Evidence map›Paper›PMID 36923225›Full record

ArticleFrontiers in endocrinology2023

Case report: Metastatic pancreatic neuroendocrine tumour associated with portal vein thrombosis; successful management with subsequent pregnancies.

Lívia Sira, Noémi Zsíros, László Bidiga, Sándor Barna, Zsolt Kanyári, Edit B Nagy, Nicolas Guillaume, Damian Wild, Katalin Rázsó, Szilvia Andó and 3 more

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In one paragraph

Article in Frontiers in endocrinology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
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

13 authors at 2 institutions in 2 countries.

Lívia SiraDivision of Endocrinology, Department of Internal Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Noémi ZsírosDivision of Endocrinology, Department of Internal Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
László BidigaDepartment of Pathology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Sándor BarnaDepartment of Nuclear Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Zsolt KanyáriDepartment of Surgery, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Edit B NagyDepartment of Radiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Nicolas GuillaumeClinic of Radiology and Nuclear Medicine, University of Basel Hospital, Basel, Switzerland.
Damian WildClinic of Radiology and Nuclear Medicine, University of Basel Hospital, Basel, Switzerland.
Katalin RázsóDivision of Haematology, Department of Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Szilvia AndóDivision of Clinical Genetics, Department of Laboratory Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
István BaloghDivision of Clinical Genetics, Department of Laboratory Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Endre V NagyDivision of Endocrinology, Department of Internal Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Zoltán BaloghDivision of Endocrinology, Department of Internal Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
University of Debrecen · HUUniversity of Basel · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Splanchnic vein thrombosis due to co-existing metastatic pancreatic neuroendocrine tumour (pNET) and JAK2V617F mutation is a rare condition. Case report: Here we present a case of a young woman with complete remission of a non-functioning grade 2 pNET with unresectable liver metastases, coexisting with JAK2V617F mutation. Splenectomy and distal pancreatectomy were performed. Neither surgical removal, nor radiofrequency ablation of the liver metastases was possible. Therefore, somatostatin analogue (SSA) and enoxaparine were started. Peptide receptor radionuclide therapy (PRRT) was given in 3 cycles 6-8 weeks apart. Genetic testing revealed no multiple endocrine neoplasia type 1 (MEN-1) gene mutations. After shared decision making with the patient, she gave birth to two healthy children, currently 2 and 4 years old. On pregnancy confirmation, SSA treatment was interrupted and resumed after each delivery. Ten years after the diagnosis of pNET, no tumour is detectable by MRI or somatostatin receptor scintigraphy. PRRT followed by continuous SSA therapy, interrupted only during pregnancies, resulted in complete remission and enabled the patient to complete two successful pregnancies.

Indexed as

Adenoma, Islet CellLiver NeoplasmsNeoplasms, Second PrimaryNeuroectodermal Tumors, PrimitiveNeuroendocrine TumorsPancreatic NeoplasmsThrombosisFemaleHumansPortal VeinPregnancySomatostatinSomatostatincomplete remissionmetastatic pancreatic neuroendocrine tumourpregnancysplanchnic vein thrombosisthrombocytosis

Identifiers

PMID36923225
PMCPMC10008953
OpenAlexW4322504152

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read29
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.