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[Hypercalcemia revealing sarcoidosis in a child]
M Kinné1, A Filleron2, R Salet1
1Service de pédiatrie, hôpital Carémeau, CHU de Nîmes, place du Professeur-Robert-Debré, 30029 Nîmes cedex 9, France.
Summary
Pediatric sarcoidosis, a rare granulomatous disease, can present with hypercalcemia. Early diagnosis is crucial, as the classic triad is often absent in children with this condition.
Area of Science:
- Pediatric Rheumatology
- Pediatric Endocrinology
- Systemic Granulomatous Diseases
Background:
- Sarcoidosis is a rare systemic granulomatous disease, particularly in children.
- Hypercalcemia is an uncommon but significant presentation of pediatric sarcoidosis.
- The classic diagnostic triad for sarcoidosis may not always be present in pediatric cases.
Observation:
- A 14-year-old boy presented with symptoms suggestive of bone marrow and lymph node sarcoidosis, accompanied by hypercalcemia.
- Literature review included 23 pediatric cases of sarcoidosis with hypercalcemia since 1990.
- Younger children with hypercalcemia as an initial symptom were diagnosed more readily.
Findings:
- Hypercalcemia in children can be a key indicator for sarcoidosis, especially when classical signs are absent.
- Common sarcoidosis locations like lungs, skin, and lymph nodes aid in diagnosis.
- Treatment with hydration, diuretics, bisphosphonates, and corticosteroids showed positive outcomes.
Implications:
- Sarcoidosis diagnosis in children is challenging due to rarity and nonspecific symptoms, often leading to delays.
- Systematic investigation for sarcoidosis is recommended in children with unexplained hypercalcemia.
- Increased awareness can improve diagnostic timelines and patient outcomes for pediatric sarcoidosis.
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