Conn-tissue-slides-2004-0128

Conn-tissue-slides-2004-0128 - Connective Tissue Diseases...

Info iconThis preview shows page 1. Sign up to view the full content.

View Full Document Right Arrow Icon
This is the end of the preview. Sign up to access the rest of the document.

Unformatted text preview: Connective Tissue Diseases Connective Tissue Diseases UTMB Dept. of Otolaryngology Grand Rounds January 2004 Sam J. Cunningham, MD, PhD Francis B. Quinn, Jr., MD Connective Tissue Diseases Connective Tissue Diseases Perivascular collagen deposition=Collagen Vascular Diseases Autoimmune diseases­not the primary cause Exact cause remains obscure Different diseases associated with specific autoantibodies Connective Tissue Diseases Connective Tissue Diseases Disease Autoantibody Systemic Lupus Erythematosus Anti­dsDNA, Anti­SM Rheumatoid Arthritis RF, Anti­RA33 Sjogrens Syndrome Anti­Ro(SS­A),Anti­La(SS­B) Systemic Sclerosis Anti­Scl­70, Anti­centromere Polymyositis/Dermatomyositis Anti­Jo­1 Mixed Connective Tissue Disease Anti­U1­RNP Wegener’s Granulomatosus c­ANCA Connective Tissue Diseases Connective Tissue Diseases Histopathology: Connective tissue and blood vessel inflammation and abundant fibrinoid deposits Varying tissue distribution and pattern of organ involvement Symptoms nonspecific and overlapping Difficult to diagnose Systemic Lupus Erythematosus Systemic Lupus Erythematosus General autoimmune multisystem disease prevalence 1 in 2,000 9 to 1; female to male (1 in 700) peak age 15­25 immune complex deposition photosensitive skin eruptions, serositis, pneumonitis, myocarditis, nephritis, CNS involvement Systemic Lupus Erythematosus Systemic Lupus Erythematosus specific labs ­ native(Double stranded) DNA, SM antigen lupus like reaction LE cells Systemic Lupus Erythematosus: Diagnostic Systemic Lupus Erythematosus: Diagnostic Criteria Systemic Lupus Erythematosus Systemic Lupus Erythematosus Head and Neck Manifestations Malar rash first sign in 50% Erythematous maculopapular eruption after sun exposure Oral ulceration 3­5% nasal septum perforation Acute parotid enlargement 10% Xerostomia 15% Larynx and trachea involvement uncommon ­TVC thickening and paralysis, cricoarytenoid arthritis, subglottic stenosis Systemic Lupus Erythematosus Systemic Lupus Erythematosus Systemic Lupus Erythematosus Systemic Lupus Erythematosus Discoid Lupus: Cutaneous manifestations Scar upon healing Systemic Lupus Erythematosus Systemic Lupus Erythematosus Treatment: Rheumatologist involvement Avoidance of sun Use of sunscreens NSAIDS, topical and low dose steroids, antimalarials Low dose methotrexate instead of steroids Azothioprine, cyclophosphamide, high dose steroids for serious visceral involvement Symptomatic: Salivary substitutes, Klack’s solution, postprandial rinses of 1: 1 H2O2:H2O Rheumatoid Arthritis Rheumatoid Arthritis 1% of the population Women affected 2­3 X more than men Age of onset is 40­50 Juvenile form Rheumatoid Arthritis Rheumatoid Arthritis Inflammation of the synovial tissue (lymphocytic) with synovial proliferation Symmetric involvement of peripheral joints, hands, feet and wrists Occasional systemic effects:vasculitis, visceral nodules, Sjogren syndrome, pulmonary fibrosis Anti­RA­33 autoantibodies RA associated nuclear antigen (RANA) Rheumatoid Arthritis: Diagnostic Criteria Rheumatoid Arthritis: Diagnostic Criteria 1. Morning stiffness (>1h) 2. Swelling of three or more joints 3. Swelling of hand joints (prox interphalangeal, metacarpophalyngeal, or wrist) 4. Symmetric joint swelling 5. Subcutaneous nodules 6. Serum Rheumatoid Factor 7. Radiographic evidence of erosions or periarticular osteopenia in hand or wrists Criteria 1­4 must have been present continuously for 6 weeks or longer and must be observed by a physician. A diagnosis of rheumatoid arthritis requires that 4 of the 7 criteria are fulfilled. Rheumatoid Arthritis Rheumatoid Arthritis Rheumatoid Arthritis Rheumatoid Arthritis may involve the TMJ. 55% Affected 70% with radiographic evidence of TMJ involvement Juvenile form may lead to retrognathia Rheumatoid Arthritis Rheumatoid Arthritis Head and Neck Manifestations cricoarytenoid joint most common cause of cricoarytenoid arthritis 30% patients hoarse 86% pathologic involvement exertional dyspnea, ear pain, globus hoarseness rheumatoid nodules, recurrent nerve involvement stridor local/systemic steroids poss. Tracheotomy Rheumatoid Arthritis Rheumatoid Arthritis Head and Neck Manifestations CHL ossicular chain involvement flaccid TM SNHL unexplained assoc. with rheumatoid nodules cervical spine subluxation Rheumatoid Arthritis Rheumatoid Arthritis Treatment physical therapy, daily exercise, splinting, joint protection salicylates, NSAIDS, gold salts, penicillamine, hydroxychloroquine, immunosuppressive agents Cyclosporin­A prognosis 10­15 yrs of disease 50% fully employed 10% incapacitated 10­20% remission Sjogren Syndrome Sjogren Syndrome Chronic disorder characterized by immune­ mediated destruction of exocrine glands Primary vs Secondary: Primary is diagnosis of exclusion Secondary refers to the sicca complex accompanying any of the connective tissue diseases (xerophthalmia, keratoconjuntivitis, xerostomia with/without salivary gland enlargement) Sjogren Syndrome Sjogren Syndrome 1% of the population and in 10­15% of RA patients 9:1 female:male preponderance Age of onset 40­60 years Associated with a 33­44 times increased risk of lymphoma. Sjogren Syndrome Sjogren Syndrome May affect the skin, external genitalia, GI tract, kidneys, and lungs Minor salivary gland biopsy demonstrates lymphocytic infiltration. Parotid biopsy more sensitive and specific Associated with Sjogren Syndrome A (RO­ SS­A) in 60% and Sjogren Syndrome B (LA­SS­B) in 30% Sjogren Syndrome Diagnostic Criteria Sjogren Syndrome Diagnostic Criteria 1. Dry eyes (>3mos), sensation of sand or gravel in eyes, or use of tear substitutes>3x per day 2. Dry mouth (>3mos), recurrent or persistent swollen salivary glands, or frequent drinking of liquids to aid in swallowing dry foods. 3. Schirmer­I test (<5mm in 5 min) or Rose Bengal score >4. 4. >50 mononuclear cells/4mm2 glandular tissue 5. Abnormal salivary scintigraphy or parotid sialography or unstimulated salivary flow <1.5ml in 15 min 6. Presence of anti­Ro/SS­A, anti­La/SS­b, antinuclear antibodies, or rheumatoid factor. Sjogren Syndrome Sjogren Syndrome 80% experience xerostomia Difficulty chewing, dysphagia, taste changes, fissures of tongue and lips, increased dental caries and oral candidiasis Salivary gland enlargement Sicca syndrome Sjogren Syndrome Sjogren Syndrome Sjogren Syndrome: Treatment Sjogren Syndrome: Treatment Symptomatic: saliva substitutes, artificial tears, increased oral fluid intake Avoid decongestants, antihistamines, anticholinergics, diuretics Pilocarpine, antifungals, close dental follow­up, surveillance for malignancy Scleroderma Scleroderma Also known as systemic sclerosis Sclerotic skin changes often accompanied by multisystem disease. Progressive fibrosis from increased collagen deposition in intersitium and intima of small arteries and connective tissues May be benign cutaneous involvement or aggressive systemic disease. Scleroderma Scleroderma 4­12 new cases per million per year 3­4:1 female preponderance Average age of onset between 3rd and 5th decade Scleroderma Diagnostic Criteria Scleroderma Diagnostic Criteria One major criterion: scleromatous skin changes proximal to the metacarpal­ phalangeal joints Two of three minor criteria: sclerodactyly, digital pitting scars, bi­basilar pulmonary fibrosis on CXR Scleroderma Scleroderma presentation Raynaud’s phenomenon edema fingers and hands skin thickening visceral manifestations GI tract, lung, heart, kidneys, thyroid arthralgias and muscle weakness often Scleroderma Scleroderma Laboratory Studies: Anti­Scl­70, Anti­ centromere, ESR, ANA, RF and LE cells may be present Scleroderma: Head and Neck Scleroderma: Head and Neck Manifestations Dysphagia most common initial complaint: 80% exhibit pathology in distal 2/3 of esophagus on BAS: decreased or absent peristalsis, hiatal hernia, reflux Tight, thin lips with vertical perioral furrows Trismus 2nd to tight skin, not TMJ path Xerostomia, xerophthalmia, Laryngeal involvement w hoarseness Transition zone around dental roots Considered pathognomonic by some Scleroderma Scleroderma Scleroderma Scleroderma Polymyositis and Dermatomyositis Polymyositis and Dermatomyositis Proximal muscle weakness and nonsuppurative inflammation of skeletal muscle 5 cases per million per year 2:1 female:male Age 40­60, but a pediatric variant of 5­15 year old Polymyositis/Dermatomyositis Polymyositis/Dermatomyositis Diagnosis Proximal muscle weakness Elevated serum creatinine kinase Myopathic changes on electromyography Muscle biopsy with evidence of lymphocytic inflammation Dx is definitive with all four, probable with three, and possible with two. Rash accompanies these in dermatomyositis Dermatomyositis Dermatomyositis Polymyositis: Head and Neck Polymyositis: Head and Neck Manifestations Difficulty phonating and deglutition 2nd to affected tongue musculature Nasal regurg 2nd to affected pharyngeal and palatal musculature 30% with dysphagia 2nd to involvement of upper esophagus, cricopharyngeus, pharynx, and superior constrictors Aspiration pneumonia Polymyositis and Polymyositis and Dermatomyositis:Treatment Steroids for symptomatic patients Methotrexate and immunosuppressants for non­responders Relapsing Polychondritis Relapsing Polychondritis General recurring inflammation cartilaginous structures eventual fibrosis prevalence F>M 25­45 equal racial can affect any cartilaginous structure including heart valves and large arteries Polychondritis Polychondritis General diagnostic criteria recurrent chondritis of the auricles nonerosive inflammatory polyarthritis chondritis of the nasal cartilages inflammation of ocular structures chondritis of laryngeal or tracheal cartilages, cochlear (SNHL, tinnitus) vestibular (vertigo) damage Polychondritis Polychondritis General labs ESR, leukocytosis, anemia histology loss of basophilic staining of cartilage perichondral inflammation destruction fibrotic replacement Polychondritis Polychondritis Head and Neck Manifestations auricular chondritis, nonerosive arthritis most common sudden onset erythema, pain, spares EAC feature presentation in 33% present in 90% occasional LAD resolution 5­10 days with or without Polychondritis Polychondritis serous otitis, SNHL, 49% inner ear symptoms nasal chondritis develops in 75% not necessarily coincides with auricular Polychondritis Polychondritis laryngeal involvement nonproductive cough hoarseness stridor 53% airway involvement Relapsing Polychondritis Relapsing Polychondritis Treatment salicylates, ibuprofen­symptomatic relief steroids for life threatening dapsone (anti­leprosy) reduces lysozymes Mixed Connective Tissue Disease Mixed Connective Tissue Disease Coexisting features of SLE, scleroderma, and polymyositis High titers of Anti­U1RNP 80% female, 30­60 years Head and neck: combination of manifestations of the above. Treat with steroids Vasculitides Vasculitides The vasculitides are a group of diseases characterized by non infectious necrotizing vasculitis and resultant ischemia. Polyarteritis Nodosa Polyarteritis Nodosa Prototype of vasculitis Less than 1/100000 per year Males = Females 50­60 years of age Involves small and medium arteries May result from Hep B infection (30%) GI, hepatobiliary, renal, pancreas and skeletal muscles Polyarteritis Nodosa Polyarteritis Nodosa Head and neck symptoms primarily involve the ear and include SNHL and vestibular disturbance. Proposed mechanism is thromboembolic occlusion of inner ear arteries May also see CN palsies Churg­Strauss Syndrome Churg­Strauss Syndrome Also called angiitis granulomatosis Consists of small vessel vasculitis, extra vascular granulomas, and hypereosinophilia. In patients with preexisting asthma and allergic rhinitis Hypersensitivity Vasculitis Hypersensitivity Vasculitis General collective term group of diseases inflammation of small vessels circulating and deposited immune complexes skin always involved arterioles, capillaries, venules hemorrhage or classic purpura major organ system involvement less common Hypersensitivity Vasculitis Hypersensitivity Vasculitis Head and Neck Manifestations petechiae, purpura of oral and nasal mucosa angioedema serous otitis media Treatment usually self limited especially when only skin involved systemic involvement­ more aggressive Wegener’s Granulomatosis Wegener’s Granulomatosis General necrotizing granulomas of upper airway, lower airway, kidney bilateral pneumonitis 95% chronic sinusitis 90% mucosal ulceration of nasopharynx 75% renal disease 80% hallmark pathologic lesion necrotizing granulomatous vasculitis Wegener’s Granulomatosis Wegener’s Granulomatosis antineutrophil cytoplasmic antibody (c­ANCA) sensitivity 65­90% high specificity need to confirm diagnosis often 3­4 biopsies necessary nasopharynx commonly involved good site open pulmonary biopsy occasionally needed untreated mortality of 90% at two years Wegener’s Granulomatosis Wegener’s Granulomatosis antineutrophil cytoplasmic antibody (c­ANCA) sensitivity 65­90% high specificity need to confirm diagnosis often 3­4 biopsies necessary nasopharynx commonly involved good site open pulmonary biopsy occasionally needed untreated mortality of 90% at two years Wegener’s Granulomatosis Wegener’s Granulomatosis Head and Neck Manifestations nasal symptoms crusting, epistaxis, rhinnorrhea, erosion of septal cartilage, saddle deformity, recurrent sinusitis oral cavity hyperplasia of gingiva, gingivitis Wegener’s Grnaulomatosis Wegener’s Grnaulomatosis upper airway edema, ulceration of larynx (25%) significant subglottic stenosis (8.5%) otologic serous otitis media (20­25%), CHL, suppurative otitis media, SNHL, pinna changes similar to polychondritis, facial nerve palsies Wegerner’s Granulomatosis Wegerner’s Granulomatosis Treatment meticulous dental and nasal care middle ear drainage cyclophosphamide 2 mg/kg plus prednisone 1 mg/kg remission 93% azathioprine or methotrexate alternative to cyclophosphamide Wegener’s Granulomatosis Wegener’s Granulomatosis Treatment isolated sinonasal disease low dose steroids, saline irrigation, antibiotics as needed subglottic stenosis may warrant tracheotomy Wegener’s Granulomatosis Wegener’s Granulomatosis Giant Cell Arteritis (Temporal Arteritis) Giant Cell Arteritis (Temporal Arteritis) Only extracranial vessels involved Focal granulomatous inflammation of medium and small arteries Most common vasculitis Prevalence:850/100000 Age 80+ Giant Cell Arteritis Giant Cell Arteritis Most common initial complaint: Headache­boring and constant (47%), up to 90% will develop headache ESR >50mm/hr Confirmed by temporal artery biopsy of affected side: 5­ 7cm in length. If negative, biopsy contra lateral side. False negative rate of 5­40% Tender and erythematous temporal artery 50% Tender scalp Jaw ischemia 50% Lingual ischemia 25% Giant Cell Arteritis Giant Cell Arteritis Otologic: vertigo and hearing loss Dysphagia: ascending pharyngeal involvement CN deficits, vertebrobasilar insufficiency, psychosis=intracranial disease Blindness: 1/3 untreated patients Treatment with prednisone and normalizaton of ESR Giant Cell Arteritis Giant Cell Arteritis Polymyalgia Rheumatica Polymyalgia Rheumatica Seen in 50% of patients with giant cell arteritis Muscular pain, morning stiffness of proximal muscles, elevated ESR without inflammatory joint or muscle disease Low grade fever, wt loss, malaise Low dose prednisone Behcet’s Disease Behcet’s Disease Vasculitis with triad of oral and genital ulcers and uveitis or iritis Aphthous like ulcers, covered in pale pseudomembrane Painful, on lips, gingiva, buccal mucosa, tongue, palate and oropharynx Genital ulcers similar in appearance Heal in days to weeks with scarring Behcet’s Disease Behcet’s Disease Cogan’s Disease Cogan’s Disease Rare disease of young adults Vestibuloauditory dysfunction, interstitial keratitis, and nonreactive syphilis test Follows URI Symptoms: hearing loss, vertigo, tinnitis, and aural pressure. Photophobia, lacrimation, and eye pain May resolve spontaneously Hearing loss progressive and severe w decreased or absent vestibular responses on calorics Ocular symptoms tx’s with topical steroids and atropine Hearing loss avoided if tx’s with steroids within 2 weeks of onset Kawasaki Disease Kawasaki Disease Mucocutaneous lymph node syndrome Disease of children Fever, conjuctivitis, red dry lips, erythema of oral mucosa, polymorphous truncal rash, desquamation of the fingers and toes, cervical lymphadenopathy Oral cavity erythema and cervical adenopathy are presenting symptoms Cardiac abnormalities cause 1­2% mortality rate Kawasaki Disease Kawasaki Disease ...
View Full Document

Ask a homework question - tutors are online