Evidence map›Paper›PMID 31291381›Full record

ArticleBrazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica2019

Henoch-Schönlein purpura nephritis associated with monoclonal gammopathy of renal significance: a case report.

Hui Zhao, Wen-Hui Huang, Jun-Yue Huang, Shou-Yan Lu, Ya-Hong Yang, Zhi-Gang Ma

Open access · goldAbstract readCase Reports
In one paragraph

Article in Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 43% of its field
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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Article
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

6 authors at 1 institution in 1 country.

Hui ZhaoDepartment of Nephrology, Gansu Provincial Hospital, Lanzhou, Gansu, China.ORCID http://orcid.org/0000-0002-9665-314X
Wen-Hui HuangDepartment of Nephrology, Gansu Provincial Hospital, Lanzhou, Gansu, China.ORCID http://orcid.org/0000-0002-3521-6173
Jun-Yue HuangDepartment of Nephrology, Gansu Provincial Hospital, Lanzhou, Gansu, China.ORCID http://orcid.org/0000-0001-6631-4625
Shou-Yan LuDepartment of Nephrology, Gansu Provincial Hospital, Lanzhou, Gansu, China.ORCID http://orcid.org/0000-0002-4280-7959
Ya-Hong YangDepartment of Nephrology, Gansu Provincial Hospital, Lanzhou, Gansu, China.ORCID http://orcid.org/0000-0003-0091-1421
Zhi-Gang MaDepartment of Nephrology, Gansu Provincial Hospital, Lanzhou, Gansu, China.ORCID http://orcid.org/0000-0003-3577-5319
Gansu Provincial Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monoclonal gammopathy of renal significance (MGRS) can present with different morphologic features and lead to kidney failure. The Henoch-Schönlein purpura nephritis (HSPN) that cannot be relieved by treatment with glucocorticoid and immunosuppressive agents suggests the presence of monoclonal gammopathy in adult patients. The present study reports on a single case of HSPN associated with IgA-κMGRS. The patient who suffered from recurrent skin purpura for 6 months and nephrotic syndrome for 2 months was admitted to our hospital. Bone marrow biopsy showed monoclonal gammopathy of undetermined significance. Kidney biopsy indicated a Henoch-Schönlein purpura nephritis (HSPN, ISKDC classified as type III) with positive staining with κ-light chain in the glomeruli and renal tubular epithelial cells. Furthermore, skin biopsy showed leukocytoclastic vasculitis and negative staining for Congo red and light chain. Given both the renal and cutaneous involvement, the patient was considered to have HSPN associated with IgA-κMGRS. The patient experienced an exacerbation in his purpura-like lesions and clinical status after treatment with glucocorticoid and immunosuppressive agents. Consequently, the patient was put on a regimen that included dexamethasone (20 mg on the 1st, 4th, 8th, and 11th days of each month, iv) and bortezomib (2.4 mg on the 1st, 4th, 8th, and 11th days of each month, iv). Eight weeks after treatment, he had complete resolution of his cutaneous purpura and his biochemical parameters improved. The latent presence of MGRS in cases of HSPN should be considered in adult patients. Increased cognizance and correct treatment options could improve patient outcomes.

Indexed as

GlucocorticoidsHumansIgA VasculitisImmunosuppressive AgentsMaleMiddle AgedNephritisParaproteinemiasGlucocorticoidsImmunosuppressive Agents

Identifiers

PMID31291381
PMCPMC6694773
OpenAlexW2955223151

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.