Evidence map›Paper›PMID 30285634›Full record

ArticleBMC infectious diseases2018

Double trouble: visceral leishmaniasis in twins after traveling to Tuscany - a case report.

Charlotte Adamczick, Alexa Dierig, Tatjana Welzel, Alexandra Schifferli, Johannes Blum, Nicole Ritz

Open access · goldAbstract readCase Reports
In one paragraph

Article in BMC infectious diseases, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. A Rare Case of Imported Cutaneous Leishmaniasis Caused byTropical medicine and infectious disease · 2023
    Article
  6. Review
  7. A case of pediatric visceral leishmaniasis-related hemophagocytic lymphohistiocytosis diagnosed by mNGS.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2020
    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 3 institutions in 2 countries.

Charlotte AdamczickGerman Association for Tropical Paediatrics and International Child Health, Frankfurt, Germany.
Alexa DierigUniversity Children's Hospital Basel, Paediatric Infectious Diseases and Vaccinology, University of Basel, Basel, Switzerland.
Tatjana WelzelUniversity Children's Hospital Basel, Department of Haematology/Oncology, University of Basel, Basel, Switzerland.
Alexandra SchifferliUniversity Children's Hospital Basel, Department of Haematology/Oncology, University of Basel, Basel, Switzerland.
Johannes BlumSwiss Public Health and Tropical Institute, University of Basel, Basel, Switzerland.
Nicole RitzUniversity Children's Hospital Basel, Paediatric Infectious Diseases and Vaccinology, University of Basel, Basel, Switzerland. nicole.ritz@unibas.ch.ORCID http://orcid.org/0000-0002-1498-1685
University of Basel · CHSwiss Tropical and Public Health Institute · CHThe University of Melbourne · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLeishmaniasis is endemic in many countries worldwide, with a prevalence of 12 million people infected, and an estimated annual incidence of 500 000 visceral leishmaniasis cases. In Europe visceral leishmaniasis is considered endemic mainly in the Mediterranean countries and cases in non-endemic European countries north of the Alps have primarily been reported in returning travellers. The incubation period is typically described between 6 weeks to 6 months. The cases presented highlight the occurrence of longer incubation periods and illustrate the individual variability for progression from infection to disease. CASE PRESENTATION: We report the cases of 18-months-old twin girls living at the German-Swiss border, who developed visceral leishmaniasis 7 and 15 months after travelling to Tuscany. They presented with fever of unknown origin and pancytopenia. Both had splenomegaly and in the first case haemophagocytic lymphohistiocytosis or leukaemia was initially included in the differential diagnosis. Diagnosis of visceral leishmaniasis was confirmed by presence of intracytoplasmic localised leishmania parasites on bone marrow aspirate and/or positive leishmania serology. Both girls responded well to treatment with liposomal amphotericin B. The mother and two older siblings remained uninfected, while the father was diagnosed to be an asymptomatic carrier.

conclusionVisceral leishmaniasis is an important differential diagnosis for fever of unknown origin and pancytopenia in young children living in countries with endemic disease and highlights the importance of obtaining a detailed travel history. Hemophagocytic lymphohistiocytosis and acute leukaemia present with similar symptoms and consequently are important differential diagnoses. Factors determining progression from infection to disease are not fully understood but younger age seems to be an important risk factor. Screening of siblings from affected individuals therefore may be warranted.

Indexed as

Amphotericin BAntiprotozoal AgentsDiagnosis, DifferentialDiseases in TwinsEndemic DiseasesFemaleFeverHumansInfantItalyLeishmaniasis, VisceralLymphohistiocytosis, HemophagocyticMalePancytopeniaSplenomegalyTravelAmphotericin BAntiprotozoal Agentsliposomal amphotericin BAsymptomatic carrierLiposomal amphotericin BSand fly

Identifiers

PMID30285634
PMCPMC6167882
OpenAlexW2895170623

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.