Lymphangioma of the Oral and Maxillofacial Region: A Report of Three Cases

Haidry, Naqoosh; Shivhare, Peeyush; Vaidyanathan, Aiswarya; Mokhtar, Ejaz Ahmad; Ghimire, Aayushma Chapagain

doi:10.7759/cureus.32577

Cited by 3 publications

(3 citation statements)

References 15 publications

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“…Tratamentul chirurgical în combinație cu cel general șî cel local prin sclerozare este menționat de autorii incluși în acest studiu. [16][17][18][19][20][21][22][23][24][25].…”

Section: Rezultateunclassified

Lymphangiomas in the head and neck region in children

Railean,

Gudumac,

Lisita

et al. 2023

BulMed

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The treatment of lymphangiomas in children is a challenge because of slow but insidious growth, as well as because of infiltrative growth. In the region of the head and neck in children the problem of solving is a very difficult moment. On the one hand, the damage to the organs located in this region, on the other hand, the cosmetic problem and the growth of the child. Surgical treatment is the mainstay in the treatment of lymphangiomas in children, but the only method does not solve the problem in question. The goal. Evaluation of methods of treatment of lymphangiomas in children. Materials and methods. The study was carried out on the bibliographic basis and in particular the treatment of lymphangiomas in children in the head and neck region with pharmaceutical preparations. The ones reported in the bibliography were Sirolimus and Bleomycin. Several parameters were examined in both groups - age, sex, location of neoplasm, treatment and complications following treatment Results. More severe adverse effects were found in the group of children who received Serolim compared to those who were treated by sclerotherapy with Blaomycin. Conclusion Safety is a major concern in the treatment of vascular anomalies in children. The use of Sirolimus is indicated in cases of danger to the child’s life. Further research with randomized controlled trials is needed to establish the benefits of off-label use of sirolimus in these complex pathological processes.

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“…Tratamentul chirurgical în combinație cu cel general șî cel local prin sclerozare este menționat de autorii incluși în acest studiu. [16][17][18][19][20][21][22][23][24][25].…”

Section: Rezultateunclassified

Lymphangiomas in the head and neck region in children

Railean,

Gudumac,

Lisita

et al. 2023

BulMed

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“…Las anomalías o lesiones vasculares son defectos estructurales congénitos y localizados del sistema vascular que involucran arterias, venas o vasos linfáticos pudiendo ser clasificadas en tumores o malformaciones vasculares (Haidry et al, 2022). Los linfangiomas son tumores benignos hamartomatosos de los vasos linfáticos que surgen de secuestros linfáticos que no logran comunicarse con el sistema linfático (Neville et al, 2002;Yoganna et al, 2014) esto puede ocurrir durante el desarrollo fetal dando como resultado linfangiomas congénitos.…”

Section: Introductionunclassified

“…Los linfangiomas son tumores benignos hamartomatosos de los vasos linfáticos que surgen de secuestros linfáticos que no logran comunicarse con el sistema linfático (Neville et al, 2002;Yoganna et al, 2014) esto puede ocurrir durante el desarrollo fetal dando como resultado linfangiomas congénitos. Otro origen, pueden deberse a traumatismos, inflamación, cirugía, radioterapia y obstrucción linfática denominándose linfangiomas adquiridos (Haidry et al, 2022).…”

Section: Introductionunclassified

Linfangioma Oral en Paciente con Síndrome Koolen de Vries: Presentación de Caso y Revisión de Literatura

Stierling-D,

Ramírez-V,

Lazo-R

2024

Int. J. Odontostomat.

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RESUMEN: Los linfangiomas son tumores benignos hamartomatosos de los vasos linfáticos, originadas de un secuestro del saco linfático y agrandados por un inadecuado drenaje a la falta de comunicación con los canales linfáticos centrales o a la secreción excesiva de células de revestimiento. La incidencia de estos tumores en el sistema linfático es baja con una frecuencia de 1,2 a 2,8/1.000 en niños, sin predilección por sexo. En el territorio maxilofacial se pueden distinguir tres tipos de linfangioma: linfangioma simple, linfangioma cavernoso e higroma quístico o linfangioma quístico. Clínicamente estas lesiones se presentan como masas de tejido blando indoloras y de crecimiento lento. Su aspecto clínico depende de la extensión de la lesión. Diversos métodos de tratamiento para el linfangioma han sido reportados en la literatura, siendo la escisión quirúrgica la indicada, principalmente cuando estructuras vitales no están involucradas en la lesión. En este artículo se presenta un caso de una paciente femenina de 13 años con un aumento de volumen en el bermellón del labio superior, con antecedente de síndrome Koolen De Vries, a la cual se le realizó la exéresis de la lesión.

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Lymphangioma Circumscriptum on the Buccal Mucosa: A Case Report of a Rare Entity

Gowda Venkatesha,

Arumugam Venkatachalam Sargurunathan,

Rajaram Mohan

et al. 2024

Cureus

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Hamartomatous lymphatic channel proliferation causes lymphangiomas or microcystic lymphatic malformations (MLM). They are most commonly found in the head and neck, with oral occurrences a rarity. In this case, a 34-year-old woman presented with lymphangioma circumscriptum on the buccal mucosa, a condition that typically causes asymptomatic pebbly papules. This article focuses on the clinical features of this unique case, shedding light on the treatment modalities and histological features.

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Lymphangioma of the Oral and Maxillofacial Region: A Report of Three Cases

Cited by 3 publications

References 15 publications

Lymphangiomas in the head and neck region in children

Lymphangiomas in the head and neck region in children

Linfangioma Oral en Paciente con Síndrome Koolen de Vries: Presentación de Caso y Revisión de Literatura

Lymphangioma Circumscriptum on the Buccal Mucosa: A Case Report of a Rare Entity

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