A Case of Multiple Tongue Hamartomas with Cleft Palate: 7 Years of Follow-Up

Hamartoma is a congenital benign lesion commonly found in the lungs, kidneys, colon, and other regions, but it is seldom seen in the oral cavity. Multiple hamartoma occurrences in the tongue are particularly rare. This article describes a 7-day-old female infant with multiple tongue tumors and a cleft palate, who had difficulty feeding and subsequently underwent tumor removal under general anesthesia. Nine months later, a cleft palate repair was performed. No genetic abnormalities were detected in the genetic testing. After the tumor removal, follow-ups were conducted every year to observe any recurrence of the tumors, the morphology and function of the tongue, and any systemic abnormalities. After 7 years of follow-up, there was no recurrence of the tumors, and the morphology and function of the tongue were normal, with no systemic diseases found. It is crucial to conduct multidisciplinary consultations for children diagnosed with multiple tongue hamartomas and to monitor their overall development while addressing oral lesions.

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Publication Details

Journal
Ear Nose & Throat Journal
Published
2024-10-16
DOI
https://doi.org/10.1177/01455613241272494
Citations
1
Primary Topic
Tumors and Oncological Cases
Type
article
Field-Weighted Citation Impact
0.42
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article

A Case of Multiple Tongue Hamartomas with Cleft Palate: 7 Years of Follow-Up

Yuelin Qin, Junwei Wang, Ning Hu, Runze Zhang et al.
1 citations
Ear Nose & Throat Journal
Tumors and Oncological Cases
0.42
article

A Case of Multiple Tongue Hamartomas with Cleft Palate: 7 Years of Follow-Up

Yuelin Qin, Junwei Wang, Ning Hu, Runze Zhang, Xuecai Yang
article en
1 citations

Abstract

Hamartoma is a congenital benign lesion commonly found in the lungs, kidneys, colon, and other regions, but it is seldom seen in the oral cavity. Multiple hamartoma occurrences in the tongue are particularly rare. This article describes a 7-day-old female infant with multiple tongue tumors and a cleft palate, who had difficulty feeding and subsequently underwent tumor removal under general anesthesia. Nine months later, a cleft palate repair was performed. No genetic abnormalities were detected in the genetic testing. After the tumor removal, follow-ups were conducted every year to observe any recurrence of the tumors, the morphology and function of the tongue, and any systemic abnormalities. After 7 years of follow-up, there was no recurrence of the tumors, and the morphology and function of the tongue were normal, with no systemic diseases found. It is crucial to conduct multidisciplinary consultations for children diagnosed with multiple tongue hamartomas and to monitor their overall development while addressing oral lesions.

Ear Nose & Throat Journal
Qingdao University (CN), Affiliated Hospital of Qingdao University (CN), Qingdao Women and Children's Hospital (CN)
Good health and well-being
Openalex Percentile: Top 34%
Tumors and Oncological Cases
0.42
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