Læknablaðið : fylgirit - 01.05.1978, Qupperneq 13

Læknablaðið : fylgirit - 01.05.1978, Qupperneq 13
development of arthritis proved to be 1.2 years (the median, 2.5 months), with a range of 3 weeks to a remarkable span of 9 years. One girl had periodic fever that recurred regularly every 3 months for as long as 9 years (from age 3 to 12) before she developed polyarthritis. Initially, when only arthralgia is present, fever and rash are of the greatest diagnostic value. Most often, the' fever pattern is quotidian or double quotidian, with one or two daily peaks above 39°C (102°F), while hyperpyrexia (fever to 40.5°C or 105°F) is observed only occa- sionally. Typically, diurnal ranges are wide, sometimes as much as 5°C (9°F) so that both hyperpyrexia and subnormal temperatures occur within the same day. Fever usually responds to aspirin, but the amount needed varies from patient to patient - from 90 to 130 mg/kg daily. It proved to be 110 mg in this patient weighing almost 23 kilo- grams. Occasionally, as much as 130 mg/kg may be required (as depicted here). Each time the critical amount was reduced, by as little as 0.3 gm daily, fever promptly recurred. McMinn & Bywaters have reported similar observations. Pushing above 130 mg/kg does little more than promote salicylate intcxication. Up to 15% of patients with high fever fail to respond to aspirin; in these, corticosteroids should be tried. A characteristic rash occurs in up to 9ö/o of acute febrile patients. It consists of discrete or confluent macules or maculopapules found on the trunk, face, or extremities - including the soles and palms. The eruption is usually non- pruritic, but it may itch, sometimes intensely, in about 3% of patients. Occasionally constant, the rash is more often evanescent, appearing briefly in the late after- noon or early evening, often in conjunction with fever spikes. From day to day, individual macules tend to migrate and the degree of erythema varies. The rash is most florid when the skin has been subjected to mildtrauma, such as the pressure of underclothing (the diaper in this instance). This manifestation is known as the Koebner phenomenon, and may by diagnos- tically useful when parents report rash that is not present when the child is being examined. The typical rash may then be induced by lightly scratching or rubbing the skin. Within several minutes, blotches of macules will appear that often persist for a day or two. Generalized lymphadenopathy is frequent and may be so prominent, particularly in epithrochlear or axillary nodes, as to suggest leukemia or lymphoma. Enlarged mesenteric lymph nodes may cause abdominal pain or distention that may suggest an acute surgical abdomen. In 3 of our 20 patients, such misdiagnosis led to an incon- clusive and needless exploratory laparotomy. Like high fever, rash, and lymphadenopathy, splenomegaly occurs frequently, and was present in 15 of our 20 children. Hepatomegaly is less frequent, but when massive may be accompanied by abdominal pain and distention as well as abnormalities of liver function and nonspecific histologic changes. In addition to direct hepatic involvement, abnormalities of liver function may also result from therapy with salicylates. Cardiac involvement may have serious, if not fatal, consequences, particularly myocarditis because it may rapidly induce cardiac enlargement and heart failure. Pericarditis, which is more frequent than myocarditis, is usually a benign manifestation that tends to recur. Precordial pain or dyspnea are rarely present, and most attacks remain asymptomatic and undetected unless the child is monitored regularly for evan- escent friction rub, cardiomegaly, ECG changes, or - by the most sensitive of all indicators - typical echocardiographic abnormalities. Penumonitis or pleuritis frequently accompany carditis but may also occur independently. Iridocyclitis is rare (1 patient) while subcutaneous nodules are notably absent in this mode of onset. That prominent systemic manifestations can also occur in adults with BA has gained renewed interest as a result of 2 recent publications, one entitled "Still's disease in the adult," the other "adult onset JBA." Bywaters describes 14 adults, all women, with an illness characterized by fever, rash, polyarthritis, and a raised sedimentation rate. The 9 adults reported by Aptekar had similar manifestations except that all patients were men. In both groups, serologic tests for rheumatoid factor were uniformly negative, and the onset usually occurred during early adult years. In polyartieular onset, the large joints are most frequently involved. But the arthritis may be generalized, like adult BA, with symmetrical swelling of hand and wrist joints. In younger children, a fusiform swelling between the finger joints often replaces the more typical swelling at the joints. Scant attention has been focused on involvement of the foot. Yet, the feet are affected in almost half of all patients, often constituting the major source of disability. The metatarsophalangeal joints are usuaUy the first to become swollen and tender, and may or may not be accompanied by swelling of interphalangeal joints. Affliction of the cervical spine is frequent. The earliest X-ray changes include demineralization 11
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