Management of Congenital Macroglossia Due to Lymphatic Malformation in a Child with Review of Literature

Lymphangiomas are uncommon congenital hamartomas of the lymphatic system with a marked predilection for the head-and-neck region accounting for 75% of all cases. Lymphangiomas rarely affect the oral cavity. Affected sites in the oral cavity may include the tongue, palate, gingiva, lips, and alveolar...

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Main Authors: Sushma Achugatla, Surendra Singh, Sonia Thakur, Rajeev Redkar
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2025-05-01
Series:Journal of Indian Association of Pediatric Surgeons
Subjects:
Online Access:https://journals.lww.com/10.4103/jiaps.jiaps_281_24
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author Sushma Achugatla
Surendra Singh
Sonia Thakur
Rajeev Redkar
author_facet Sushma Achugatla
Surendra Singh
Sonia Thakur
Rajeev Redkar
author_sort Sushma Achugatla
collection DOAJ
description Lymphangiomas are uncommon congenital hamartomas of the lymphatic system with a marked predilection for the head-and-neck region accounting for 75% of all cases. Lymphangiomas rarely affect the oral cavity. Affected sites in the oral cavity may include the tongue, palate, gingiva, lips, and alveolar ridge of the mandible. The anterior two-thirds on the dorsal surface of the tongue is the most common site for intraoral lymphangiomas leading to macroglossia, similar to the presentation in our case. Congenital macroglossia is a rare clinical condition characterized by an enlarged tongue. This enlargement can lead to a variety of oral and facial problems, with structural deformities such as diastema, disproportionate mandibular growth, and functional disorders such as difficulty in eating and swallowing, speech impairment, or even difficulty in breathing if it is severe. Macroglossia may be attributed to multiple underlying causes. These include conditions such as idiopathic muscular hypertrophy (notably in Beckwith–Wiedemann syndrome), vascular malformations (such as angiomas and lymphangiomas), tumors, and endocrine disorders. Among these causes, lymphangiomatous macroglossia is particularly rare and is characterized by diffuse involvement. This type of macroglossia typically progresses chronically, reaching a developmental plateau at puberty without any spontaneous regression. We report a case of congenital macroglossia in an 8-year-old male due to lymphatic malformation and managed successfully.
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spelling doaj-art-339fb3ad239d4c5e9e2396c2d43dcfa32025-08-20T02:28:23ZengWolters Kluwer Medknow PublicationsJournal of Indian Association of Pediatric Surgeons0971-92611998-38912025-05-0130340340610.4103/jiaps.jiaps_281_24Management of Congenital Macroglossia Due to Lymphatic Malformation in a Child with Review of LiteratureSushma AchugatlaSurendra SinghSonia ThakurRajeev RedkarLymphangiomas are uncommon congenital hamartomas of the lymphatic system with a marked predilection for the head-and-neck region accounting for 75% of all cases. Lymphangiomas rarely affect the oral cavity. Affected sites in the oral cavity may include the tongue, palate, gingiva, lips, and alveolar ridge of the mandible. The anterior two-thirds on the dorsal surface of the tongue is the most common site for intraoral lymphangiomas leading to macroglossia, similar to the presentation in our case. Congenital macroglossia is a rare clinical condition characterized by an enlarged tongue. This enlargement can lead to a variety of oral and facial problems, with structural deformities such as diastema, disproportionate mandibular growth, and functional disorders such as difficulty in eating and swallowing, speech impairment, or even difficulty in breathing if it is severe. Macroglossia may be attributed to multiple underlying causes. These include conditions such as idiopathic muscular hypertrophy (notably in Beckwith–Wiedemann syndrome), vascular malformations (such as angiomas and lymphangiomas), tumors, and endocrine disorders. Among these causes, lymphangiomatous macroglossia is particularly rare and is characterized by diffuse involvement. This type of macroglossia typically progresses chronically, reaching a developmental plateau at puberty without any spontaneous regression. We report a case of congenital macroglossia in an 8-year-old male due to lymphatic malformation and managed successfully.https://journals.lww.com/10.4103/jiaps.jiaps_281_24anterior wedge resectioncongenital macroglossiatongue reduction surgeryvenous malformation and lymphatic malformation of tongue
spellingShingle Sushma Achugatla
Surendra Singh
Sonia Thakur
Rajeev Redkar
Management of Congenital Macroglossia Due to Lymphatic Malformation in a Child with Review of Literature
Journal of Indian Association of Pediatric Surgeons
anterior wedge resection
congenital macroglossia
tongue reduction surgery
venous malformation and lymphatic malformation of tongue
title Management of Congenital Macroglossia Due to Lymphatic Malformation in a Child with Review of Literature
title_full Management of Congenital Macroglossia Due to Lymphatic Malformation in a Child with Review of Literature
title_fullStr Management of Congenital Macroglossia Due to Lymphatic Malformation in a Child with Review of Literature
title_full_unstemmed Management of Congenital Macroglossia Due to Lymphatic Malformation in a Child with Review of Literature
title_short Management of Congenital Macroglossia Due to Lymphatic Malformation in a Child with Review of Literature
title_sort management of congenital macroglossia due to lymphatic malformation in a child with review of literature
topic anterior wedge resection
congenital macroglossia
tongue reduction surgery
venous malformation and lymphatic malformation of tongue
url https://journals.lww.com/10.4103/jiaps.jiaps_281_24
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AT soniathakur managementofcongenitalmacroglossiaduetolymphaticmalformationinachildwithreviewofliterature
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