Literature DB >> 12782827

A case of paranasal sinus angiolipoma.

Travis J Pfannenstiel1, Mark Boseley, Latonia Roach.   

Abstract

OBJECTIVE: To present the first documented case of an angiolipoma of the maxillary sinus, our treatment of the patient, and the 1-year follow-up results. At the conclusion of the report, the reader should be able to discuss the incidence, treatment options, and long-term prognosis of angiolipomas of the paranasal sinuses. STUDY
DESIGN: A case study reporting on a single patient with the diagnosis of maxillary sinus angiolipoma.
METHODS: Review of diagnostic studies, the operative technique, and the patient's chart for the 1-year period after treatment.
RESULTS: The patient remains free of disease 1 year after definitive surgical treatment.
CONCLUSIONS: Angiolipomas are exceedingly rare in this location. The accepted treatment for this disease in other regions of the body consists of wide local excision with close follow-up. The extent of the disease found in this patient required a medial maxillectomy for en bloc resection. We would advocate such an approach for other physicians who are faced with a patient with this rare diagnosis.

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Year:  2003        PMID: 12782827     DOI: 10.1097/00005537-200306000-00031

Source DB:  PubMed          Journal:  Laryngoscope        ISSN: 0023-852X            Impact factor:   3.325


  4 in total

1.  Angiolipoma larynx: a case report.

Authors:  Devinder Rai; Sarika Verma
Journal:  Indian J Otolaryngol Head Neck Surg       Date:  2011-06-26

Review 2.  Rectal angiolipoma: a case report and review of literature.

Authors:  Sabite Kacar; Sedef Kuran; Tulay Temucin; Bulent Odemis; Nilufer Karadeniz; Nurgul Sasmaz
Journal:  World J Gastroenterol       Date:  2007-03-07       Impact factor: 5.742

3.  Cellular infiltrative angiolipoma of cheek in an infant.

Authors:  Ajoy Kumar Shahi; Hiralal Ash; Kabita Chatterji; Revati Singh
Journal:  Natl J Maxillofac Surg       Date:  2014 Jul-Dec

4.  Massive noninfiltrating angiolipoma of the buccal mucosa: Report of an extremely rare case.

Authors:  Srikanth Dhanala; Nagaraju Tanneru
Journal:  J Oral Maxillofac Pathol       Date:  2017 Jan-Apr
  4 in total

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