Evidence map›Paper›PMID 34754521›Full record

ArticleCase reports in oncological medicine2021

An Atypical Presentation of Sinonasal Tract Alveolar Rhabdomyosarcoma in a Young Male Patient Submitted to Multimodality Treatment.

Wilber E Bernaola-Paredes, Sergio Leonardo Favareto, Valdener Bella Filho, Eloah Pascuotte Filippetti, Walkiria Pantoja Bellotto, Henrique Rocha Mazorchi Veronese, Lucas Neves de Martins Moraes, Felipe D'Almeida Costa, Antonio Cassio Assis Pellizzon

Open access · goldAbstract readCase Reports
In one paragraph

Article in Case reports in oncological medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 39% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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

9 authors at 1 institution in 1 country.

Wilber E Bernaola-ParedesDepartment of Radiation Oncology, A.C. Camargo Cancer Center, Sao Paulo, Brazil.ORCID https://orcid.org/0000-0001-7819-3883
Sergio Leonardo FavaretoDepartment of Radiation Oncology, A.C. Camargo Cancer Center, Sao Paulo, Brazil.ORCID https://orcid.org/0000-0002-3358-7042
Valdener Bella FilhoDepartment of Radiation Oncology, A.C. Camargo Cancer Center, Sao Paulo, Brazil.ORCID https://orcid.org/0000-0003-4175-0679
Eloah Pascuotte FilippettiDepartment of Radiation Oncology, A.C. Camargo Cancer Center, Sao Paulo, Brazil.ORCID https://orcid.org/0000-0002-7481-1231
Walkiria Pantoja BellottoDepartment of Radiation Oncology, A.C. Camargo Cancer Center, Sao Paulo, Brazil.ORCID https://orcid.org/0000-0003-4950-3584
Henrique Rocha Mazorchi VeroneseDepartment of Stomatology, School of Dentistry, UNIFAMINAS, Minas Gerais, Brazil.ORCID https://orcid.org/0000-0001-6990-6730
Lucas Neves de Martins MoraesDepartment of Anatomic Pathology, A.C. Camargo Cancer Center, Sao Paulo, Brazil.ORCID https://orcid.org/0000-0002-4218-8393
Felipe D'Almeida CostaDepartment of Anatomic Pathology, A.C. Camargo Cancer Center, Sao Paulo, Brazil.ORCID https://orcid.org/0000-0001-6484-6548
Antonio Cassio Assis PellizzonDepartment of Radiation Oncology, A.C. Camargo Cancer Center, Sao Paulo, Brazil.ORCID https://orcid.org/0000-0001-7503-6751
AC Camargo Hospital · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rhabdomyosarcoma (RMS), a malignant tumor derived from the neoplastic proliferation of striated skeletal muscle cells, is the most common pediatric soft tissue sarcoma. Its treatment is mainly based on neoadjuvant chemotherapy (QT+), surgical resection, and adjuvant radiotherapy (RT+). RT+ has shown satisfactory results for locoregional control of the disease, in spite of promoting local side effects. The present case report was aimed at describing the clinical and therapeutic characteristics and the management of complications resulting from multimodal therapy in a patient with an atypical presentation of RMS in the sinonasal tract. A 20-year-old Afro-descendant man complained of an expansive tumor lesion, with left eye proptosis that reduced visual acuity and caused severe regional pain. Imaging analysis showed an extensive and infiltrative lesion in the periorbital region, sinonasal tract, left maxilla, and orbital roof. According to the histopathological analysis, the diagnosis was established corresponding to parameningeal alveolar RMS that was unresectable. Treatment was initiated with three cycles of QT+ which showed partial response and later RT+. After completing half of the RT+ sessions, the patient showed a complete response with reduction in tumor volume and improvement in pain and local conditions. Side effects such as alopecia and dermatological changes induced by radiation were observed. Moreover, painful erythematous areas were observed in the region of the hard and soft palate, uvula, and oropharynx, compatible with Grade 2 mucositis lesions. After the cytological swab test, some of them were diagnosed as herpes simplex lesions; thickening and decrease in salivary flow were also found. A local drug therapy approach was instituted, and photobiomodulation was performed to manage oral complications. RT+ was shown to be effective in locoregional control of the disease; however, the early management of its undesirable effects on the surrounding tissues was required.

Identifiers

PMID34754521
PMCPMC8572639
OpenAlexW3209643953

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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.