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Autopsy Case of Pfeiffer Syndrome Type 2, a Phenotype of Fibroblast Growth Factor Receptor-Associated Craniosynostosis Syndromes, with Tracheal Cartilage Sleeve and Abnormal Hyperplasia of Bronchial Cartilages

Patient: Female, 4-year-old Final Diagnosis: Pfeiffer syndrome Symptoms: Craniosynostosis • tracheal cartilage sleeves Medication: — Clinical Procedure: — Specialty: Pathology • Pediatrics and Neonatology OBJECTIVE: Rare disease BACKGROUND: Pfeiffer syndrome (PS) is a fibroblast growth factor recept...

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Autores principales: Katsuragi, Shin-ya, Hirose, Etsuko, Arai, Yoshifumi, Otsuki, Yoshiro, Ohki, Shigeru, Kobayashi, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8363655/
https://www.ncbi.nlm.nih.gov/pubmed/34366428
http://dx.doi.org/10.12659/AJCR.932450
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author Katsuragi, Shin-ya
Hirose, Etsuko
Arai, Yoshifumi
Otsuki, Yoshiro
Ohki, Shigeru
Kobayashi, Hiroshi
author_facet Katsuragi, Shin-ya
Hirose, Etsuko
Arai, Yoshifumi
Otsuki, Yoshiro
Ohki, Shigeru
Kobayashi, Hiroshi
author_sort Katsuragi, Shin-ya
collection PubMed
description Patient: Female, 4-year-old Final Diagnosis: Pfeiffer syndrome Symptoms: Craniosynostosis • tracheal cartilage sleeves Medication: — Clinical Procedure: — Specialty: Pathology • Pediatrics and Neonatology OBJECTIVE: Rare disease BACKGROUND: Pfeiffer syndrome (PS) is a fibroblast growth factor receptor (FGFR)-associated craniosynostosis syndrome, characterized by abnormally broad and medially deviated thumbs and great toes. Tracheal cartilage sleeve (TCS) is associated with several FGFR-associated craniosynostosis syndromes, including PS. TCS is an airway malformation in which the tracheal cartilage rings fuse with each other to form a sleeve of cartilage. CASE REPORT: The patient was a 4-year-old girl with PS, TCS, and abnormal hyperplasia of non-fused intrapulmonary cartilages. The patient showed cranial dysplasia on prenatal ultrasonography. At birth, a cloverleaf skull in association with hydrocephalus and digital malformations was apparent. These findings were consistent with PS type 2. The diagnosis of PS type 2 was confirmed from a genetic test detecting a FGFR2 mutation (Y340C). During the clinical course, she underwent several surgeries, including ventriculoperitoneal shunts, sequential cranioplasty surgeries, and tracheotomy due to upper airway abnormalities. At 4 years old, she died of multiple organ failure following aspiration pneumonia. The autopsy revealed that the tracheal cartilages had fused with each other, resulting in a condition called TCS, in which the cartilage rings and tracheal ligaments were absent. The lungs were poorly aerated, and the dilated bronchi had thickened walls surrounded by many cartilage fragments, mainly at the hilum. These cartilages tended to overlap at both ends, did not fuse, and were greatly altered in size and shape. CONCLUSIONS: We report the results of autopsy for PS with the first histopathological findings for the lungs and other visceral organs.
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spelling pubmed-83636552021-09-02 Autopsy Case of Pfeiffer Syndrome Type 2, a Phenotype of Fibroblast Growth Factor Receptor-Associated Craniosynostosis Syndromes, with Tracheal Cartilage Sleeve and Abnormal Hyperplasia of Bronchial Cartilages Katsuragi, Shin-ya Hirose, Etsuko Arai, Yoshifumi Otsuki, Yoshiro Ohki, Shigeru Kobayashi, Hiroshi Am J Case Rep Articles Patient: Female, 4-year-old Final Diagnosis: Pfeiffer syndrome Symptoms: Craniosynostosis • tracheal cartilage sleeves Medication: — Clinical Procedure: — Specialty: Pathology • Pediatrics and Neonatology OBJECTIVE: Rare disease BACKGROUND: Pfeiffer syndrome (PS) is a fibroblast growth factor receptor (FGFR)-associated craniosynostosis syndrome, characterized by abnormally broad and medially deviated thumbs and great toes. Tracheal cartilage sleeve (TCS) is associated with several FGFR-associated craniosynostosis syndromes, including PS. TCS is an airway malformation in which the tracheal cartilage rings fuse with each other to form a sleeve of cartilage. CASE REPORT: The patient was a 4-year-old girl with PS, TCS, and abnormal hyperplasia of non-fused intrapulmonary cartilages. The patient showed cranial dysplasia on prenatal ultrasonography. At birth, a cloverleaf skull in association with hydrocephalus and digital malformations was apparent. These findings were consistent with PS type 2. The diagnosis of PS type 2 was confirmed from a genetic test detecting a FGFR2 mutation (Y340C). During the clinical course, she underwent several surgeries, including ventriculoperitoneal shunts, sequential cranioplasty surgeries, and tracheotomy due to upper airway abnormalities. At 4 years old, she died of multiple organ failure following aspiration pneumonia. The autopsy revealed that the tracheal cartilages had fused with each other, resulting in a condition called TCS, in which the cartilage rings and tracheal ligaments were absent. The lungs were poorly aerated, and the dilated bronchi had thickened walls surrounded by many cartilage fragments, mainly at the hilum. These cartilages tended to overlap at both ends, did not fuse, and were greatly altered in size and shape. CONCLUSIONS: We report the results of autopsy for PS with the first histopathological findings for the lungs and other visceral organs. International Scientific Literature, Inc. 2021-08-09 /pmc/articles/PMC8363655/ /pubmed/34366428 http://dx.doi.org/10.12659/AJCR.932450 Text en © Am J Case Rep, 2021 https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Articles
Katsuragi, Shin-ya
Hirose, Etsuko
Arai, Yoshifumi
Otsuki, Yoshiro
Ohki, Shigeru
Kobayashi, Hiroshi
Autopsy Case of Pfeiffer Syndrome Type 2, a Phenotype of Fibroblast Growth Factor Receptor-Associated Craniosynostosis Syndromes, with Tracheal Cartilage Sleeve and Abnormal Hyperplasia of Bronchial Cartilages
title Autopsy Case of Pfeiffer Syndrome Type 2, a Phenotype of Fibroblast Growth Factor Receptor-Associated Craniosynostosis Syndromes, with Tracheal Cartilage Sleeve and Abnormal Hyperplasia of Bronchial Cartilages
title_full Autopsy Case of Pfeiffer Syndrome Type 2, a Phenotype of Fibroblast Growth Factor Receptor-Associated Craniosynostosis Syndromes, with Tracheal Cartilage Sleeve and Abnormal Hyperplasia of Bronchial Cartilages
title_fullStr Autopsy Case of Pfeiffer Syndrome Type 2, a Phenotype of Fibroblast Growth Factor Receptor-Associated Craniosynostosis Syndromes, with Tracheal Cartilage Sleeve and Abnormal Hyperplasia of Bronchial Cartilages
title_full_unstemmed Autopsy Case of Pfeiffer Syndrome Type 2, a Phenotype of Fibroblast Growth Factor Receptor-Associated Craniosynostosis Syndromes, with Tracheal Cartilage Sleeve and Abnormal Hyperplasia of Bronchial Cartilages
title_short Autopsy Case of Pfeiffer Syndrome Type 2, a Phenotype of Fibroblast Growth Factor Receptor-Associated Craniosynostosis Syndromes, with Tracheal Cartilage Sleeve and Abnormal Hyperplasia of Bronchial Cartilages
title_sort autopsy case of pfeiffer syndrome type 2, a phenotype of fibroblast growth factor receptor-associated craniosynostosis syndromes, with tracheal cartilage sleeve and abnormal hyperplasia of bronchial cartilages
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8363655/
https://www.ncbi.nlm.nih.gov/pubmed/34366428
http://dx.doi.org/10.12659/AJCR.932450
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