Evidence map›Paper›PMID 35125114›Full record

ArticleDiagnostic pathology2022

"MYH9 mutation and squamous cell cancer of the tongue in a young adult: a novel case report".

Takako Eva Yabe, Kylie King, Susan Russell, Laveniya Satgunaseelan, Ruta Gupta, James Chen, Bruce Ashford

Open access · goldAbstract readCase Reports
In one paragraph

Article in Diagnostic pathology, 2022. 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
0.7field-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, 8 citations in OpenAlex.

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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

7 authors at 4 institutions in 1 country.

Takako Eva YabeDepartment of Head and Neck Surgery, Wollongong Hospital, Wollongong, NSW, Australia. Takako.Yabe@health.nsw.gov.au.ORCID http://orcid.org/0000-0002-4523-8595
Kylie KingIllawarra Shoalhaven Local Health District, NSW Health Pathology South, Wollongong Hospital, Wollongong, NSW, Australia.
Susan RussellKids Cancer Centre, Sydney Children's Hospital, Sydney, NSW, Australia.
Laveniya SatgunaseelanDepartment of Tissue Pathology and Diagnostic Oncology, Royal Prince Alfred Hospital, Sydney, NSW, Australia.ORCID https://orcid.org/0000-0002-7435-0834
Ruta GuptaDepartment of Tissue Pathology and Diagnostic Oncology, Royal Prince Alfred Hospital, Sydney, NSW, Australia.ORCID https://orcid.org/0000-0003-2940-313X
James ChenDepartment of Radiation Oncology, Wollongong Hospital, Wollongong, NSW, Australia.
Bruce AshfordDepartment of Head and Neck Surgery, Wollongong Hospital, Wollongong, NSW, Australia.ORCID https://orcid.org/0000-0003-4547-6611
Wollongong Hospital · AUThe University of Sydney · AUUniversity of Wollongong · AUUNSW Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe incidence of tongue cancer in young adults is on the rise. This trend is more pronounced in females. Although the aetiology is still unclear, there is mounting evidence that genetic syndromes can play a key role in development of oral cancers in this patient group. We report the first case of oral squamous cell carcinoma (oSCC) in a young adult with an MYH9-related disorder (MYH9-RD). CASE PRESENTATION: A 19-year-old female with a germline MYH9 variant (missense variant in exon 2: c.287C > T, (p.Ser96Leu)) was referred to the head and neck surgery department for investigation of a painful, thick right tongue ulcer. She was diagnosed with Epstein syndrome, an MYH9-RD, at 12 years of age. Her main phenotypic features were profound thrombocytopenia and marked renal impairment. The tongue biopsy confirmed SCC. Preoperative positron emission tomography (PET) revealed avidity in the right tongue and ipsilateral level 2A neck lymph node. With substantial preoperative multidisciplinary input, she underwent cancer ablation and microvascular free flap reconstruction. Her pathology showed a 35 mm diameter, 14 mm thick moderately differentiated SCC with perineural and lymphovascular invasion. Two out of 38 right neck nodes were positive for metastasis with extranodal extension. None of the 34 left neck nodes was involved. She had an uneventful recovery and was discharged home on day 6 postoperative day. On day 15 postoperative day, she had catastrophic bleeding in the neck with a respiratory arrest after a forceful cough. She required an emergency tracheostomy and returned to the theatre for haemostasis. Following a short inpatient stay, she was again discharged home and underwent adjuvant therapy consisting of external beam radiotherapy of 60Gy in 30 fractions. On clinical examination and PET at 6 months after surgery, she had no evidence of disease recurrence.

conclusionsMYH9-RD can present with advanced locoregional oral cavity malignancy at an early age. The combination of profound thrombocytopenia and marked renal impairment can impact heavily on routine major head and neck cancer surgery and adjuvant treatment. This rare and challenging condition underlines the importance of early detection of cancer and multidisciplinary team input.

Indexed as

Carcinoma, Squamous CellMouth NeoplasmsTongue NeoplasmsAdultEpithelial CellsFemaleHumansMutationMyosin Heavy ChainsNeck DissectionNeoplasm Recurrence, LocalNeoplasm StagingTongueYoung AdultMYH9 protein, humanMyosin Heavy ChainsEpstein syndromeFree flapMicrovascular surgeryMYH9Neck dissectionSquamous cell carcinomaTongueYoung adult

Identifiers

PMID35125114
PMCPMC8818095
OpenAlexW4210655962

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LicenceCC BY
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Registered trials

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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.