Miliary tuberculosis with hypercalcaemia-induced nephrogenic diabetes insipidus in an infant
Md Tousifullah1, Anuj Rastogi2
1Paediatrics, Jaswant Rai Speciality Hospital, Meerut, Uttar Pradesh, India.
Insights
Miliary tuberculosis (TB) in infants can cause severe hypercalcemia, a rare but critical condition. Prompt recognition and a multimodal treatment approach involving corticosteroids and other therapies are vital for managing this emergency.
Area of Science:
- Pediatrics
- Infectious Diseases
- Endocrinology
Background:
- Miliary tuberculosis (TB) is a severe, rare infant manifestation.
- Hypercalcemia is infrequently reported in pediatric TB, unlike in adults.
- Hypercalcemia can lead to complications like nephrogenic diabetes insipidus.
Purpose of the Study:
- To report a case of miliary TB with hypercalcemia in an infant.
- To highlight the diagnostic challenges and management strategies for this rare condition.
- To emphasize the importance of prompt recognition and multimodal treatment.
Main Methods:
- Case report of a female infant with tubercular lymphadenitis and miliary TB.
- Clinical presentation included polyuria, polydipsia, and weight loss.
- Diagnostic workup revealed hypercalcemia, suppressed parathyroid hormone, elevated vitamin D levels, and dilute polyuria.
Main Results:
- The infant presented with symptoms of hypercalcemia despite anti-tubercular therapy (ATT).
- Initial management with hydration and ATT was insufficient.
- Multimodal treatment including corticosteroids, furosemide, and zoledronic acid led to significant clinical improvement.
Conclusions:
- Hypercalcemia in pediatric miliary TB is a rare but potentially life-threatening emergency.
- Prompt diagnosis and a comprehensive treatment strategy are essential for favorable outcomes.
- This case underscores the need for vigilance in recognizing and managing hypercalcemia in infants with TB.
Abstract:
Miliary tuberculosis (TB) is a rare but severe manifestation in infancy. Hypercalcaemia, well documented in granulomatous diseases like TB and sarcoidosis in adults, is infrequently reported in children. Nephrogenic diabetes insipidus induced by hypercalcaemia is a known complication. A female infant with right-sided neck swelling for 1 month (fine-needle aspiration showed tubercular lymphadenitis), on four-drug anti-tubercular therapy (ATT), admitted with complaints of polyuria, polydipsia and progressive weight loss over the last 2 weeks. Her father was on ATT for pulmonary TB. Investigations revealed hypercalcaemia with suppressed parathyroid hormone, elevated 25-hydroxyvitamin D3 and 1,25-dihydroxyvitamin D3, high urinary calcium-to-creatinine ratio and dilute polyuria. Despite adequate hydration and ATT, hypercalcaemia persisted, necessitating corticosteroids, furosemide and a single dose of intravenous zoledronic acid. The child improved significantly with this approach. Hypercalcaemia in paediatric TB, although rare, can be a life-threatening emergency. Prompt recognition and multimodal treatment are crucial steps in management of the condition.
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