Evidence map›Paper›PMID 24551471›Full record

ArticleCase reports in rheumatology2014

Primary systemic Al amyloidosis presenting as temporal arteritis.

Hakan Emmungil, Melike Kalfa, Burcu Başarık, Hasip Kahraman, Ferhat Tanhan, Banu Yaman, Atiye Oztürk, Zehra Erdemir, Gülşen Kandiloğlu, Vedat Inal and 1 more

Abstract read
In one paragraph

Article in Case reports in rheumatology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

11 authors.

Hakan EmmungilMersin State Hospital, Department of Internal Medicine, Division of Rheumatology, Nusratiye Hometown, Kuvayi Milliye Street No. 32, 33050, Turkey.
Melike KalfaDivision of Rheumatology, Department of Internal Medicine, Mardin State Hospital, Vali Ozan Street, Mardin, Turkey.
Burcu BaşarıkDepartment of Pulmonology, Ege University Faculty of Medicine, Ege University Hospital, Ankara Street, 35040 Izmir, Turkey.
Hasip KahramanDepartment of İnfectious Disease, Ege University Faculty of Medicine, Izmir, Turkey.
Ferhat TanhanEge University Faculty of Medicine, Ege University Hospital, Ankara Street, 35040 Izmir, Turkey.
Banu YamanDepartment of Pathology, Ege University Faculty of Medicine, Ege University Hospital, Ankara Street, 35040 Izmir, Turkey.
Atiye OztürkEge University Faculty of Medicine, Ege University Hospital, Ankara Street, 35040 Izmir, Turkey.
Zehra ErdemirEge University Faculty of Medicine, Ege University Hospital, Ankara Street, 35040 Izmir, Turkey.
Gülşen KandiloğluDepartment of Pathology, Ege University Faculty of Medicine, Ege University Hospital, Ankara Street, 35040 Izmir, Turkey.
Vedat InalDivision of Rheumatology, Department of Internal Medicine, Ege University Faculty of Medicine Ege University Hospital, Ankara Street, 35040 Izmir, Turkey.
Yasemin KabasakalDivision of Rheumatology, Department of Internal Medicine, Ege University Faculty of Medicine Ege University Hospital, Ankara Street, 35040 Izmir, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Temporal arteritis is most common vasculitis in elderly and imitated by miscellaneous disorders. Temporal artery biopsy is the gold standard test in the diagnosis of giant cell arteritis (GCA). Hereby, we describe a case of a 67-year-old man who presented initially with temporal arteritis; however, a lip biopsy then revealed AL amyloidosis. In this respect, temporal artery biopsy should be performed for definitive diagnosis of GCA particularly patients with systemic symptoms and treatment resistant.

Identifiers

PMID24551471
PMCPMC3914325

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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.