Pai syndrome (median cleft palate, cutaneous nasal polyp, and midline lipoma of the corpus callosum): A case report and literature review

In this article, we describe a patient with Pai syndrome. This infant was born with an unusual median cleft of the upper lip, a pedunculated cutaneous mass that protruded from the right nostril, double frenulum of the upper lip, and median alveolar cleft. MRI showed a midline corpus callosal lipoma....

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Veröffentlicht in:	International journal of pediatric otorhinolaryngology 2005-09, Vol.69 (9), p.1247-1252
Hauptverfasser:	Szeto, Chris, Tewfik, Ted L., Jewer, David, Rideout, Arthur
Format:	Artikel
Sprache:	eng
Schlagworte:	Brain Neoplasms - diagnosis Brain Neoplasms - etiology Cleft Lip - etiology Cleft Lip - surgery Cleft Palate - etiology Cleft Palate - surgery Corpus Callosum - pathology Humans Infant, Newborn Lipoma - diagnosis Lipoma - etiology Lipoma of corpus callosum Magnetic Resonance Imaging Male Median cleft palate Nasal polyp Nasal Polyps - etiology Nasal Polyps - surgery Pai syndrome Syndrome Tomography, X-Ray Computed
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Beschreibung
Zusammenfassung:	In this article, we describe a patient with Pai syndrome. This infant was born with an unusual median cleft of the upper lip, a pedunculated cutaneous mass that protruded from the right nostril, double frenulum of the upper lip, and median alveolar cleft. MRI showed a midline corpus callosal lipoma. Mental development was normal and chromosomal analysis revealed a normal male 46, XY karyotype.
ISSN:	0165-5876 1872-8464
DOI:	10.1016/j.ijporl.2005.01.038