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Bilateral Endogenous Bacterial Endophthalmitis and Bacteraemia as the presenting manifestation of Multiple Myeloma. Peter Cikatricis Peter Cikatricis 1, 3 Korina Theodoraki Korina Theodoraki 1 Yit C.Yang Yit C.Yang 3, 4 Alastair K.O. Denniston Alastair K.O. Denniston 1, 2, 3 1 Queen Elizabeth Hospital, University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom 2 Centre for Translational Inflammation Research, University of Birmingham, Birmingham, United Kingdom 3 Wolverhampton Eye Infirmary, Royal Wolverhampton Hospitals NHS Trust, Wolverhampton, United Kingdom 4 Aston University, Birmingham, United Kingdom
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Ocular History 59-year old Caucasian male 12/2013 - 6-day history of painless decrease of vision in both eyes (L > R) Headache, Fever, Nausea and Vomiting POcHx: Left strabismic amblyopia (20/40 BCVA) PMHx: Dental work 2 weeks prior, ex-smoker DHx: Nil
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First Clinical Presentation Bilateral asymmetric vitritis with left panuveitis Fundus infiltrative lesions (OS and ?OD) Systemic signs of infection
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Examination at First Presentation Fever 39.5 °C (103.1°F) Tachycardia 122 bpm Auscultation Grade 4/6 Pan-systolic murmur EYERightLeftBCVA20/40HM A/S & IOP Unremarkable, 12 Ciliary injection, 14 A/C Cells +, Flare + Cells 2-3+, Hypopyon Pupil Reactive/No RAPD PS++ LensClearClear
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Vitreous Few Cells Fundus Roth spots? minimal exudate Right Eye Vitreous Marked vitritis (Grade 4 haze) Fundus Very limited view Left Eye
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Differential Diagnoses Infection: Bacterial Viral HIV/Syphilis Toxoplasmosis Fungal Inflammation: Atypical Sarcoidosis Severe HLA- B27-ass. Masquerade: Lymphoma Other blood malignancies Paraneoplastic
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Initial Investigations Bloodwork (CBC, biochemistry, ESR, CRP, ACE, Ca 2+, ANA, ANCA, TPHA, HIV, Toxoplasma, Borrelia, TB T-Spot) Blood cultures CT/MRI of head and chest Trans-oesophageal Echocardiogram requested
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Lab Results ESR – 62 mm/h (<30) CRP – 246 mg/L (<10) white blood cell count – 14.2 x10 9 /L (4.00-11.00) neutrophils – 12.1 x10 9 /L (2.5–7.5) all serology negative but… Streptococcus Pneumoniae (Serotype 23B) in blood cultures, possible sources: recent dental work bacterial endocarditis
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Transoesophageal echocardiogram: mobile mass at the mitral valve (central on the video below) severe, posteriorly directed jet of mitral regurgitation (light blue flow below) normal Transoesophageal echocardiogram
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Diagnosis Pneumococcus endogenous endophthalmitis Caused by Pneumococcal bacteraemia from endocarditis
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Initial Treatment IV Vancomycin 1g STAT IV Meropenem 1g STAT Intravitreal Vancomycin 2mg – R & L Hospitalised for intravenous antibiotics: IV Vancomycin 1g BD Meropenem 1g TDS In 3 weeks prepared for therapeutic mitral valve replacement – 31mm valve implanted Right Eye Left Eye 20/15 NAD Resolution 20/120 Reduced hypopyon Vitritis - Grade 3 Vitreous haze
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However the story continued... Screening for possible underlying immunosuppression was negative for HIV but.. Elevated paraproteins – 33.2 g/L (>30 g/L) diagnostic of multiple myeloma bone marrow biopsy confirmed: IgG-Multiple Myeloma
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Bone Marrow Biopsy Histopathology Skeletal Survey Low power view of bone marrow High power view of plasma cells CD138 immuno- histochemistry staining of plasma cells Lucencies seen in the proximal femoral shafts, within L5, in the mid-humeral shaft
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Further Treatment 4 weeks after initial presentation discharged from hospital Good cardiac and systemic recovery VA at discharge: 20/15 OD 20/40 OS (recovery of his normal level of vision in amblyopic eye )
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Control after 8 weeks Left eye retinal detachment treated by ppvitrectomy/cryo/gas final visual outcome at 4 months: 20/15 OD 20/80 OS (due for cataract surgery)
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Final Diagnosis Bilateral endogenous pneumococcal endophthalmitis, caused by endocarditis Multiple Myeloma predisposed the patient to develop bacterial endocarditis first case described in the literature
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Conclusion The onset of Multiple Myeloma is often insidious It is of utmost importance to ascertain underlying diagnosis of bilateral endophthalmitis in timely fashion in order to deliver effective treatment Haematological malignancies should be considered as one of the causes of acquired immunosuppression in cases of endogenous endophthalmitis
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