Evidence map›Paper›PMID 28059092›Full record

ArticleModern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc2017

Bone marrow morphology and disease progression in congenital thrombocytopenia: a detailed clinicopathologic and genetic study of eight cases.

Hamilton C Tsang, James B Bussel, Susan Mathew, Yen-Chun Liu, Allison A Imahiyerobo, Attilio Orazi, Julia T Geyer

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In one paragraph

Article in Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

8 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
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  8. Bone Marrow Morphology Associated With GermlinePediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society
    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

7 authors at 1 institution in 1 country.

Hamilton C TsangDepartment of Pathology and Laboratory Medicine, New York-Presbyterian Hospital Weill Cornell Medicine, New York, NY, USA.
James B BusselDepartment of Pediatrics and Medicine, New York-Presbyterian Hospital Weill Cornell Medicine, New York, NY, USA.
Susan MathewDepartment of Pathology and Laboratory Medicine, New York-Presbyterian Hospital Weill Cornell Medicine, New York, NY, USA.
Yen-Chun LiuDepartment of Pathology and Laboratory Medicine, New York-Presbyterian Hospital Weill Cornell Medicine, New York, NY, USA.
Allison A ImahiyeroboDepartment of Pediatrics and Medicine, New York-Presbyterian Hospital Weill Cornell Medicine, New York, NY, USA.
Attilio OraziDepartment of Pathology and Laboratory Medicine, New York-Presbyterian Hospital Weill Cornell Medicine, New York, NY, USA.
Julia T GeyerDepartment of Pathology and Laboratory Medicine, New York-Presbyterian Hospital Weill Cornell Medicine, New York, NY, USA.
NewYork–Presbyterian Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patients with congenital thrombocytopenia have an increased risk of developing myeloid neoplasms. In these cases, the morphologic distinction between disease at baseline and at progression is challenging. This report analyzes clinicopathologic features of congenital thrombocytopenia with long-term follow-up at one referral center. Records from the last 20 years were searched for cases of congenital thrombocytopenia with bone marrow biopsies and peripheral blood smears. The clinical, morphologic, immunophenotypic, and molecular features were analyzed. Six adult and two pediatric patients were identified (six male, two female). Age range at first biopsy was 1-47 (median, 31) years. Underlying diseases included thrombocytopenia-absent radius syndrome, congenital thrombocytopenia with radial-ulnar synostosis, MYH9-related disorder, shortened telomere syndrome, congenital thrombocytopenia with ANKRD26 mutation, and familial platelet disorder with predisposition to acute myeloid leukemia. Four patients had myelodysplastic/myeloproliferative neoplasm-like marrow changes such as hypercellularity, increased myeloid to erythroid ratio, numerous micromegakaryocytes (highlighted by CD42b), and marrow fibrosis. Two patients had marrow hypoplasia and two had unremarkable marrow morphology. Three patients-all in the myelodysplastic/myeloproliferative neoplasm-like group-developed disease progression characterized by erythroid and myeloid dysplasia, elevated bone marrow blasts, and new cytogenetic abnormalities. Unlike non-familial myeloid neoplasms, congenital thrombocytopenia patients in the myelodysplastic/myeloproliferative neoplasm-like group had a long and indolent clinical course (average age at disease progression, 47 years). In summary, three distinct morphologic types of congenital thrombocytopenia were identified: a hyperplastic myelodysplastic/myeloproliferative neoplasm-like group, a hypoplastic bone marrow failure-like group, and a group with relatively normal marrow morphology. Emergence of cytogenetic abnormalities and dysplasia in non-megakaryocyte lineages correlated with disease progression.

Indexed as

AdolescentAdultBone MarrowChildChild, PreschoolDisease ProgressionFemaleHumansInfantIntercellular Signaling Peptides and ProteinsMaleMiddle AgedMolecular Motor ProteinsMyosin Heavy ChainsNuclear ProteinsRetrospective StudiesANKRD26 protein, humanIntercellular Signaling Peptides and ProteinsMolecular Motor ProteinsMYH9 protein, humanMyosin Heavy ChainsNuclear Proteins

Identifiers

PMID28059092
OpenAlexW2568828870

What OpenQuestion holds

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Registered trials

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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.