1. Cholesterol granuloma in an antrochoanal polyp. A rare lesion in children.
- Author
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Val-Bernal JF, Martino M, Castaneda-Curto N, García-Triana M, and Teigeiro-Núñez V
- Subjects
- Adenoidectomy, Child, Diagnosis, Differential, Endoscopy, Female, Granuloma diagnostic imaging, Granuloma metabolism, Granuloma surgery, Humans, Maxillary Sinus diagnostic imaging, Maxillary Sinus surgery, Nasal Polyps chemistry, Nasal Polyps diagnostic imaging, Nasal Polyps surgery, Nasopharynx pathology, Nasopharynx surgery, Paranasal Sinus Diseases diagnostic imaging, Paranasal Sinus Diseases surgery, Polyps chemistry, Polyps diagnostic imaging, Polyps pathology, Polyps surgery, Tomography, X-Ray Computed, Cholesterol analysis, Granuloma pathology, Maxillary Sinus pathology, Nasal Polyps pathology, Paranasal Sinus Diseases pathology
- Abstract
Antrochoanal polyps (ACPs) are an infrequent clinical entity. Cholesterol granulomas (CGs) are commonly associated with chronic middle ear disease but are rare in the paranasal sinuses. We describe a case of a 10-year-old girl with a concomitant CG in an ACP which was surgically excised by nasosinusal endoscopic surgery. To our knowledge, there are only five previously published cases of CGs in ACPs and of these, only two were pediatric cases. We describe a third case in the youngest patient yet reported. Increased intrasinus pressure may affect venous and lymphatic drainage, leading to hemorrhages with hemolysis and deposition of cholesterol crystals and their esters initiating the formation of granulomas in the polyp. In addition, the insufficient lymphatic drainage prevents the complete elimination of lipids, contributing to the formation of cholesterol granulomas. The treatment and the outcome of an ACP associated with a CG are the same as for usual ACPs., (Copyright © 2018 Sociedad Española de Anatomía Patológica. Publicado por Elsevier España, S.L.U. All rights reserved.)
- Published
- 2018
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