Evidence map›Paper›PMID 40438813›Full record

ArticleCureus2025

Life-Threatening Pharyngolaryngeal Hematoma in a Patient With Hemophilia A.

Kenichi Yanagihara, Yasutaka Mochizuki, Atsushi Katsube, Takuya Kamio, Masaharu Akiyama

Abstract readCase Reports
In one paragraph

Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing 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

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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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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.

Kenichi YanagiharaDepartment of Otorhinolaryngology, Jikei University School of Medicine, Tokyo, JPN.
Yasutaka MochizukiDivision of Clinical Oncology and Hematology, Department of Internal Medicine, Jikei University School of Medicine, Tokyo, JPN.
Atsushi KatsubeDivision of Clinical Oncology and Hematology, Department of Internal Medicine, Jikei University School of Medicine, Tokyo, JPN.
Takuya KamioDepartment of Pediatrics, Jikei University School of Medicine, Tokyo, JPN.
Masaharu AkiyamaDepartment of Pediatrics, Jikei University School of Medicine, Tokyo, JPN.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although airway hematomas are a rare complication of hemophilia, emergency treatment is required in these cases since airway obstruction can cause asphyxia. While the main treatment for hematomas in the airway entails replacing the coagulation factor products, in cases with a high risk of asphyxia, deciding whether or not to perform a tracheotomy can be difficult. We report the case of a patient with severe hemophilia A with rapidly worsening dyspnea due to hematomas caused by an acute upper respiratory tract infection and covering the airway at the upper part of the epiglottis and the tongue base. Laryngoscopy revealed a hematoma of the tongue base, but the hypopharynx and larynx were not visible owing to the hematoma. A CT scan also showed narrowing of the airway due to the hematoma. Given the high risk of obstruction, a tracheotomy was performed under general anesthesia. Efraloctocog alfa, a recombinant coagulation factor VIII (FVIII) product with an extended half-life, was administered to maintain trough levels of coagulation FVIII at 80% or above for eight days after tracheotomy. A repeat CT scan performed four days after the tracheotomy confirmed that the hematoma had improved. The patient was discharged 18 days after the tracheotomy with the tracheostoma closed. If patients with hemophilia complain of throat discomfort or dysphagia, the airway should be assessed via laryngoscopy. Emergency tracheotomy and treatment with a recombinant coagulation factor product by a medical team comprising emergency physicians, hematologists, and otolaryngologists is required for hemophilia patients with a high risk of airway obstruction.

Indexed as

airway obstructionhematomahemophilialaryngoscopytracheotomy

Identifiers

PMID40438813
PMCPMC12119139

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