Evidence map›Paper›PMID 27790441›Full record

ArticleJournal of clinical and diagnostic research : JCDR2016

Risk Stratification in Paragangliomas with PASS (Pheochromocytoma of the Adrenal Gland Scaled Score) and Immunohistochemical Markers.

Maithili Mandar Kulkarni, Siddhi Gaurish Sinai Khandeparkar, Sanjay D Deshmukh, R R Karekar, Vandana L Gaopande, Avinash R Joshi, Mrunal V Kesari, R R Shelke

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Journal of clinical and diagnostic research : JCDR, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04788927 (Development of a Comprehensive Predictive Model for Risk of Metastatic Disease in PPGLs Based on a Combination of Clinical, Biochemical, Genetic, and Pathoanatomical Characteristics a Retrospective National Cohort Study), which is not on this map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 10% 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.

NCT04788927 not yet recruitingnot on this mapstarted 2023, after this paper: background citation

Development of a Comprehensive Predictive Model for Risk of Metastatic Disease in PPGLs Based on a Combination of Clinical, Biochemical, Genetic, and Pathoanatomical Characteristics a Retrospective National Cohort Study

TypeobservationalSponsorRigshospitalet, DenmarkRan2023 to 2027Enrolled400ConditionsParaganglioma, Pheochromocytoma, Genetic Predisposition to Disease, Pathology
3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

  1. Pooled it
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  4. Effectiveness ofAsia Oceania journal of nuclear medicine & biology · 2024
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  9. Article
  10. Atypical variant takotsubo cardiomyopathy secondary to pheochromocytoma.Proceedings (Baylor University. Medical Center) · 2022
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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.

Maithili Mandar KulkarniAssociate Professor, Department of Pathology, Shrimati Kashibai Navale Medical College and General Hospital , Pune, Maharashtra, India .
Siddhi Gaurish Sinai KhandeparkarAssociate Professor, Department of Pathology, Shrimati Kashibai Navale Medical College and General Hospital , Pune, Maharashtra, India .
Sanjay D DeshmukhProfessor, Department of Pathology, Shrimati Kashibai Navale Medical College and General Hospital , Pune, Maharashtra, India .
R R KarekarAssociate professor, Department of Medicine, Shrimati Kashibai Navale Medical College and General Hospital , Pune, Maharashtra, India .
Vandana L GaopandeProfessor, Department of Pathology, Shrimati Kashibai Navale Medical College and General Hospital , Pune, Maharashtra, India .
Avinash R JoshiProfessor, Department of Pathology, Shrimati Kashibai Navale Medical College and General Hospital , Pune, Maharashtra, India .
Mrunal V KesariAssistant Professor, Department of Pathology, Shrimati Kashibai Navale Medical College and General Hospital , Pune, Maharashtra, India .
R R ShelkeProfessor, Department of Surgery, Shrimati Kashibai Navale Medical College and General Hospital , Pune, Maharashtra, India .
Smt. Kashibai Navale Medical College and General hospital · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionParagangliomas (PGLs) are rare tumours that arise in sympathetic and parasympathetic paraganglia and are derived from neural crest cells. Presence of metastasis is the only absolute criterion for malignancy. There is no single histo-morphological feature indicating malignant potential and multiple parameters have been proposed to prognosticate the individual case. This includes studies conducted using Pheochromocytoma of the Adrenal Gland Scaled Score (PASS) and Immunohistochemical (IHC) markers.

aimWe have studied ten cases of paraganglioma and attempted to correlate the prognosis with multiple clinicopathological variables. MATERIALS AND

methodsThis study was done in a tertiary care general hospital over a period of five years. Available clinical records and histopathology slides of all patients were reviewed. Using Pheochromocytoma of the Adrenal Gland Scaled Score (PASS), we divided the cases into two groups-tumours showing high risk behaviour (PASS≥4) and tumours showing benign behaviour (PASS<4). IHC analysis was done using synaptophysin, chromogranin, S100 and Ki67. We correlated S100 immunoreactivity and Ki67 proliferative index with PASS score. Both PASS score and IHC markers were also correlated with clinical outcome.

resultsThere were six Pheochromocytomas (PHC) and four Paragangliomas (PGL). Two paragangliomas were retroperitoneal and one each was located in ear (HNPGL) and broad ligament. PASS score was ≥4 in five cases and <4 in five cases. Out of five cases in which PASS was ≥4, three cases showed clinical evidence of malignancy and two cases were benign. All the cases in which PASS was <4 were clinically benign. S100 immunoreactivity was grade 1 in two cases, grade 2 in six cases and grade 3 in two cases. The cases in which S100 immunoreactivity was grade 1 were malignant. One case in which S100 was grade 2 was clinically malignant. Ki67 labeling index was raised (>3%) in two cases, which were malignant correlated with malignant PASS score.

conclusionWe conclude that the following clinicopathological parameters should be taken into account for risk assessment of malignant behaviour of paragangliomas- location, size, PASS score, S100 immunoreactivity and Ki67 labeling index.

Indexed as

ParagangliomaPASS score pheochromocytomaS100 immunoreactivity

Identifiers

PMID27790441
PMCPMC5071941
OpenAlexW2528045576

What OpenQuestion holds

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Registered trials

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.