Evidence map›Paper›PMID 32129057›Full record

ArticleJournal of clinical research in pediatric endocrinology2020

Primary Hyperparathyroidism Presenting as Posterior Reversible Encephalopathy Syndrome: A Report of Two Cases

Rimesh Pal, Aditya Dutta, Kanhaiya Agrawal, Nimisha Jain, Pinaki Dutta, Anil Bhansali, Arunanshu Behera, Sanjay Kumar Bhadada

Open access · goldAbstract readCase Reports
In one paragraph

Article in Journal of clinical research in pediatric endocrinology, 2020. 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
0.6field-weighted citation impact, top 34% 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
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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.

Rimesh PalPost Graduate Institute of Medical Training and Research, Clinic of Endocrinology, Chandigarh, IndiaORCID 0000-0003-4859-9393
Aditya DuttaPost Graduate Institute of Medical Training and Research, Clinic of Endocrinology, Chandigarh, IndiaORCID 0000-0001-9761-6386
Kanhaiya AgrawalPost Graduate Institute of Medical Training and Research, Clinic of Endocrinology, Chandigarh, IndiaORCID 0000-0002-5819-1546
Nimisha JainPost Graduate Institute of Medical Training and Research, Clinic of Endocrinology, Chandigarh, IndiaORCID 0000-0002-2294-4905
Pinaki DuttaPost Graduate Institute of Medical Training and Research, Clinic of Endocrinology, Chandigarh, IndiaORCID 0000-0001-5415-1611
Anil BhansaliPost Graduate Institute of Medical Training and Research, Clinic of Endocrinology, Chandigarh, IndiaORCID 0000-0003-3621-4337
Arunanshu BeheraPost Graduate Institute of Medical Training and Research, Clinic of General Surgery, Chandigarh, IndiaORCID 0000-0003-0954-0372
Sanjay Kumar BhadadaPost Graduate Institute of Medical Training and Research, Clinic of Endocrinology, Chandigarh, IndiaORCID 0000-0002-0410-8778
Post Graduate Institute of Medical Education and Research · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Posterior reversible encephalopathy syndrome (PRES) is a clinico-radiological entity characterized by subcortical vasogenic edema presenting with acute neurological symptoms. Common precipitating causes include renal failure, pre-eclampsia/eclampsia, post-organ transplant, and cytotoxic drugs. Hypercalcemia is a rare cause of PRES; most cases occur in the setting of severe hypercalcemia secondary to malignancy or iatrogenic vitamin D/calcium overdose. Primary hyperparathyroidism (PHPT), as a cause of PRES, is an oddity. We report two cases of adolescent PHPT presenting with generalized tonic-clonic seizures and altered sensorium. On evaluation, both had hypertension, severe hypercalcemia (serum calcium 14.1 mg/dL and 14.5 mg/dL, respectively) and elevated parathyroid hormone levels. Magnetic resonance imaging (MRI) revealed T2/fluid-attenuated inversion recovery hyperintensities located predominantly in the parieto-occipital regions, suggestive of PRES. Identification and excision of parathyroid adenoma led to the restoration of normocalcemia. Neurological symptoms and MRI changes improved subsequently. An extensive literature search revealed only four cases of PHPTassociated PRES; none of them being in the pediatric/adolescent age group. The predominant clinical manifestations were seizures and altered sensorium. All had severe hypercalcemia; three had hypertension at presentation, while one was normotensive. Parathyroid adenomectomy led to normalization of serum calcium and resolution of neurological symptoms and radiological changes. Thus, severe hypercalcemia, although rare in PHPT, can lead to hypercalcemic crisis precipitating acute hypertension that can result in cerebral endothelial dysfunction with the breakdown of the blood-brain barrier, culminating in PRES. We therefore recommend that serum calcium levels should be checked in all patients with PRES and that PHPT be regarded as a differential diagnosis in those with underlying hypercalcemia.

Indexed as

AdolescentChildDiagnosis, DifferentialHumansHyperparathyroidism, PrimaryMalePosterior Leukoencephalopathy SyndromePrognosisRisk FactorsHypercalcemiaposterior reversible encephalopathy syndromeprimary hyperparathyroidism

Identifiers

PMID32129057
PMCPMC7711632
OpenAlexW3010128822

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.