Evidence map›Paper›PMID 41685014›Full record

ArticleCureus2026

An Unusual Cause of Cast Nephropathy in a Patient Presenting With Hypercalcemia and Renal Failure: A Case Report.

Taif Najeebi, Shruti Prem Sudha, Fatima Al-Hashimi, Mahera Roohi, Salwa Ali

Abstract readCase Reports
In one paragraph

Article in Cureus, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Taif NajeebiDepartment of Hematology, Bahrain Oncology Center, Muharraq, BHR.
Shruti Prem SudhaDepartment of Hematology, Bahrain Oncology Center, Muharraq, BHR.
Fatima Al-HashimiDepartment of Pathology, Blood Bank and Laboratory Medicine, King Hamad University Hospital, Muharraq, BHR.
Mahera RoohiDepartment of Pathology, Blood Bank and Laboratory Medicine, King Hamad University Hospital, Muharraq, BHR.
Salwa AliDepartment of Radiology, King Hamad University Hospital, Muharraq, BHR.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sarcoidosis is a multisystem disease that is typically characterized by end-organ damage due to the formation of non-necrotizing granulomas in affected tissues. The lungs and lymph nodes are the most commonly affected organs; however, almost any organ can be involved. The diagnosis of sarcoidosis is based on a compatible clinical and radiological presentation, as well as histopathological evidence of non-necrotizing granulomas in affected organs. The diagnosis can be challenging, given the variability in clinical presentation and organ involvement, especially in cases without pulmonary symptoms. Renal involvement in sarcoidosis is complex and is usually attributed to nephrocalcinosis or damage to the tubulointerstitium of the kidney caused by granulomas. Cast nephropathy, which results from injury to the renal tubules due to the toxic effects of immunoglobulin light chains excreted in the urine, has previously been described in renal sarcoidosis and is most often reported in the context of hematological malignancies such as myeloma or lymphoma. We report the case of a patient who presented with renal dysfunction, hypercalcemia, and albumin-globulin (A/G) reversal mimicking multiple myeloma, but further investigations, including imaging and tissue biopsy, ultimately established a diagnosis of sarcoidosis. This report highlights the importance of a comprehensive diagnostic approach in such multisystem disorders.

Indexed as

cast nephropathyhypercalcemianon-oliguric renal failurepetctsarcoidosis

Identifiers

PMID41685014
PMCPMC12893024

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.