Evidence map›Paper›PMID 36698866›Full record

ArticleLeukemia research reports2023

A rare case of aCML associated with CNS involvement and with aggressive clinical course.

Dorela Lame, Michelangelo Pianelli, Erika Morsia, Alberto Carturan, Gaia Goteri, Stefania Mancini, Attilio Olivieri, Antonella Poloni

Open access · goldAbstract readCase Reports
In one paragraph

Article in Leukemia research reports, 2023. 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
0.3field-weighted citation impact, top 40% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

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

8 authors at 1 institution in 1 country.

Dorela LameUniversità Politecnica delle Marche, Azienda Ospedaliera Universitaria delle Marche, Hematology Clinic, Italy.
Michelangelo PianelliUniversità Politecnica delle Marche, Azienda Ospedaliera Universitaria delle Marche, Hematology Clinic, Italy.
Erika MorsiaUniversità Politecnica delle Marche, Azienda Ospedaliera Universitaria delle Marche, Hematology Clinic, Italy.
Alberto CarturanUniversità Politecnica delle Marche, Azienda Ospedaliera Universitaria delle Marche, Hematology Clinic, Italy.
Gaia GoteriUniversità Politecnica delle Marche, Azienda Ospedaliera Universitaria delle Marche, Hematology Clinic, Italy.
Stefania ManciniUniversità Politecnica delle Marche, Azienda Ospedaliera Universitaria delle Marche, Hematology Clinic, Italy.
Attilio OlivieriUniversità Politecnica delle Marche, Azienda Ospedaliera Universitaria delle Marche, Hematology Clinic, Italy.
Antonella PoloniUniversità Politecnica delle Marche, Azienda Ospedaliera Universitaria delle Marche, Hematology Clinic, Italy.
Marche Polytechnic University · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The presence of neutrophilic leukocytosis may underlie a wide variety of diseases. Some rare causes of neutrophilia might be chronic neutrophilic leukemia (CNL) and myelodysplastic/myeloproliferative neoplasm with neutrophilia (MDS with neutrophilia). Here we report a case of a 78-year-old woman who came to our ER due to severe leukocytosis and anemia on a routine check-up. The patient was asymptomatic and the last exams available showed a mild leukopenia and thrombocytopenia. The abdominal echography showed mild splenomegaly The patient underwent bone marrow (BM) examinations. One week later, the patient presented mental deterioration. The patient underwent a cranial CT and RMN that showed multiple lesions of 11 mm in the brain parenchyma, cerebellum and encephalic trunk. Another week later, the clinical presentations worsened: she was in a comatous state and feverish 40 °C unresponsive to steroid therapy. Autopsy showed a leukemic and hemorrhage infiltration in multiple organs and in the BM a cellularity of 100% represented by myeloid elements with a slowdown maturation with blasts 5%. According to WHO 2016 this case can be reported as an aCML, an MDS/MPN overlap syndrome that is difficult to differentiate from a CNL.

Indexed as

Blast phaseLeukocytosisMDS/MPNMyelodysplastic syndromesNext generation sequencing

Identifiers

PMID36698866
PMCPMC9867965
OpenAlexW4315471350

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.