learn more...C. diphtheriae is a Gram-positive bacillus. Only strains which carry the tox+ gene, are capable of toxin production. The toxin has two subunits, A and B. Subunit A is responsible for clinical toxicity. Subunit B serves only to transport the toxin component to specific receptors, present chiefly on the myocardium and in the peripheral nervous system. Humans are the only natural hosts. Clinical features Diphtheria was formerly a disease of childhood but is increasingly affecting adults in countries where childhood immunization has been interrupted as in Russia and Eastern Europe. The incubation period is 2-7 days. The manifestations may be regarded as local (due to the membrane) or systemic (due to exotoxin). The presence of a membrane, however, is not essential to the diagnosis. The illness is insidious in onset and is associated with tachycardia but only low-grade fever. If complicated by infection with other bacteria such as Strep. pyogenes, fever is high and spiking. Nasal diphtheria is characterized by the presence of a unilateral, serosanguineous nasal discharge that crusts around the external nares. Pharyngeal diphtheria is associated with the greatest toxicity and is characterized by marked tonsillar and pharyngeal inflammation and the presence of a membrane. This tough greyish yellow membrane is formed by fibrin, bacteria, epithelial cells, mononuclear cells and polymorphs, and is firmly adherent to the underlying tissue. Regional lymphadenopathy, often tender, is prominent and produces the so-called 'bull-neck'. Laryngeal diphtheria is usually a result of extension of the membrane from the pharynx. A husky voice, a brassy cough, and later dyspnoea and cyanosis due to respiratory obstruction are common features. Clinically evident myocarditis occurs, often weeks later, in patients with pharyngeal or laryngeal diphtheria. Acute circulatory failure due to myocarditis may occur in convalescent individuals around the tenth day of illness and is usually fatal. Neurological manifestations occur either early in the disease (palatal and pharyngeal wall paralysis) or several weeks after its onset (cranial nerve palsies, paraesthesiae, polyneuropathy or, rarely, encephalitis). |
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