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A child with spider bite and glomerulonephritis: a diagnostic challenge

J M Lung1, S B Mallory

  • 1Division of Dermatology, Department of Internal Medicine, Washington University School of Medicine, St. Louis Children's Hospital, St. Louis, MO 63110, USA.

Insights

A pediatric case initially suspected as a brown recluse spider bite evolved into a diagnosis of poststreptococcal glomerulonephritis, complicated by hydronephrosis. This highlights the importance of considering varied etiologies in pediatric presentations.

Area of Science:

  • Pediatric Nephrology
  • Dermatology
  • Infectious Disease

Background:

  • A previously healthy 7-year-old boy presented with symptoms initially suggestive of a brown recluse spider bite.
  • The patient exhibited a purpuric plaque on his calf, fever, and malaise.

Observation:

  • Initial presentation included a tender, erythematous, purpuric plaque on the calf with surrounding erythema and inguinal lymphadenopathy.
  • Laboratory findings revealed an elevated white blood cell count and fibrinogen, with urinalysis showing protein and red blood cells.
  • Blood cultures yielded coagulase-negative Staphylococcus epidermidis, considered a contaminant, and the skin lesion showed signs of necrosis and peeling.

Findings:

  • Despite initial suspicion of a spider bite and treatment with antibiotics, the patient developed hematuria, prompting investigation for nephritis.
  • Elevated anti-streptolysin-O titer and low C3 levels confirmed poststreptococcal glomerulonephritis as the diagnosis.
  • Renal ultrasound revealed severe left hydronephrosis with cortical atrophy, indicating ureteropelvic junction obstruction.

Implications:

  • This case underscores the diagnostic challenge in differentiating between cutaneous emergencies like spider bites and systemic conditions in children.
  • The co-occurrence of poststreptococcal glomerulonephritis and congenital hydronephrosis highlights the need for comprehensive evaluation in pediatric patients with complex presentations.
  • Early recognition and appropriate management of both infectious and congenital urinary tract abnormalities are crucial for optimal patient outcomes.

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