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Orbital Pseudotumor with Wegener's Granulomatosis Developing Antiphospholipid Syndrome
Authors: Tatiana Rosca, MD, PhD, * Cristina Tanaseanu, MD,PhD,** Codruţ Sarafoleanu, MD, PhD, *** Ana Tatiana Şerban, MD **** *Emergency Clinical Hospital St.Pantelimon , Neurosurgery Departmnet, Bucharest, Romania ** Emergency Clinical Hospital St.Pantelimon, Internal Medicine Department, Bucharest, Romania *** Clinical Hospital Sf.Maria, ENT Department, Bucharest, Romania ****Endocrinology Institute I.C. Parhon, Bucharest, Romania
Aim: We report a rare case of Wegener granulomatosis eventually ending in catastrophic antiphospholipid syndrome.Method: A 42 year- old female patient, diagnosed and treated for Wegener granulomatosis since 14 y.o., suddenly manifests a left orbital pseudotumor. The clinical exam revealed: left orbital panniculitis, visual acuity loss, papillary oedema in the left eye and limited motility of the left globe. Results: The investigations demonstrated the presence of the infectious Lysteria monocitogenes causing orbital pseudotumor . The treatment targeted both the infectious cause and the Wegener granulomatosis. The outcome was the anatomic recovery of the left globe, but the function was lost. Discussion: Besides the granulomatosis vasculitis, the presence of the microorganisms also induces increased antiphospholipid antibodies (APLA). APLA induce cell humoral immunity disorders, as a consequence of the infectious process. Conclusion: The infection represents the mutual trigger both for the increase of cANCA and for the exacerbation of the thrombosis mechanism due to APLA, leading finally to a catastrophic antiphospholipid syndrome.The evolution pattern of the antiphospholipid antibodies leads to the catastrophic systemic inflammatory syndrome, due to the second infection impossible to controle two years after.
January 2006Patient M.F., 42 y.o., with: Left orbital panniculitis VA decreased in OS PAPILLARY STASIS OS Motility affected in OS
DIPLOPIA
History:
1992: Operated nasal septum deviation, subcutaneous nodules, partial nasal septum lesion, haemorrhagic lesions strictly around nasal septum. Maxillary sinus puncture – bacteriologic exam: pyocyaneus
DIAGNOSIS: Granulomatosis Wegener1993: biopsy + pulmonary exam cyclophosphamide 200mg
1994: one hospitalization cyclophosphamide 150 mg
1995: one hospitalization cyclophosphamide 100mg
1997 +1998: cyclophosphamide 50mg
1997-2001: Control in the Infectious diseases department
2001-2004: without cyclophosphamide – cutaneous and sinus lesions
2005 : PAS 12tb, biseptolum on her own account for necrotic cutaneous lesions over elbows and knees
2005: left hallux nail necrosis and Raynaud syndrome, recurrent necrotic cutaneous vesicles, splenic infarctions, HTN (max 170/110mmHg), left breast nodule 2cm without axillary ganglion, APS? Poze picior
2006: aspect of left inflammatory orbital pseudotumor poze 4
2006: aspect of left inflammatory orbital pseudotumor poze 4
Invastigation:
ESR = 40 mm/1hour, fibrinogen = 519, thrombocytes = 450,000 Hb = 11,9%; The tuberculin skin test (IDR) = + 15, c-ANCA = normal, C-reactive protein = normal
Lungs: pulmonary x-ray – enlarged right hilar
Kidneys : AP max = 170mmHg, creatinine = normal
Left breast nodule 2cm without axillary ganglion, normal left breast mammography,
Recurrent necrotic cutaneous vesicles
LA = positive, aß2GPI = 36UE, Protein C = 85% (N > 75%) Protein S = 62% (N > 65%), AT III = 118% (N > 80%)
ELISA for listeria IgM = 1,305 (N =0,500)
PARACLINICAL : MRI
Difuse infiltrative- edematous modific. (granulation tissue?) at the level of the left periorbitary soft tissue and wall, infiltrating extrinsic ocular muscles, lacrimal gland and partly retroorbitary fat tissue.
Left ethmoidal and frontosphenoidal sinusitis.
ENT Consultation – Prof. Dr. C. Sarafoleanu
Left anteroposterior ethmoidotomy to achieve left orbital decompression hoping to save visual function in OS.
Anatomo-pathological examination: confirms the specific aspect of Wegener Granulomatosis.
The 4th day after decompression surgery The 8th day after decompression surgery
Stage diagnosis: CLINICALLeft inflammatory orbital pseudotumor afecting all orbitary elements: - optic nerve, - oculomotory muscles, - cellulitis, - pannicullitis - vessels → hyperviscosy syndrome by rheological mechanism and affectation of vascular endothelium PARACLINICAL-biological - MRI - anatomopathological exam
Wegener disease with pluriorganic implication + ANTIPHOSPHOLIPID SYNDROME .
Clinical: Overweight Orbital and ocular affectation progressive loss of visual acuity Intermittent caudication (has
been present for 1 year) Cephaleea Cutaneous vasculitis Digital thrombosis (hallux) HTA HBP
Biological : Inflammatory syndrome pANCA 4,5 ui/ml Hb = 8,7g/dl C3 = 0,5 mg/l LA +++ Antibodies anti-β2GPI 34
EU/ml
• Solumedrol (1,5g/3 days) in recurrent pulses with evolution to remission of cutaneous vasculitis and orbitary inflammatory process.• Cyclophosphamide• Prednisone• Vessel Due F• Acenocumarol (Sintrom)• Statine• Coversion enzymes inhibitor • Calcium channel blockers
Clinical progress under the treatment, but vision loss in OS.
September 2006
Complete thrombosis of distal abdominal aort with
normal permeability of illiac arteries (possibly through colateral) Lack of vizualization on the inferior mezenteric artery
Free ascitic in medium quantity
Evolution 2 years of positive progress- clinical evaluation every 3
months
- Breathing intercurrence followed by violent abdominal pains after 4-6 days
Hospitalized
Mesenteric infarction (terminal aortic obstruction and
inferior mesenteric artery)
CT confirmed late surgery intervention
exitus
Discussion: 1.In 1992 Wegener granulomatosis was diagnosed by under skin nodules biopsy and the pyocyaneus infection was decelated by maxillary punction.2.In 2006 Wegener is confirmed by ethmoidal biopsy, although c-ANCA is not present, but an infection is decelated again (ELISA IgM for Lysteria)3.In 2006 the presence of the antiphospholipid antibodies is decelated4.In 2008 after intercurrent infection the inferior mesenteric artery and terminal aorta thrombosis occurs resulting in catastrophic antiphospholipid syndrome and Exitus. 5. Infection is a major contributor to morbidity and mortality in WG and often mimics a disease flare or manifests as atypical features caused by treatment-related immunosuppression. Providers should have a low threshold for treating suspicious symptoms with antibiotics. (7)
Conclusion: The infection represents the mutual trigger both for the increase of cANCA and for the exacerbation of the thrombosis mechanism due to APLA, leading finally to a catastrophic antiphospholipid syndrome.The evolution pattern of the antiphospholipid antibodies leads to the catastrophic systemic inflammatory syndrome, due to the second infection impossible to controle two years after.
Could the infection be the trigger of the catastrophic evolution of the Wegener granulomatosis?!
Is there any possibility that the human body should produce antiphospholipid antibodies to protect vessels endothelium against any agressive infection ?!
In conclusion
Granulomatosis ……… pyocyaneus
Orbital inflammatory pseudotumor ………….Lysteria ……..APS
Granulomatosis………..SEPSIS………..CAPS………….DEATH
References:1.Erkan D, Cervera R, Asherson RA. Catastrophic antiphospholipid syndrome: where do we stand? Arthritis Rheum 2003;48:3320-72.Piette JC, Cervera R, Levy RA, Nasonov EL, Triplett DA, Shoenfeld Y. The catastrophic antiphospholipid syndrome-Asherson's syndrome. Ann Med Interne Paris 2003;154:195-6. Medline] 3.Asherson RA, Shoenfeld Y. The role of infection in the pathogenesis of catastrophic antiphospholipid syndrome. Molecular mimicry? J Rheumatol 2000;27:12-4. Medline]4.Shoenfeld Y, Blank M, Cervera R, Font J, Raschi E, Meroni PL. Infectious origin of the antiphospholipid syndrome. Ann Rheum Dis 2006;65:2-6. Medline]5.Cervera R, Asherson RA, Acevedo ML, et al. Antiphospholipid syndrome associated with infections: clinical and microbiological characteristics of 100 patients. Ann Rheum Dis 2004;63:1312-7. Medline] 6.Asherson RA, Espinosa G, Cervera R, et al. Disseminated intravascular coagulation in catastrophic antiphospholipid syndrome: clinical and haematological characteristics of 23 patients. Ann Rheum Dis 2005;64:943-6. Medline]7. Seo P. Wegener's granulomatosis: managing more than inflammation. Curr Opin Rheum. January 2008;20:10-16. [Medline]