منابع مشابه
Congenital midline nasal masses: diagnosis and management.
Congenital midline nasal masses (CMNMs) are rare lesions most commonly caused by dermoids, hemangiomas, nasal gliomas or encephaloceles. We report a case of nasal glioma and discuss the embryologic development, evaluation, and management of such CMNMs.
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with CATCH 22 syndrome to psychotic disorders. CATCH 22 syndrome is a developmental malformation caused by hemizygous deletion of 22qll chromosome which usually presents with cardiac malformations, thymic aplasia, cleft palate, hypocalcaemia and chromosome 22 deletion (Wilson et al, 1993). Recently, a high prevalence of both schizophrenia and bipolar spectrum disorders have been found in these ...
متن کاملCongenital Midline Cervical Cleft
accessory components. By collapsing the unnecessary space and reconstructing a new tragus, we achieved an ideal distance from the new tragus to the auditory canal, which could not be attained by filling the hollow using cartilage graft. Because the shape and conditions of polyotia are very inconstant and the incidence of this anomaly is rare, it is difficult to establish a uniform surgical tech...
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Congenital midline cervical cleft is a rare anomaly that typically presents in the neonatal period as a thin suprasternal vertical band of erythematous skin with a nipple-like projection superiorly, which may exude fluid. We present the clinical and pathophysiologic features and the imaging findings of this uncommon, and rarely described entity in a newborn girl.
متن کاملCongenital Midline Cervical Cleft
On palpation, sub-mental bony spur was felt. The defect was associated with limitation of neck extension. Surgery was offered. At operation the extent of the sinus was about 4-6mm. The skin defect along with its cranial and caudal lesions was excised. The surgical wound was closed with multiple z-plasties (Fig. 2). The postoperative recovery was uneventful. Histopathology of the specimen showed...
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ژورنال
عنوان ژورنال: Baylor University Medical Center Proceedings
سال: 2017
ISSN: 0899-8280,1525-3252
DOI: 10.1080/08998280.2017.11930229