A Rare Presentation of Renal Sarcoidosis with Severe, Recurrent Hypercalcemia Despite Low-normal Vitamin D Levels

Renal sarcoidosis is an uncommon extrapulmonary manifestation, rarely presenting with severe hypercalcemia. We describe a diagnostically challenging case of a 56-year-old female with goblet cell adenocarcinoma of the appendix, evaluated for acute kidney injury (AKI) and hypercalcemia after abnormal labs at a routine oncology visit. Initial assessment suggested a parathyroid-independent etiology. Extensive malignancy workup, including imaging and tumor markers, failed to identify an oncologic process. Despite aggressive resuscitation and bisphosphonate therapy, recurrent hypercalcemia with AKI persisted. Low-normal 1,25-dihydroxyvitamin D, and suppressed PTH further complicated diagnosis. Definitive diagnosis was made via renal biopsy, revealing granulomatous interstitial nephritis consistent with renal sarcoidosis. Treatment with corticosteroids led to rapid improvement in calcium and renal function. This case highlights the diagnostic complexity of renal sarcoidosis, especially when presenting with hypercalcemia without systemic clues. The delayed diagnosis underscores the importance of a broad differential and interdisciplinary collaboration in evaluating unexplained hypercalcemia.

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Publication Details

Journal
JCEM Case Reports
Published
2025-10-01
DOI
https://doi.org/10.1210/jcemcr/luaf255
Primary Topic
Sarcoidosis and Beryllium Toxicity Research
Type
article
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article

A Rare Presentation of Renal Sarcoidosis with Severe, Recurrent Hypercalcemia Despite Low-normal Vitamin D Levels

R. Charles, Sudhakar Neti, Durga Yerasuri, Reshma Reguram et al.
JCEM Case Reports
Sarcoidosis and Beryllium Toxicity Research
article

A Rare Presentation of Renal Sarcoidosis with Severe, Recurrent Hypercalcemia Despite Low-normal Vitamin D Levels

R. Charles, Sudhakar Neti, Durga Yerasuri, Reshma Reguram, Carly Hubers, Kendall Conway
article en

Abstract

Renal sarcoidosis is an uncommon extrapulmonary manifestation, rarely presenting with severe hypercalcemia. We describe a diagnostically challenging case of a 56-year-old female with goblet cell adenocarcinoma of the appendix, evaluated for acute kidney injury (AKI) and hypercalcemia after abnormal labs at a routine oncology visit. Initial assessment suggested a parathyroid-independent etiology. Extensive malignancy workup, including imaging and tumor markers, failed to identify an oncologic process. Despite aggressive resuscitation and bisphosphonate therapy, recurrent hypercalcemia with AKI persisted. Low-normal 1,25-dihydroxyvitamin D, and suppressed PTH further complicated diagnosis. Definitive diagnosis was made via renal biopsy, revealing granulomatous interstitial nephritis consistent with renal sarcoidosis. Treatment with corticosteroids led to rapid improvement in calcium and renal function. This case highlights the diagnostic complexity of renal sarcoidosis, especially when presenting with hypercalcemia without systemic clues. The delayed diagnosis underscores the importance of a broad differential and interdisciplinary collaboration in evaluating unexplained hypercalcemia.

JCEM Case ReportsVol. 3(12)
Trinity Health (US), Wayne State University (US), Arkana Laboratories (US)
Openalex Percentile: Top 60%
Sarcoidosis and Beryllium Toxicity Research
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A Rare Presentation of Renal Sarcoidosis with Severe, Recurrent Hypercalcemia Despite Low-normal Vitamin D Levels — R. Charles, Sudhakar Neti, et al. · JCEM Case Reports (2025) | TGRS Research Map | TGRS