Evidence map›Paper›PMID 30008268›Full record

ArticleJournal of medical case reports2018

Distinctive vasculopathy with systemic involvement due to levamisole long-term therapy: a case report.

Bilal Aoun, Mohammad Alali, Jad A Degheili, Sami Sanjad, Claudine Vaquin, Jean Donadieu, Tim Ulinski, Salah Termos

Open access · goldAbstract readCase Reports
In one paragraph

Article in Journal of medical case reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.9field-weighted citation impact, top 22% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Levamisole and ANCA positivity in childhood nephrotic syndrome.Pediatric nephrology (Berlin, Germany) · 2021
    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

8 authors at 5 institutions in 3 countries.

Bilal AounDivision of Pediatric Nephrology, Department of Pediatrics, American University of Beirut, Beirut, Lebanon.
Mohammad AlaliHepatobiliary and Transplant Unit, Department of Surgery, Al-Amiri Hospital, Kuwait City, Kuwait.
Jad A DegheiliDivision of Urology, Department of Surgery, American University of Beirut Medical Center, Beirut, Lebanon.
Sami SanjadDivision of Pediatric Nephrology, Department of Pediatrics, American University of Beirut, Beirut, Lebanon.
Claudine VaquinDivision of Pediatric Dermatology, Armand Trousseau Hospital, Assistance Publique - Hôpitaux de Paris (AP-HP), Paris, France.
Jean DonadieuDivision of Pediatric Hematology, Armand Trousseau hospital (APHP), Paris, France.
Tim UlinskiDivision of Pediatric Nephrology, Armand Trousseau Hospital, Assistance Publique - Hôpitaux de Paris (APHP), Paris, France.
Salah TermosHepatobiliary and Transplant Unit, Department of Surgery, Al-Amiri Hospital, Kuwait City, Kuwait. dr.termos@hotmail.com.
American University of Beirut · LBAmiri Hospital · KWAssistance Publique – Hôpitaux de Paris · FRAmerican University of Beirut Medical Center · LBSorbonne Université · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLevamisole belongs to the antihelminthic class of drugs that are sometimes administered to patients with frequently relapsing or steroid-dependent nephrotic syndrome, owing to its steroid-sparing effects. Neutropenia and skin lesions, compatible with vasculitis, have been reported as drug complications, but they are rarely associated with any systemic involvement. CASE PRESENTATION: We report a case of a 9-year-old Arab boy with steroid-dependent nephrotic syndrome who was treated with levamisole after his third relapse. The drug was initially well tolerated, but mild isolated neutropenia occurred 6 months after levamisole administration. This was followed by cutaneous vasculitis of both ears and the left cheek. The patient also developed hepatosplenomegaly and anemia. Levamisole was discontinued, and his disease remained in remission. All the systemic manifestations disappeared gradually over the course of 1 month. The patient remained in remission until 1 year after levamisole withdrawal, when clinical nephrosis recurred.

conclusionsDespite levamisole's being a useful drug for maintaining remission in steroid-dependent nephrotic syndrome, patients on long-term levamisole therapy should be monitored closely to prevent serious complications that can easily be resolved by simple drug withdrawal.

Indexed as

Adjuvants, ImmunologicCheekChildEarGlucocorticoidsHumansLevamisoleMaleNecrosisNephrotic SyndromeVasculitisAdjuvants, ImmunologicGlucocorticoidsLevamisoleCutaneous vasculitisHepatosplenomegalyLevamisoleNephrotic syndromeNeutropenia

Identifiers

PMID30008268
PMCPMC6047121
OpenAlexW2843967593

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.