There are 2 distinct forms of sarcoidosis in childhood. We describe th
e clinical picture of 6 patients with sarcoidosis of the early onset t
ype. All patients had their disease onset during the first 4 years of
life. In contrast to the black predominance reported in adult patients
, our series comprised 5 whites and one Latin-American. The triad of r
ash, arthritis, and uveitis seems to be characteristic for this form.
The symptoms in our patients were comparable to those in the literatur
e. However, a long followup (9-23 yrs) allowed us to recognize severe
complications of the disease, previously not well known, such as blind
ness (4 patients), growth retardation (3 patients), heart involvement
(2 patients), renal failure (1 patient), and even death in one patient
. Pulmonary involvement was present only in one patient late in the di
sease course. This condition may be overlooked, and is sometimes misdi
agnosed, due to its rarity and to its similarities with juvenile arthr
itis. However, the clinical characteristics of the 2 diseases are diff
erent. Early and correct diagnosis is important in light of the severe
disease prognosis, and the possible therapeutic options.