Literature DB >> 32756056

Juvenile Psammomatoid Ossifying Fibroma of the Orbital Roof: A Rare Cause of Proptosis among Children.

Mohammad Rahmani1, Kasra Hendi1, Saeed Dalfardi1, Amirhossein Larijani1, Maysam Alimohamadi2,3.   

Abstract

INTRODUCTION: Juvenile psammomatoid ossifying fibroma (JPOF) is a rare bone tumor characterized by a predilection for the sinonasal region and a tendency to affect younger patients, with a potential for aggressive growth and high recurrence (30-56%). JPOF warrants complete surgical resection to avoid recurrence. CASE
PRESENTATION: In this article, we report a young boy who presented with unilateral prop-tosis with an expansile bony tumor with ground glass appearance involving the left frontal bone and orbital roof on his images. Complete surgical resection was done, and histopathological examination revealed JPOF with abundant psammomatoid bodies. DISCUSSION: This patient is a rare case of neurocranial JOPF and adds new features to the typical features already described for JPOF.
© 2020 S. Karger AG, Basel.

Entities:  

Keywords:  Orbital tumor; Ossifying fibroma; Proptosis

Mesh:

Year:  2020        PMID: 32756056     DOI: 10.1159/000508691

Source DB:  PubMed          Journal:  Pediatr Neurosurg        ISSN: 1016-2291            Impact factor:   1.162


  2 in total

1.  Psammomatoid ossifying fibroma in the extraconal space: a case report.

Authors:  Hyung Kyung Kim; Soonchan Park; Chang-Woo Ryu
Journal:  Am J Transl Res       Date:  2022-09-15       Impact factor: 3.940

2.  Management and positive outcome of skull-base ossifying fibroma: a case report.

Authors:  Sofia El Akroud; Yao Christian Hugues Dokponou; Mamoune El Mostarchid; Hafsa Chahdi; Abad Cherif El Asri; Miloudi Gazzaz
Journal:  J Surg Case Rep       Date:  2021-07-14
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.