poor socioeconomic status and had no significant medical history, had not been exposed to tuberculosis, and had not received the bacille Calmette-Guérin vaccine. His visual acuity was 20/20 OD and 20/400 OS. Anterior segment examination findings from both eyes were within normal limits and did not reveal cell or flare. The right eye was normal on funduscopic examination. In the left eye, a 5-mm-diameter yellow choroidal mass was bisecting the foveola (Figure 1). Discrete vitreous inflammatory reaction was present. Fluorescein angiography findings demonstrated early heterogeneous blockage and late staining of the lesion. Results of B-scan ultrasonography showed a thick, dome-shaped choroidal lesion with a 4.8-mm irregular low-to-medium internal reflectivity. The differential diagnosis included infectious or inflammatory granuloma (sarcoidosis, tuberculosis), Toxocara, fungal disease, lymphoma, and choroidal metastasis. Amelanotic choroidal melanoma was not considered because it is uncommon in African patients. Figure 1. View LargeDownload Choroidal mass bisecting the fovea. Complete physical examination and medical evaluation findings, including a chest x-ray film, were normal. Results of a blood uveitis workup (serum angiotensin converting enzyme, serum lysozyme, fluorescent titer antibody, antibody screen, VDRL [Venereal Disease Research Laboratory] titer, Toxoplasma titer, Toxocara titer, Lyme titer, and cultures) were negative. Cultures of sputum and urine also yielded negative results. Test results for human immunodeficiency virus were negative. A purified protein derivative skin test was highly positive (induration, 25 mm). We made the clinical diagnosis of solitary choroidal tuberculoma in an immunocompetent patient in whom routine investigations failed to identify systemic tuberculosis infection. The patient was started on isoniazid, rifampin, and ethambutol for a 6-month period. The choroidal granuloma subsequently decreased in size over the following 6 months to form a flat chorioretinal scar (Figure 2). Visual acuity improved to 20/200 OS. Figure 2. View LargeDownload Flat choroidal scar 6 months after antituberculosis therapy. Comment Ocular tuberculosis involving any tissue of the eye is a rare event (1% of all cases of tuberculosis).1,2 Most patients with ocular involvement have no history of pulmonary or systemic forms of tuberculosis, and 50% have normal findings on chest x-ray.1,2 Ocular manifestations associated with tuberculosis are either caused by an active infection or an immunologic reaction (delayed hypersensitivity) in the absence of any infectious agent. Choroidal infection is the most common ocular manifestation during dissemination of the bacillus via the blood stream. Choroidal tubercles are frequently unilateral and appear predominantly in the posterior pole as solitary or multiple amelanotic lesions.1-5 They may manifest with or without active tuberculosis. To our knowledge, only 4 other cases of a choroidal tuberculoma without systemic evidence of tuberculosis and normal chest radiograph findings have been reported.3-5 Purified protein derivative skin test results were positive in 2 cases.3,4 The third case was confirmed after histopathological examination of the enucleated eye.5Mycobacteriumtuberculosis DNA amplification by polymerase chain reaction on aqueous humor sample confirmed the diagnosis in the fourth case.5 Ocular diagnosis is generally presumptive and is based primarily on clinical appearance, systemic evaluation, and response to treatment. The angiographic and ultrasonographic features can assist in excluding other diagnoses (eg, amelanotic choroidal melanoma, choroidal metastasis).2-5 Histopathologic confirmation from ocular tissues is uncommon and difficult to obtain. Molecular diagnosis of tuberculosis by polymerase chain reaction has been recently applied to detect M tuberculosis from aqueous humor or vitreous with interesting results.1,2 Positive purified protein derivative skin test results do not indicate a systemic tuberculosis infection, but this is the first test performed in the investigation of a patient in whom tuberculosis is suspected. The size of the reaction, contact history, regional prevalence of atypical mycobacteria, and patient characteristics such as age and immune status should be taken into consideration while interpreting the result of a purified protein derivative skin test.1 Nevertheless, all individuals with reaction sizes greater than 22 mm were found to be infected with M tuberculosis, regardless of contact history.1 Most patients with ocular tuberculosis require systemic therapy, and isoniazid, rifampin, pyrazinamide, ethambutol, and streptomycin are the principal antituberculosis drugs. Protocol for treating ocular tuberculosis is similar to that for pulmonary tuberculosis and should be adapted to the immune status of the patient. Visual recovery and choroidal tuberculoma involution to a flat inactive scar can occur with proper and rapid diagnosis and treatment.3-5 Correspondence: Dr De Potter, Ocular Oncology Unit, Cliniques Universitaires St-Luc, 10 Avenue Hippocrate, 1200 Brussels, Belgium (depotter@ofta.ucl.ac.be). Financial Disclosure: None. References 1. Helm CJHolland GN Ocular tuberculosis. Surv Ophthalmol 1993;38229- 256PubMedGoogle ScholarCrossref 2. Bodaghi BLeHoang P Ocular tuberculosis. Curr Opin Ophthalmol 2000;11443- 448PubMedGoogle ScholarCrossref 3. Mansour AMHaymond R Choroidal tuberculomas without evidence of extraocular tuberculosis. Graefes Arch Clin Exp Ophthalmol 1990;228382- 383PubMedGoogle ScholarCrossref 4. Berinstein DMGentile RCMcCormick SAWalsh JB Primary choroidal tuberculoma. Arch Ophthalmol 1997;115430- 431PubMedGoogle ScholarCrossref 5. Sarvananthan NWiselka MBibby K Intraocular tuberculosis without detectable systemic infection. Arch Ophthalmol 1998;1161386- 1388PubMedGoogle Scholar http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Archives of Ophthalmology American Medical Association

Solitary Choroidal Tuberculoma in an Immunocompetent Patient

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References (5)

Publisher
American Medical Association
Copyright
Copyright © 2005 American Medical Association. All Rights Reserved.
ISSN
0003-9950
eISSN
1538-3687
DOI
10.1001/archopht.123.6.864
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Abstract

We report a case of choroidal tuberculoma in an immunocompetent patient who was referred to us with the possible diagnosis of choroidal melanoma. Findings from routine investigations failed to identify systemic tuberculosis infection. Visual improvement and choroidal tuberculoma involution to a flat inactive scar can occur with proper and rapid diagnosis and treatment. Report of a Case A 24-year-old Guinean man living in Belgium for the last 6 months was referred to our hospital with a 10-day history of decreased vision in the left eye. He was of poor socioeconomic status and had no significant medical history, had not been exposed to tuberculosis, and had not received the bacille Calmette-Guérin vaccine. His visual acuity was 20/20 OD and 20/400 OS. Anterior segment examination findings from both eyes were within normal limits and did not reveal cell or flare. The right eye was normal on funduscopic examination. In the left eye, a 5-mm-diameter yellow choroidal mass was bisecting the foveola (Figure 1). Discrete vitreous inflammatory reaction was present. Fluorescein angiography findings demonstrated early heterogeneous blockage and late staining of the lesion. Results of B-scan ultrasonography showed a thick, dome-shaped choroidal lesion with a 4.8-mm irregular low-to-medium internal reflectivity. The differential diagnosis included infectious or inflammatory granuloma (sarcoidosis, tuberculosis), Toxocara, fungal disease, lymphoma, and choroidal metastasis. Amelanotic choroidal melanoma was not considered because it is uncommon in African patients. Figure 1. View LargeDownload Choroidal mass bisecting the fovea. Complete physical examination and medical evaluation findings, including a chest x-ray film, were normal. Results of a blood uveitis workup (serum angiotensin converting enzyme, serum lysozyme, fluorescent titer antibody, antibody screen, VDRL [Venereal Disease Research Laboratory] titer, Toxoplasma titer, Toxocara titer, Lyme titer, and cultures) were negative. Cultures of sputum and urine also yielded negative results. Test results for human immunodeficiency virus were negative. A purified protein derivative skin test was highly positive (induration, 25 mm). We made the clinical diagnosis of solitary choroidal tuberculoma in an immunocompetent patient in whom routine investigations failed to identify systemic tuberculosis infection. The patient was started on isoniazid, rifampin, and ethambutol for a 6-month period. The choroidal granuloma subsequently decreased in size over the following 6 months to form a flat chorioretinal scar (Figure 2). Visual acuity improved to 20/200 OS. Figure 2. View LargeDownload Flat choroidal scar 6 months after antituberculosis therapy. Comment Ocular tuberculosis involving any tissue of the eye is a rare event (1% of all cases of tuberculosis).1,2 Most patients with ocular involvement have no history of pulmonary or systemic forms of tuberculosis, and 50% have normal findings on chest x-ray.1,2 Ocular manifestations associated with tuberculosis are either caused by an active infection or an immunologic reaction (delayed hypersensitivity) in the absence of any infectious agent. Choroidal infection is the most common ocular manifestation during dissemination of the bacillus via the blood stream. Choroidal tubercles are frequently unilateral and appear predominantly in the posterior pole as solitary or multiple amelanotic lesions.1-5 They may manifest with or without active tuberculosis. To our knowledge, only 4 other cases of a choroidal tuberculoma without systemic evidence of tuberculosis and normal chest radiograph findings have been reported.3-5 Purified protein derivative skin test results were positive in 2 cases.3,4 The third case was confirmed after histopathological examination of the enucleated eye.5Mycobacteriumtuberculosis DNA amplification by polymerase chain reaction on aqueous humor sample confirmed the diagnosis in the fourth case.5 Ocular diagnosis is generally presumptive and is based primarily on clinical appearance, systemic evaluation, and response to treatment. The angiographic and ultrasonographic features can assist in excluding other diagnoses (eg, amelanotic choroidal melanoma, choroidal metastasis).2-5 Histopathologic confirmation from ocular tissues is uncommon and difficult to obtain. Molecular diagnosis of tuberculosis by polymerase chain reaction has been recently applied to detect M tuberculosis from aqueous humor or vitreous with interesting results.1,2 Positive purified protein derivative skin test results do not indicate a systemic tuberculosis infection, but this is the first test performed in the investigation of a patient in whom tuberculosis is suspected. The size of the reaction, contact history, regional prevalence of atypical mycobacteria, and patient characteristics such as age and immune status should be taken into consideration while interpreting the result of a purified protein derivative skin test.1 Nevertheless, all individuals with reaction sizes greater than 22 mm were found to be infected with M tuberculosis, regardless of contact history.1 Most patients with ocular tuberculosis require systemic therapy, and isoniazid, rifampin, pyrazinamide, ethambutol, and streptomycin are the principal antituberculosis drugs. Protocol for treating ocular tuberculosis is similar to that for pulmonary tuberculosis and should be adapted to the immune status of the patient. Visual recovery and choroidal tuberculoma involution to a flat inactive scar can occur with proper and rapid diagnosis and treatment.3-5 Correspondence: Dr De Potter, Ocular Oncology Unit, Cliniques Universitaires St-Luc, 10 Avenue Hippocrate, 1200 Brussels, Belgium (depotter@ofta.ucl.ac.be). Financial Disclosure: None. References 1. Helm CJHolland GN Ocular tuberculosis. Surv Ophthalmol 1993;38229- 256PubMedGoogle ScholarCrossref 2. Bodaghi BLeHoang P Ocular tuberculosis. Curr Opin Ophthalmol 2000;11443- 448PubMedGoogle ScholarCrossref 3. Mansour AMHaymond R Choroidal tuberculomas without evidence of extraocular tuberculosis. Graefes Arch Clin Exp Ophthalmol 1990;228382- 383PubMedGoogle ScholarCrossref 4. Berinstein DMGentile RCMcCormick SAWalsh JB Primary choroidal tuberculoma. Arch Ophthalmol 1997;115430- 431PubMedGoogle ScholarCrossref 5. Sarvananthan NWiselka MBibby K Intraocular tuberculosis without detectable systemic infection. Arch Ophthalmol 1998;1161386- 1388PubMedGoogle Scholar

Journal

Archives of Ophthalmology – American Medical Association

Published: Jun 1, 2005

Keywords: immunocompetence,tuberculoma

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