Obstrucción de la vía aérea por higroma quístico en un recién nacido

Torres-Palomino, Gregory; Juárez-Domínguez, Gabriela; Guerrero‐Hernández, Manuel; Méndez-Sánchez, Lucía

doi:10.1016/j.bmhimx.2014.07.001

Cited by 4 publications

(3 citation statements)

References 12 publications

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“…According to Torres G. et al (2014). p. However, the sonographic features of fetal cystic hygroma are much more subtle in the first trimester, as first trimester hygromas differ in that the degree of cystic changes is not as well established, septations are less likely to be seen, and the early signs of its development are most likely to be recognized as a simple raised membrane-like thickening clearly separated from the posterior angles of the fetal cervixes, in light of which the first trimester hygroma can be well established by transvaginal ultrasonography According to Barrientos S. et al (2017).…”

Section: Introductionmentioning

confidence: 99%

Cystic hygroma and the importance in its prenatal diagnosis

Arévalo Suárez,

Espinosa Benítez,

Masabanda Poaquiza

et al. 2023

SIJIS

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Introduction: Cystic hygroma is a congenital malformation of the lymphatic system that presents as single cavities filled with fluid, more frequently at the cervical level and can be associated with genetic syndromes and malformations. Objective: To carry out a systematic review through the study of cystic hygroma and its importance in its prenatal diagnosis. Methodology: A qualitative systematic review of the studies focused on cystic hygroma was carried out. Literature search techniques included search engines such as Medline (Pubmed), Scielo, Elseiver. A total of 20 items are included. Results: Cystic hygromas are endothelial cell-covered cysts that arise from lymphatic malformations. Many of them affect the cervical lymph nodes and occur in the neck region. Other preferred locations are the axilla, mediastinum, groin, and retroperitoneal area, where these cystic lesions are present at birth. Conclusions: The importance of prenatal diagnosis methods are fundamental to know the potential problems that the R.N. after his birth.

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Section: Introductionmentioning

confidence: 99%

Cystic hygroma and the importance in its prenatal diagnosis

Arévalo Suárez,

Espinosa Benítez,

Masabanda Poaquiza

et al. 2023

SIJIS

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“…The mass may be small and go unnoticed at birth. However, most lesions are recognized early due to their size and associated symptoms of respiratory obstruction (dyspnea when compressing the trachea) [18,19] and problems with feeding (dysphagia when compressing the esophagus), which are the second and third most common presenting symptom.…”

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confidence: 99%

Lymphangioma: A Rare Cause of Cervical Tumor in Adults

García¹,

Rico²

2023

Preprint

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Neck lymphangiomas are rare, benign congenital malformations that predominate in childhood. Most present before the age of two. There are no risk factors related to sex, ethnic origin or predominance on either side, and they can occur in any anatomical location, although the most frequent is in the head and neck. The clinical presentation depends on its location. The most frequent symptom is the existence of a painless mass that grows slowly. Available therapeutic tools include surgery, systemic treatment, and injection of sclerosing agents.

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“…El tratamiento actualmente, se determina según el sitio de la lesión, si es de flujo linfático bajo o alto, el tamaño y los órganos comprometidos. Las alternativas terapéuticas incluyen el manejo del parto con la técnica EXIT (ex utero intrapartum treatment) para comprobar y asegurar una vía aérea permeable al minuto de nacer, el uso de láser, drenaje, cirugía, aspiración y escleroterapia 5 .…”

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Higroma quístico fetal

2020

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El higroma quístico congénito o linfangioma es un tumor del sistema linfático, es de origen embrionario y se origina por la obstrucción del drenaje de los sacos linfáticos. Su localización en orden de frecuencia es en las regiones cervical, axilar, intraperitoneal e inguinal, y muy raro como alteración única en el mediastino anterior. Paciente de 32 años de edad, con embarazo 16 sem ± 6 días y reporte de ecografía: Embarazo de 15 sem ± 20 días, normohidramnia, higroma quístico, Ausencia de hueso nasal además de una comunicación interventricular. Paciente en sala de legrado bajo sedación profunda, se obtiene producto de sexo masculino con alteraciones faciales y aumento de volumen en región cervical. Podemos concluir que, el control prenatal es importante realizar para obtener un diagnóstico precoz con examen ecográfico seriado, estudio genético, ecocardiografía fetal y para dar tratamiento quirúrgico es necesario conformar un equipo multidisciplinario.

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Obstrucción de la vía aérea por higroma quístico en un recién nacido

Cited by 4 publications

References 12 publications

Cystic hygroma and the importance in its prenatal diagnosis

Cystic hygroma and the importance in its prenatal diagnosis

Lymphangioma: A Rare Cause of Cervical Tumor in Adults

Higroma quístico fetal

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