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This disease is characterized by inflammatory destructive lesions of cartilaginous structures, principally the ears, nose, trachea, and larynx Nearly 40% of cases are associated with another disease, especially either other immunologic disorders (such as SLE, rheumatoid arthritis, or Hashimoto s thyroiditis) or cancers (such as multiple myeloma) or hematologic disorders (such as myelodysplastic syndrome) The disease, which is usually episodic, affects males and females equally The cartilage is painful, swollen, and tender during an attack and subsequently becomes atrophic, resulting in permanent deformity Biopsy of the involved cartilage shows inflammation and chondrolysis Noncartilaginous manifestations of the disease include fever, episcleritis, uveitis, deafness, aortic insufficiency, and rarely glomerulonephritis In 85% of patients, a migratory, asymmetric, and seronegative arthropathy occurs, affecting both large and small joints and the costochondral junctions Diagnosing this uncommon disease is especially difficult since the signs of cartilage inflammation (such as red ears or nasal pain) may develop and be more subtle than the fever, arthritis, rash, or other systemic manifestations Prednisone, 05 1 mg/kg/d orally, is often effective Dapsone (100 200 mg/d orally) or methotrexate (75 20 mg orally per week) may also be effective, sparing the need for long-term high-dose corticosteroid treatment Involvement of the tracheobronchial tree, leading to tracheomalacia, may lead to difficult management issues



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Dib C et al Surgical treatment of the cardiac manifestations of relapsing polychondritis: overview of 33 patients identified through literature review and the Mayo Clinic records Mayo Clin Proc 2006 Jun;81(6):772 6 [PMID: 16770977]





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JavaScript can be used to open the file and read the content of the PDF file. ... To test that the function was a success, print out the extracted data using the ...

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Hen ch-Sch nlein purpura, the most common systemic vasculitis in children, occurs in adults as well Typical features are palpable purpura, abdominal pain, arthritis, and hematuria Pathologic features include leukocytoclastic vasculitis with IgA deposition The cause is not known The purpuric skin lesions are typically located on the lower extremities but may also be seen on the hands, arms, trunk, and buttocks Joint symptoms are present in the majority of patients, the knees and ankles being most commonly involved Abdominal pain secondary to vasculitis of the intestinal tract is often associated with gastrointestinal bleeding Hematuria signals the presence of a renal lesion that is usually reversible, although it occasionally may progress to renal insufficiency Children tend to have more frequent and more serious gastrointestinal vasculitis, whereas adults more often suffer from renal disease Biopsy of the kidney reveals segmental glomerulonephritis with crescents and mesangial deposition of IgA

Most commonly occurs among persons of Asian, Turkish, or Middle Eastern background, but may affect persons of any demographic profile

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ADSL SDSL VDSL Cable modem Satellite E3/T3 OC-x Wireless ATM SONET MPLS ISDN BRI ISDN PRI POTS PSTN Properties: Circuit switch Packet switch Speed Transmission media Distance 26 Categorize LAN technology types and properties Types: Ethernet 10BaseT 100BaseTX 100BaseFX 1000BaseT 1000BaseX 10GBaseSR 10GBaseLR 10GBaseER 10GBaseSW 10GBaseLW 10GBaseEW 10GBaseT

Recurrent, painful aphthous ulcers of the mouth and genitals Additional cutaneous findings include erythema nodosum like lesions, a follicular rash, and the pathergy phenomenon (formation of a sterile pustule at the site of a needle stick) Either anterior or posterior uveitis Posterior uveitis may be asymptomatic until significant damage to the retina has occurred Variety of neurologic lesions that can mimic multiple sclerosis, particularly through involvement of the white matter of the brainstem

Central nervous system involvement is another cause of major potential morbidity in Beh et s disease The central nervous system lesions that may mimic multiple sclerosis radiologically often result in serious disability or death Findings include sterile meningitis (recurrent meningeal headaches associated with a lymphocytic pleocytosis), cranial nerve palsies, seizures, encephalitis, mental disturbances, and spinal cord lesions Finally, patients with Beh et s disease have a hypercoagulable tendency that may lead to complicated venous thrombotic events, particularly multiple deep venous thrombosis, pulmonary emboli, cerebral sinus thrombosis, and other problems associated with clotting The clinical course may be chronic but is often characterized by remissions and exacerbations

Named after the Turkish dermatologist who first described it, this disease is of unknown cause Essentially all of its protean manifestations, however, are believed to result from vasculitis that may involve all types of blood vessels: small, medium, and large, on both the arterial and venous side of the circulation

5-30 Answer the following questions about the machine of Problem 5-29 (a) If E A = 430 135 V and V = 440 0 V, is this machine consuming real power from or supplying real power to the power system Is it consuming reactive power from or supplying reactive power to the power system (b) Calculate the real power P and reactive power Q supplied or consumed by the machine under the conditions in part (a) Is the machine operating within its ratings under these circumstances

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