Evidence map›Paper›PMID 27408354›Full record

ArticleIndian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion2016

Acute Lymphoblastic Leukemia in the Course of Polycythemia Vera: A Case Report and Review of Literature.

Dijiong Wu, Baodong Ye, Jianping Shen, Laijun Peng, Zhiqiang Zhong, Yuhong Zhou

Open access · bronzeAbstract readCase Reports
In one paragraph

Article in Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 39% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Expression of CD markers in JAK2Oncology reviews · 2018
    Article
  3. Acute Lymphoblastic Leukemia Transformation in Polycythemia Vera: A Rare Phenomenon.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 2016
    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.

Dijiong WuDepartment of Hematology, Zhejiang Provincial Hospital of Traditional Chinese Medicine (National Clinical Research Base of TCM), Youdian Road No. 54, Hangzhou, 310006 China.
Baodong YeDepartment of Hematology, Zhejiang Provincial Hospital of Traditional Chinese Medicine (National Clinical Research Base of TCM), Youdian Road No. 54, Hangzhou, 310006 China.
Jianping ShenDepartment of Hematology, Zhejiang Provincial Hospital of Traditional Chinese Medicine (National Clinical Research Base of TCM), Youdian Road No. 54, Hangzhou, 310006 China.
Laijun PengDepartment of Clinical Laboratory, Zhejiang Provincial Hospital of Traditional Chinese Medicine (National Clinical Research Base of TCM), Hangzhou, China.
Zhiqiang ZhongDepartment of Clinical Laboratory, Zhejiang Provincial Hospital of Traditional Chinese Medicine (National Clinical Research Base of TCM), Hangzhou, China.
Yuhong ZhouDepartment of Hematology, Zhejiang Provincial Hospital of Traditional Chinese Medicine (National Clinical Research Base of TCM), Youdian Road No. 54, Hangzhou, 310006 China.
Zhejiang Provincial Hospital of TCM · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionPolycythemia vera (PV) is one of the most common forms of myeloproliferative neoplasms. Acute myeloid leukemia secondary to PV is well reported, and the mechanism has been clarified to some extent. Only a limited number of cases have been reported about the development of acute lymphoblastic leukemia (ALL) in the course of PV, and the possible underlying mechanism has not been explored well. CASE PRESENTATION: A 75-year-old patient who developed ALL 3 years after he was diagnosed with PV. The presence of remarkable splenomegaly, typical immunophenotyping of the peripheral blood and increased expression of serum fibrosis markers indicated the existence of extramedullary hematopoiesis which may ascribe to myelofibrosis. After the treatment of dosage-modulated chemotherapy, the patient got complete remission.

conclusionThe JAK2 mutation may the underlying factor that contributes to the development of ALL, and the existence of MF may indicate the progression to post- polycythemic MF, which may be a risk factor for the accelerated transformation.

Indexed as

Acute lymphocytic leukemiaJAK2 V617F mutationPolycythemia veraPost-polycythemic MF

Identifiers

PMID27408354
PMCPMC4925529
OpenAlexW1698604203

What OpenQuestion holds

Textmetadata
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.