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Pott’s Puffy Tumor in an Adult Female: A Case Report in a Rare Demographic

Pott’s puffy tumor (PPT) is a localized forehead swelling with underlying subperiosteal abscess formation and osteomyelitis of the frontal bone. It is a rare complication of frontal sinusitis, and it is especially rare in adult females. A careful review of existing literature identified only 17 case...

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Detalles Bibliográficos
Autores principales: Hitt, Nathaniel, Rosengren, Tyler, Delaney, Thomas, Dettmer, Timothy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9187141/
https://www.ncbi.nlm.nih.gov/pubmed/35698718
http://dx.doi.org/10.7759/cureus.24922
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author Hitt, Nathaniel
Rosengren, Tyler
Delaney, Thomas
Dettmer, Timothy
author_facet Hitt, Nathaniel
Rosengren, Tyler
Delaney, Thomas
Dettmer, Timothy
author_sort Hitt, Nathaniel
collection PubMed
description Pott’s puffy tumor (PPT) is a localized forehead swelling with underlying subperiosteal abscess formation and osteomyelitis of the frontal bone. It is a rare complication of frontal sinusitis, and it is especially rare in adult females. A careful review of existing literature identified only 17 cases in adult females. Treatment requires antibiotic therapy and often surgical drainage/debridement. Here, we present a case of a 76-year-old female diagnosed with PPT. She was placed on amoxicillin-clavulanate 875 mg twice daily for six weeks. Her symptoms resolved with the antibiotic course, and she is scheduled for otolaryngology (ENT) follow-up, including dedicated sinus computed tomography (CT). While Pott’s puffy tumor is a rare manifestation of chronic sinusitis, it is important to recognize and treat to avoid serious intracranial complications.
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spelling pubmed-91871412022-06-12 Pott’s Puffy Tumor in an Adult Female: A Case Report in a Rare Demographic Hitt, Nathaniel Rosengren, Tyler Delaney, Thomas Dettmer, Timothy Cureus Internal Medicine Pott’s puffy tumor (PPT) is a localized forehead swelling with underlying subperiosteal abscess formation and osteomyelitis of the frontal bone. It is a rare complication of frontal sinusitis, and it is especially rare in adult females. A careful review of existing literature identified only 17 cases in adult females. Treatment requires antibiotic therapy and often surgical drainage/debridement. Here, we present a case of a 76-year-old female diagnosed with PPT. She was placed on amoxicillin-clavulanate 875 mg twice daily for six weeks. Her symptoms resolved with the antibiotic course, and she is scheduled for otolaryngology (ENT) follow-up, including dedicated sinus computed tomography (CT). While Pott’s puffy tumor is a rare manifestation of chronic sinusitis, it is important to recognize and treat to avoid serious intracranial complications. Cureus 2022-05-11 /pmc/articles/PMC9187141/ /pubmed/35698718 http://dx.doi.org/10.7759/cureus.24922 Text en Copyright © 2022, Hitt et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Internal Medicine
Hitt, Nathaniel
Rosengren, Tyler
Delaney, Thomas
Dettmer, Timothy
Pott’s Puffy Tumor in an Adult Female: A Case Report in a Rare Demographic
title Pott’s Puffy Tumor in an Adult Female: A Case Report in a Rare Demographic
title_full Pott’s Puffy Tumor in an Adult Female: A Case Report in a Rare Demographic
title_fullStr Pott’s Puffy Tumor in an Adult Female: A Case Report in a Rare Demographic
title_full_unstemmed Pott’s Puffy Tumor in an Adult Female: A Case Report in a Rare Demographic
title_short Pott’s Puffy Tumor in an Adult Female: A Case Report in a Rare Demographic
title_sort pott’s puffy tumor in an adult female: a case report in a rare demographic
topic Internal Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9187141/
https://www.ncbi.nlm.nih.gov/pubmed/35698718
http://dx.doi.org/10.7759/cureus.24922
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