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Revista de Especialidades Médico-Quirúrgicas

Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado
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2008, Number 1

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Rev Esp Med Quir 2008; 13 (1)

Nasal neuroglyal heterotopy in a newborn. A case report and bibliographic review

Astorga TR, Peñaflor AER, Castañeda GMA
Full text How to cite this article

Language: Spanish
References: 6
Page: 32-34
PDF size: 236.59 Kb.


Key words:

nasal glyoma, clinical case, Mexico.

ABSTRACT

Nasal glyomas are benign tumors which occur in one of 30,000 live newborns in the United States. They may be intranasal (30%), extranasal (60%) or a combination of both (10%). Nasal glyoma is the most frequent form of heterotopic cerebral tissue. It is seen in either sex. It is usually a single anomaly, i.e., no other associated congenital anomalies are present. A fibrous connection through the cribiform plate and the intracraneal space may be present in 15% of the cases. We report the clinical case of a 30 day old baby girl who presented with a nasal tumor which was successfully removed. The pathological diagnosis was nasal glyoma. Three months postoperatively the patient is in good condition.


REFERENCES

  1. Soham R, Anil G. Pathology quizzes case. Arch Otolaryngol Head Neck Surg 2002;28:721-2.

  2. Brown K, Rodriguez K, Brown OE. Congenital malformations of the nose. In: Cummings, Flint, Harker, Haughey, Richardson, Robbins and Schuller. Otolaryngology Head and Neck Surgery. 4a ed. Pennsylvania: Elsevier Mosby, 2005;pp:4099-5109.

  3. Jartti PH, Jartti AE, Karttunen AI, Paakko AE, et al. Magnetic resonance of a nasal glioma in a young infant: A case report. Act Radiol 2002;43:141-3.

  4. Durón Martínez J. Glioma nasal, reporte de un caso clínico. Rev Med Hond 2002;70:120-4.

  5. Hedlund G. Congenital frontonasal masses: Developmental anatomy, malformations and MR imaging. Paediatr Radiol 2006;36:647-62.

  6. Lee KJ. Otorrinolaringología y cirugía de cabeza y cuello. 7a ed. México: McGraw-Hill, 2004.




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Rev Esp Med Quir. 2008;13