Medullary sponge kidney with IgA nephropathy: a case report and literature review

Chuchu Zeng1, Yunjie Jin2, Yanzhe Wang1

  • 1Department of Nephrology, Tongren Hospital, Shanghai Jiao Tong University School of Medicine, 1111 Xianxia Road, Shanghai, 200336, China.

BMC Nephrology
|May 3, 2024
PubMed
Abstract

Insights

This case study reports the first known instance of medullary sponge kidney (MSK) coexisting with IgA nephropathy. Treatment with corticosteroids and ARBs effectively reduced proteinuria in this rare renal condition.

Area of Science:

  • Nephrology
  • Pathology

Background:

  • Medullary sponge kidney (MSK) is a rare congenital kidney malformation.
  • Association of MSK with glomerulonephritis is uncommon.
  • IgA nephropathy is a common cause of glomerulonephritis.

Observation:

  • A 27-year-old female presented with hematuria and proteinuria.
  • Imaging confirmed medullary sponge kidney.
  • Kidney biopsy revealed IgA nephropathy.

Findings:

  • The patient was diagnosed with medullary sponge kidney and IgA nephropathy.
  • This is the first reported case of this dual diagnosis.
  • Combination therapy of corticosteroids and angiotensin receptor blockers (ARBs) significantly reduced proteinuria.

Implications:

  • Highlights the importance of considering coexisting renal pathologies.
  • Precise diagnosis based on renal biopsy is crucial for effective treatment.
  • Vigilance in differential diagnosis can improve patient outcomes in rare renal conditions.