Vogt–Koyanagi–Harada disease following BCG vaccination and tuberculosis
© The Author(s). 2016
Received: 28 January 2016
Accepted: 22 April 2016
Published: 12 May 2016
To describe the characteristics, diagnosis, and treatment of the first documented case of Vogt–Koyanagi–Harada (VKH) disease following BCG vaccination (Patient 1) and the first documented case of both VKH disease and tuberculosis (Patient 2).
Two patients were diagnosed with VKH disease and monitored using fundus photography, fundus autofluorescence, fluorescein angiography (FA), spectral-domain optical coherence tomography, and enhanced depth imaging optical coherence tomography (EDI-OCT).
A 39-year-old patient (Patient 1) had bilateral granulomatous anterior uveitis and serous retinal detachment. FA showed multiple punctuate hyperfluorescent lesions and multilobular pools of dye. EDI-OCT revealed serous retinal detachment, subretinal septa, and cystoid spaces. A 40-year-old woman (Patient 2) presented with a 3-week history of decreased vision, headache and tinnitus. Fundus examination showed bilateral disc swelling with serous retinal detachment and retinal folds. She had been diagnosed with tuberculosis. EDI-OCT showed fluctuation of the internal limiting membrane (ILM), retinal folds, retinal pigment epithelial (RPE)-Bruch membrane undulation, choroidal folds, serous retinal detachment. Both of the patients received high dosage of steroid treatment during the diagnosis. A fast recovery in VKH symptoms was observed following the treatment.
Discussion and evaluation
Immunological mechanisms and dysregulation of the immune system may play a significant role in the association between VKH disease and BCG.
EDI-OCT imaging demonstrated structural changes in the photoreceptor layer, RPE-Bruch membrane, choroid, outer retina, ILM in acute VKH.
KeywordsBCG vaccine Serous retinal detachment Tuberculosis Vogt–Koyanagi–Harada disease
Vogt–Koyanagi–Harada (VKH) disease is a rare granulomatous inflammatory disorder affecting the eyes, auditory system, meninges and skin. The precise etiology and pathogenesis of VKH disease are unknown, but current clinical and experimental evidence suggests a cell-mediated autoimmune process driven by T-lymphocytes directed against self-antigens associated with melanocytes in genetically susceptible individuals (Moorthy et al. 1995; Rao 1997). Typical clinical features of VKH include bilateral panuveitis associated with exudative retinal detachment, meningism associated with headache and pleocytosis of cerebrospinal fluid, tinnitus or hearing loss, and cutaneous changes, such as alopecia, poliosis, and vitiligo. Presence of ocular and two or more extraocular features is considered as a complete form of VKH disease. Incomplete VKH disease includes bilateral typical ocular involvement plus either neurologic/auditory or cutaneous changes, whereas probable VKH disease is composed of just ocular manifestations. However, some of these probable VKH patients can develop cutaneous manifestations during the chronic or chronic recurrent stage of the disease. The acute phase of the VKH disease is characterized by bilateral uveitis, diffuse choroidal inflammation, and multifocal serous retinal detachment (Read et al. 2001). During this phase, the neural retina is detached from the retinal pigment epithelium (RPE), the subretinal space is filled with an eosinophilic exudate of proteinaceous material, and the choroid is diffusely infiltrated by lymphocytes, with focal aggregates of epithelioid histiocytes and multinucleated giant cells. These histologic changes during the acute phase have been observed to incur early damage to choroidal melanocytes. Immunohistochemical analysis has also revealed that the choroidal infiltrates observed during this phase are predominantly comprised of T-lymphocytes (Rao 2007).
The chronic phase in which progressive choroidal depigmentation occurs results in a change classically described as sunset glow fundus. During this stage, vitiligo and poliosis may occur (Moorthy et al. 1995; Read et al. 2001), and some patients may develop vision-threatening retinal complications, including choroidal neovascularization and subretinal fibrosis (Read et al. 2001).
Enhanced depth imaging optical coherence tomography (EDI-OCT) and fluorescein angiography (FA) are of great importance in diagnosis of VKH disease, monitoring of morphological changes in the retina and choroid during its course, and evaluation of the efficacy of ophthalmologic therapies (Ishihara et al. 2009). Using EDI-OCT, disruption of the outer retina, especially of the inner/outer segment (IS/OS) junction, and of the cone outer segment tips (COST) line, as well as irregularities of the RPE layer, have been observed in acute VKH disease (Gupta et al. 2009; Vasconcelos-Santos et al. 2010).
Based on these observations, the patient was treated with 1 mg/kg/day of oral prednisone that was gradually tapered off over 6 months.
Patient 2 was a 40-year old darkly pigmently Caucasian female admitted to our clinic in July 2015 complaining of blurred vision in both eyes and optic disc edema. She had been referred by the neurology clinic, which had been monitoring her for the past 3 weeks for complaints of malaise, headache, and tinnitus. Lumbar puncture revealed sterile cerebrospinal fluid lymphocytic pleocytosis. Level of angiotensin-converting enzyme (ACE) was normal; the results of serological testing for syphilis, Lyme disease, herpes simplex virus, varicella zoster virus, cytomegalovirus, and toxoplasma was negative; and brain magnetic resonance imaging was normal. In her previous medical history, she had been diagnosed with tuberculosis and had been treated for 9 months. At diagnosis, her BCVA was 20/50 in the right eye (OD) and 20/32 in the left eye (OS). Slit-lamp biomicroscopy showed bilateral anterior chamber cells. Intraocular pressure was 13 mm Hg OU.
The OCT findings of previous research have confirmed that the densest tissue affected by the inflammatory process in VKH disease is the choroid. Previous studies have also observed that the outer retina, IS/OS junction, RPE, and vitreous are also affected by inflammation (Vasconcelos-Santos et al. 2010; Lee et al. 2009; Zhou et al. 2015). These findings indicate the existence of an immune mechanism against melanocytes accompanied by antigenic peptides accompany and managed by T-lymphocytes (Rao 1997).
Immunotherapy against superficial bladder cancer can be created by administration of BCG vaccine, which triggers a cytokine-mediated inflammatory response leading to the destruction of tumor cells (Uppal et al. 2010).
However, intravesical BCG therapy has been implicated in the development of anterior uveitis in several case reports. The mechanism behind this phenomenon is immune sensitization revealed by BCG with cross-reaction against the ocular antigen. Bilateral panuveitis (Jacob et al. 2006), chorioretinitis (Guex-Crosier et al. 2003), and/or optic neuritis (Hegde and Dean 2005) are rarely seen in patients, and mycobacterial choroiditis has been reported in only two previous case reports (Guex-Crosier et al. 2003).
There are two mechanisms that can be suggested for the origin of ocular inflammation: a local immune response, or a direct choroidal mycobacterial infection as demonstrated by vitreous cultures (Uppal et al. 2010). Burgoyne described the case of a 16-year-old Caucasian girl known not to have tuberculosis or any other systemic disease who developed acute panuveitis that progressed to bilateral serous retinal detachment after undergoing two sessions of purified protein derivative (PPD) skin testing separated by an interval of 8 years (Burgoyne et al. 1991).
A strong T-helper 1 response, which is known to be the most frequent type of immune response associated with uveitis, is induced by M. tuberculosis. Panuveitis is primarily caused by tuberculosis, VKH syndrome, sympathetic ophthalmia, Behcet’s disease, and sarcoidosis.
Uveitis, serous retinal detachment, and VKH may be potentially caused by antigenic mimicry. Investigation of the highest Th1 responses with the sequences of BCG proteins induced by the comparison of the amino acid sequences of retinal proteins and peptides identified several highly similar or even identical regions of 5–11 amino acids. Crossreactivity of the patient’s BCG-specific T cells with retinal autoantigen might have been caused by these epitopes. The previously reported uveitis was presumed to be caused by this phenomenon, referred to as antigenic mimicry (Garip et al. 2009).
BCG toxicity might be an expected result of immune stimulation and it proves that BCG is effective. Role of immune stimulation in the pathogenesis of VKH support this relationship.
EDI-OCT revealed our patients with acute VKH, increased choroidal thickness, RPE-Bruch membrane undulation, fluctuation of ILM, choroidal folds, retinal folds, vertical lining on the outer plexiform layer, increased choroidal hyperreflectivity, serous retinal detachment, Dalen-Fuchs nodules, and subretinal septa. To the best of our knowledge, this is the first report of DF nodules imaged by EDI-OCT in VKH. Previous study revealed focal collections of mononuclear inflammatory cells under elevated mounds of RPE led to the formation of Dalen-Fuchs nodules consisting of lymphocytes, pigment-laden macrophages, epithelioid cells, and proliferated RPE cells (Rao 2007).
The RPE undulation index was first described by Hosoda et al. (2014) and it was observed on the SD-OCT images that patients with VKH disease experienced significant distortions of the RPE layer. This distortion may be due to the choroidal congestion caused by the infiltration of inflammatory cells. Lin et al. (2014) first described the ILM fluctuations observed on the SD-OCT images of acute VKH patients. To the best of our knowledge, patient 2 is the second reported case of ILM fluctuation. Although the mechanism of ILM fluctuation is not fully known, inflammatory cells in vitreous have been hypothesized to cause local constriction of ILM, and retina edema to cause ILM fluctuation (Lin et al. 2014).
Clusters of T-lymphocytes activated around early choroidal melanocytes and macrophages accumulate abnormally and cause extensive choroidal thickening. VKH, in which choroid is the thickest tissue, is one of the main pathologies resulting from this phenomenon. In VKH, a significant increase in hyperreflective points is observed on an area of arterioles and venules, which are the medium choroidal vessels (Nazari et al. 2014). One of the most important findings of OCT in acute VKH disease is the large number of serous retinal detachment areas whose height of these may be much higher than those of serous retinal detachments in other tables. Although the fundus in the right eye of Patient 1 was normal at diagnosis, we found the choroid on EDI-OCT to be thick and observed increased choroidal hyperreflectivity, which indicates the changes concerning the disease. Abnormal increase in choroidal thickness causes fluctuations the RPE-Bruch membrane. The EDI-OCT images revealed that the IS/OS junction and RPE were mainly affected (Lee et al. 2009). These impacts included RPE distortions and disappearance of the IS/OS junction.
The length of the interval from the onset of symptoms to the initiation of the systemic steroid therapy is an important prognostic factor for patients with acute VKH, for whom proper and prompt treatment is crucial. Such treatment may prevent progression of the disease to the chronic recurrent stage and may possibly reduce the incidence and perhaps the severity of extraocular manifestations.
Our findings indicate the importance of considering EDI-OCT findings, which allowed us to identify the histopathologic changes regarding the disease. To the best of our knowledge, patient 1 was the first documented case of VKH following BCG vaccination and patient 2 the first documented case of both VKH disease and tuberculosis. Based on our observations, we hypothesize that immunological mechanisms and dysregulation of the immune system may play a significant role in the association between VKH disease and BCG.
BD writing the article, research concept and design. MKE critical revision of the article, final approval of article. AC collection of data. All authors read and approved the final manuscript.
There is no acknowledgements.
The authors declare that they have no competing interests.
Written informed consent was obtained from the patient for publication of this case report and any accompanying images.
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