Evidence map›Paper›PMID 37995383›Full record

ArticleRevista medica del Instituto Mexicano del Seguro Social2023

[Giant tongue leading to dysphagia in light chain amyloidosis patient].

Juan José Gómez-Piña, Dulce Mariana Quiroz, Amairani Sierra-Hernández, Sergio Alberto Mendoza-Álvarez, Olga Lidia Vera-Lastra

Open access · greenAbstract readCase ReportsEnglish Abstract
In one paragraph

Article in Revista medica del Instituto Mexicano del Seguro Social, 2023. 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
–field-weighted citation impact, top 68% 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, 0 citations in OpenAlex.

  1. Review
  2. Ulcerated Tongue Borders as a Sign of Amyloidosis in a Patient with Multiple Myeloma.International journal of hematology-oncology and stem cell research · 2025
    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

5 authors at 1 institution in 1 country.

Juan José Gómez-PiñaInstituto Mexicano del Seguro Social, Centro Médico Nacional La Raza, Hospital de Especialidades "Antonio Fraga Mouret", Servicio de Medicina Interna. Ciudad de México, México.ORCID 0000-0003-2955-6152
Dulce Mariana QuirozInstituto Mexicano del Seguro Social, Centro Médico Nacional La Raza, Hospital de Especialidades "Antonio Fraga Mouret", Servicio de Patología Clínica. Ciudad de México, México.ORCID 0000-0002-2033-4716
Amairani Sierra-HernándezInstituto Mexicano del Seguro Social, Centro Médico Nacional La Raza, Hospital de Especialidades "Antonio Fraga Mouret", Servicio de Medicina Interna. Ciudad de México, México.ORCID 0000-0002-5782-0531
Sergio Alberto Mendoza-ÁlvarezInstituto Mexicano del Seguro Social, Centro Médico Nacional La Raza, Hospital de Especialidades "Antonio Fraga Mouret", Servicio de Medicina Interna. Ciudad de México, México.ORCID 0000-0002-4980-1162
Olga Lidia Vera-LastraInstituto Mexicano del Seguro Social, Centro Médico Nacional La Raza, Hospital de Especialidades "Antonio Fraga Mouret", Servicio de Medicina Interna. Ciudad de México, México.ORCID 0000-0002-8729-9775
Centro Médico Nacional La Raza · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Macroglossia as a clinical manifestation of systemic amyloidosis is a rare condition, occurring in less than 9% of all types of amyloidosis. The aim of this report is to present the diagnostic approach of a patient with macroglossia, providing a systematic approach and considering relevant diagnostic possibilities during their evaluation. Clinical case: We present the case of a 60-year-old man who presented with a progressively enlarging giant tongue for six months, causing dysphagia and reduced oral opening. A tongue biopsy was taken, which histopathologically exhibited homogenous eosinophilic amyloid-like material. Congo red staining showed amyloid material with red dye under light microscopy and apple-green birefringence under polarized light. Bone marrow biopsy showed 30% plasma cells, allowing for a definitive diagnosis of soft tissue amyloidosis. Although it is a benign lesion, localized amyloidosis should be differentiated from systemic forms. Conclusions: The approach of patients with macroglossia is complex due to the diagnostic possibilities, from endocrinological causes, neoplastic, and even by deposit; Being an isolated sign in a patient is a challenge in its approach, because the involvement of the airway is the main complication to avoid in these patients.

Indexed as

AmyloidosisDeglutition DisordersMacroglossiaCongo RedHumansMaleMiddle AgedCongo RedAmiloidosisAmyloidosisCongo RedMacroglosiaMacroglossiaRojo Congo

Identifiers

PMID37995383
PMCPMC10727766
OpenAlexW4388982103

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.