2022, Number 1
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Rev Latin Infect Pediatr 2022; 35 (1)
Late-onset childhood sarcoidosis with multiorgan involvement. Report of two cases and review of the literature
Rodríguez HR, Carbajal RL, Rojas MCM, Uña FA, Gutiérrez MG, Barrios SE
Language: Spanish
References: 58
Page: 30-45
PDF size: 600.42 Kb.
ABSTRACT
Introduction: Sarcoidosis is a systemic disease of unknown etiology. It occurs rarely in childhood. It is characterized by fever, multiorgan involvement, especially pulmonary, cutaneous, neurological, ocular, renal, articular, lymphadenopathy, hepatomegaly and splenomegaly.
Clinical case: We report two cases of late-onset infantile sarcoidosis, whose diagnosis was confirmed by histopathological study of the kidney in case 1 and of the skin in case 2. Both patients had systemic manifestations with predominance of pulmonary alterations, uveitis and hypercalcemia, hypercalciuria. They received initial treatment with steroid and mycophenolate mofetil without adequate response.
Conclusions: It is important to consider the diagnosis of sarcoidosis in patients with diffuse lung damage, uveitis, facial palsy, erythema nodosum, hypercalcemia and elevated serum angiotensin-converting enzyme levels. The complexity of this disease and the wide range of symptoms with which it may present make an interdisciplinary approach to the patient essential to assess multiple organ involvement and the timely initiation of therapy with steroids and methotrexate, in order to prevent disease progression.
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