Salivary Gland Anlage Tumor (“Congenital Pleomorphic Adenoma”)

Dehner, Louis P.; Valbuena, Luis; Perez‐Atayde, Antonio R.; Reddick, Robert L.; Askin, Frederic B.; Rosaí, Juan

doi:10.1097/00000478-199401000-00003

Cited by 74 publications

(18 citation statements)

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“…SGAT was first described in the literature by Dehner et al [3] in 1994. Prior to this description, similar lesions had been described in the literature as early as 1980.…”

Section: Discussionmentioning

confidence: 99%

“…[1][2][3][4][5][6][7][8][9][10] Patients typically present with respiratory distress if nasal obstruction is bilateral, as neonates are obligate nasal breathers. [1][2][3][4][5][6][7][8][9][10] This pedicle may easily be torn with probing, resulting in dislodgement and possible complete and unexpected airway obstruction. [1] The tumour has a male predilection and arises from the minor salivary gland tissue on the nasopharyngeal surface of the soft palate, usually pedicled to the posterior septum or posterior nasopharyngeal wall.…”

Section: Discussionmentioning

confidence: 99%

“…[1,2,5] Patients with unilateral obstruction may present later, but most cases are seen within the first two weeks of life. [1][2][3][4][5][6][7][8][9][10] No risk of malignancy has been reported, but a high mitotic index may mimic a malignant tumour. [1][2][3][4][5][6][7][8][9][10] This pedicle may easily be torn with probing, resulting in dislodgement and possible complete and unexpected airway obstruction.…”

Section: Discussionmentioning

confidence: 99%

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Salivary gland anlage tumour – a rare cause of congenital nasal obstruction

Daniller¹,

Goedhals²,

Seedat³

2014

S Afr J CH

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Salivary gland anlage tumour, also known as congenital pleomorphic adenoma, is a rare salivary hamartoma that presents in the nasopharynx of neonates. It is important to distinguish this lesion from other causes of neonatal respiratory distress. Treatment usually involves simple excision, and recurrence is rare. No cases of malignant progression have been reported in the literature. We report an interesting case referred to our unit a day a er birth with respiratory distress.S Afr J CH 2014;8(1):31-33.

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“…SGAT was first described in the literature by Dehner et al [3] in 1994. Prior to this description, similar lesions had been described in the literature as early as 1980.…”

Section: Discussionmentioning

confidence: 99%

Section: Discussionmentioning

confidence: 99%

Section: Discussionmentioning

confidence: 99%

See 1 more Smart Citation

Salivary gland anlage tumour – a rare cause of congenital nasal obstruction

Daniller¹,

Goedhals²,

Seedat³

2014

S Afr J CH

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show abstract

“…Из них около 60 % -опухоли доброкачествен-ные [6], в их числе наиболее часто выявляемые плео-морфные аденомы (смешанные опухоли). На их до-лю приходится от 40 до 80 % всех опухолей слюнных желез [2,4,7].…”

unclassified

“…Не-редко опухоль принимает вид множественных узлов [4,5]. Высокий риск рецидивов после энуклеации добро-качественных образований послужил причиной для разработки более радикальной техники хирургиче-ского вмешательства и поиска различных способов комбинированной терапии [4,[7][8][9][10]. В данном случае радикальным хирургическим способом лечения явля-ется паротидэктомия с сохранением лицевого нерва, которая имеет и послеоперационные дефекты, и может быть причиной возникновения синдрома Люси Фрей (25 % случаев [11]).…”

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