Lymphangiomatous polyp of the palatine tonsil in children

Marta Rodríguez Anzules, Enrique Guillén Lozada, Luis Blasco Santana, Ángel Moreno Juara, Saturnino Santos Santos, Margarita Bartolomé Benito
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 CLINICAL CASE: In this paper, two different cases will be presented; one of these dates from 2018 (a 6-year-old boy) and the other one from 2021, the first younger clinical case (a 3-year-old girl) of multiple and bilateral lymphangiomatous polyps of the palatine tonsils. Both these cases were diagnosed during routine procedures at our hospital which will be explained below.
 CONCLUSIONS: The clinical suspicion is based on medical history, symptoms (dysphagia, foreign body sensation) and the oral cavity examination, but the definitive diagnosis is histopathological. The treatment consists of a tonsillectomy or a simple surgical excision. Regarding the images (CT-scan or MRI) there is controversy over whether to perform these or not. Although the clinical behavior of tonsillar lymphangiomatous polys is unknown and unclear, our reported cases did not have presence of a malignancy or growth.
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Abstract

BACKGROUND: Lymphangiomatous polyp is a very uncommon benign and congenital lesion that appears mainly in the head and neck area. The polyp arises due to a vascular and lymphatic malformation. Medical publications indicate that the number of cases in children is unknown. CLINICAL CASE: In this paper, two different cases will be presented; one of these dates from 2018 (a 6-year-old boy) and the other one from 2021, the first younger clinical case (a 3-year-old girl) of multiple and bilateral lymphangiomatous polyps of the palatine tonsils. Both these cases were diagnosed during routine procedures at our hospital which will be explained below. CONCLUSIONS: The clinical suspicion is based on medical history, symptoms (dysphagia, foreign body sensation) and the oral cavity examination, but the definitive diagnosis is histopathological. The treatment consists of a tonsillectomy or a simple surgical excision. Regarding the images (CT-scan or MRI) there is controversy over whether to perform these or not. Although the clinical behavior of tonsillar lymphangiomatous polys is unknown and unclear, our reported cases did not have presence of a malignancy or growth.
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儿童腭扁桃体淋巴管瘤性息肉
背景:淋巴管瘤性息肉是一种非常罕见的良性和先天性病变,主要出现在头颈部。息肉是由血管和淋巴管畸形引起的。医学出版物表明,儿童病例的数量尚不清楚。临床病例:本文将介绍两个不同的病例;其中一例发生在2018年(一名6岁男孩),另一例发生在2021年,这是第一例更年轻的临床病例(一名3岁女孩),患者为腭扁桃体多发和双侧淋巴管瘤性息肉。这两个病例都是在我们医院的常规程序中诊断出来的,将在下面解释。结论:临床怀疑是基于病史、症状(吞咽困难、异物感)和口腔检查,但明确的诊断是组织病理学。治疗包括扁桃体切除术或简单的手术切除。关于图像(ct扫描或MRI),是否进行这些检查存在争议。虽然扁桃体淋巴管瘤多发性的临床表现尚不清楚,但我们报告的病例没有恶性肿瘤或生长。
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