Evidence map›Paper›PMID 39630202›Full record

ArticleFamilial cancer2024

Recurrent paraneoplastic nephrotic syndrome; insights from a Lynch syndrome patient with multiple malignancies.

Myrthe A de Jong, Marije Slingerland, Lukas J A C Hawinkels, Maartje Nielsen, Augustinus S L P Crobach, Eveline S M de Jonge-Muller, Antonius J Rabelink, Alexandra M J Langers

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In one paragraph

Article in Familial cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–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

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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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

8 authors.

Myrthe A de JongDepartment of Gastroenterology and Hepatology, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0009-0006-8018-5499
Marije SlingerlandDepartment of Medical Oncology, Leiden University Medical Center, Leiden, The Netherlands.
Lukas J A C HawinkelsDepartment of Gastroenterology and Hepatology, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0002-2274-9325
Maartje NielsenDepartment of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0002-5351-1870
Augustinus S L P CrobachDepartment of Pathology, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0002-1289-4406
Eveline S M de Jonge-MullerDepartment of Gastroenterology and Hepatology, Leiden University Medical Center, Leiden, The Netherlands.
Antonius J RabelinkDepartment of Nephrology, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0001-6780-5186
Alexandra M J LangersDepartment of Gastroenterology and Hepatology, Leiden University Medical Center, Leiden, The Netherlands. a.m.j.langers@lumc.nl.ORCID 0000-0003-1627-4324

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nephrotic syndrome is a common clinical presentation of glomerulopathy. A glomerulopathy as a paraneoplastic manifestation caused by underlying malignancy is rare. In patients with a solid tumor, membranous nephropathy is the most frequent paraneoplastic glomerulopathy. We present a case of recurrent paraneoplastic nephrotic syndrome caused by minimal change disease in a patient with Lynch syndrome. Over the years, a decrease in creatinine clearance and nephrotic-range proteinuria repeatedly functioned as a warning signal for underlying malignancies; consecutively, a colon adenocarcinoma, renal cell carcinoma and gastric adenocarcinoma were diagnosed. After treatment of the malignancies the nephrotic syndrome resolved without immunosuppressive therapy. Our patient also developed a primary lung carcinoma thrice, which did not cause an exacerbation of the minimal change disease. To further elucidate the mechanism behind the development of this phenomenon, we performed immunohistochemical analysis for vascular endothelial growth factor (VEGF) on the different tumor specimens. We found a high VEGF expression in the gastro-intestinal tumors, whereas the VEGF expression in the lung tumors was low, suggesting an association between VEGF expression and the development of paraneoplastic minimal change disease. This case report not only underlines the importance of considering a malignancy as a cause for (recurrent) nephrotic syndrome, especially in patients with an increased risk of developing malignancies like Lynch syndrome patients, but also suggests a role for VEGF in the pathogenesis of paraneoplastic minimal change disease.

Indexed as

Colorectal Neoplasms, Hereditary NonpolyposisNephrotic SyndromeParaneoplastic SyndromesAdenocarcinomaCarcinoma, Renal CellColonic NeoplasmsFemaleHumansKidney NeoplasmsLung NeoplasmsMaleMiddle AgedNeoplasms, Multiple PrimaryNephrosis, LipoidRecurrenceStomach NeoplasmsVascular Endothelial Growth Factor AVEGFA protein, humanLynch syndromeMinimal change diseaseNephrotic syndromeParaneoplasticVEGF

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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.