Evidence map›Paper›PMID 29703022›Full record

ArticleMedicine2018

Adolescent PR3-ANCA-positive hypertrophic pachymeningitis: A case report and review of the literature.

Kotaro Matsumoto, Mitsuhiro Akiyama, Nobuhiko Kajio, Kotaro Otomo, Kazuko Suzuki, Naoshi Nishina, Kento Kasuya, Naoki Oishi, Kaori Kameyama, Tsutomu Takeuchi

Open access · goldAbstract readCase Reports
In one paragraph

Article in Medicine, 2018. 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
1.6field-weighted citation impact, top 16% 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, 16 citations in OpenAlex.

  1. Article
  2. Longitudinal immune cell monitoring identified CD14Arthritis research & therapy · 2020
    Article
  3. Do we need to differentiate "true" inflammatory pseudotumor from IgG4-related disease?European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery · 2019
    Article
  4. Headache, chest pain, and multiplex cranial neuropathy.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2019
    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

10 authors at 2 institutions in 2 countries.

Kotaro MatsumotoDivision of Rheumatology, Department of Internal Medicine.
Mitsuhiro AkiyamaDivision of Rheumatology, Department of Internal Medicine.
Nobuhiko KajioDivision of Rheumatology, Department of Internal Medicine.
Kotaro OtomoDivision of Rheumatology, Department of Internal Medicine.
Kazuko SuzukiDivision of Rheumatology, Department of Internal Medicine.
Naoshi NishinaDivision of Rheumatology, Department of Internal Medicine.
Kento KasuyaDepartment of Otolaryngology, Head and Neck Surgery.
Naoki OishiDepartment of Otolaryngology, Head and Neck Surgery.
Kaori KameyamaDepartment of Diagnostic Pathology, Keio University School of Medicine, Shinjuku-ku, Tokyo, Japan.
Tsutomu TakeuchiDivision of Rheumatology, Department of Internal Medicine.
Center for Rheumatology · USKeio University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

rationaleHypertrophic pachymeningitis (HP) is an uncommon, life-threatening disease that is seen in elderly patients with antineutrophil cytoplasmic antibody (ANCA) positivity. Proteinase-3 (PR3)-ANCA-positive HP has not been reported in adolescents. Here, we report the first case of adolescent PR3-ANCA-positive HP successfully treated with immunosuppressive therapy. PATIENT CONCERNS: A 14-year-old female presented with fullness and pain in her right ear unresponsive to antibiotics. Laboratory tests showed an elevated C-reactive protein and PR3-ANCA positivity. Computed tomography and magnetic resonance imaging revealed mastoiditis in the right temporal bone. Surgical biopsy revealed severe fibrosis and prominent inflammatory-cell infiltration. She received prednisolone and methotrexate therapy, and then underwent a right mastoidectomy. Five months later, she developed headache, dysarthria, and multiple cranial nerve palsies. Further imaging revealed enhancement and thickening of the right hemispheric dura. DIAGNOSIS: PR3-ANCA-positive HP.

interventionsShe was successfully treated with steroid pulse therapy for 3 days, followed by high doses of prednisolone and intravenous cyclophosphamide. OUTCOME: The treatment resulted in significant improvement of her symptoms, laboratory data, and radiologic findings. LESSONS: PR3-ANCA-positive HP can present not only in the elderly, but also in adolescence, and prompt diagnosis and treatment with immunosuppressive therapy is vital.

Indexed as

AdolescentAntibodies, Antineutrophil CytoplasmicCyclophosphamideFemaleHumansHypertrophyImmunosuppressive AgentsMeningitisMethotrexateMyeloblastinPrednisoloneAntibodies, Antineutrophil CytoplasmicCyclophosphamideImmunosuppressive AgentsMethotrexateMyeloblastinPrednisolone

Identifiers

PMID29703022
PMCPMC5944515
OpenAlexW2806439420

What OpenQuestion holds

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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.