Clinical Nephrology – Case Studies, Volume 6 (2018) - Issue 1 (21 - 26)

Hypercalcemia-induced acute kidney injury in a Caucasian female due to radiographically silent systemic sarcoidosis
Ramy M. Hanna1, Marian Kaldas2, Farid Arman1, Melissa Wang2, Terrance Hammer3, Deren Sinkowitz4, Anjay Rastogi1
1 Division of Nephrology, 2 Division of Rheumatology, Department of Medicine, 3 Department of Family Medicine, and 4 Division of Pulmonary and Critical Care, Department of Medicine, David Geffen School of Medicine, University of California Los Angeles (UCLA), Los Angeles, CA, USA

   

 

DOI 10.5414/CNCS109513

Abstract

Sarcoidosis is a rare autoimmune disease resulting in formation of non-necrotizing “non-caseating” granulomas generally in the lung. The disease classically strikes African American females in their fourth and fifth decades. The resulting hypercalcemia is a result of 1-α hydroxylase overexpression in granulomas with increased 1,25-dihydroxy vitamin D levels. This phenomenon can also be observed in mycobacterial and fungal infections that produce granulomas in infected patients. Thus, chronic infectious diseases are part of differential diagnosis of granulomatous processes. We present an elderly Caucasian female who presented with hypercalcemia with serum calcium of 11 – 14 mg/dL and an elevated ionized calcium of 1.4 – 1.5 mmol/L. Initially cholecalciferol supplements were stopped, but hypercalcemia persisted for more than 2 months. 1,25-dihydroxy vitamin D levels were markedly elevated with low normal 25-hydroxy vitamin D levels, angiotensin-converting enzyme levels were also high, and chest computed tomography (CT) imaging was negative for any lymphadenopathy (including perihilar lymphadenopathy). Malignancy and infectious workups were negative for fungal and mycobacterial infections. Positron emission tomography revealed several small lymph nodes in right upper lobe of lung, and biopsy of bone marrow and lung lymph-nodes revealed non-caseating granulomata. We present an atypical case of occult sarcoidosis presenting mainly with biochemical findings without any definitive imaging findings, making diagnosis a clinical challenge.

Author Details

Authors

Departments

  • 1 Division of Nephrology,
  • 2 Division of Rheumatology, Department of Medicine,
  • 3 Department of Family Medicine, and
  • 4 Division of Pulmonary and Critical Care, Department of Medicine, David Geffen School of Medicine, University of California Los Angeles (UCLA), Los Angeles, CA, USA

Address

Ramy M. Hanna, MD, FACP, FASN, University of California Los Angeles (UCLA), David Geffen School of Medicine, Department of Medicine, Division of Nephrology, 501 Deep Valley Drive, Los Angeles, CA 90274, USA
Email: [email protected]

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Citation

Ramy M. Hanna, Marian Kaldas, Farid Arman, Melissa Wang, Terrance Hammer, Deren Sinkowitz, and Anjay Rastogi.Hypercalcemia-induced acute kidney injury in a Caucasian female due to radiographically silent systemic sarcoidosis. 2018; 6: 21-26. doi: 10.5414/CNCS109513.

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