PubMed Health⌕ Search
Home/Archive/PubMed

PubMed · 16754223

Fronto-ethmoidal mucocele after coronal orbital decompression.

Hanneke W Mensink·Dion Paridaens
View original source ↗Export metadata ↓

Abstract

A patient who underwent coronal orbital decompression for Graves' orbitopathy eight years earlier presented with left-sided proptosis without signs of periorbital inflammation. Computed tomography imaging showed a fronto-ethmoidal mucocele. It is suggested that this mucocele may be a late complication of decompression surgery.

Explore related subjects

Decompression, SurgicalEthmoid SinusExophthalmosFemaleFrontal SinusGraves OphthalmopathyHumansMiddle AgedMucoceleParanasal Sinus DiseasesTomography, X-Ray ComputedCase ReportsJournal Article

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Hanneke W Mensink, Dion Paridaens. 2006. Fronto-ethmoidal mucocele after coronal orbital decompression.. https://doi.org/10.1080/01676830600674510

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

PubMed2007

Combined ventral and dorsal surgery for myelopathy and myeloradiculopathy.

The past decade has witnessed significant advances in the surgical treatment of cervical myelopathy and myeloradiculopathy. In this article, we discuss in detail the indications for combined ventral and dorsal surgery for the treatment of cervical myelopathy and myeloradiculopathy. In addition, the advances in surgical technique and instrumentation in cervical spine surgery are explored. Finally, complication avoidance and management strategies are discussed. Combined ventral and dorsal decompression, reconstruction, and instrumentation procedures are viable options in the treatment of a select group of patients with complex cervical myelopathy or myeloradiculopathy.

Decompression, Surgical↗
PubMed2006

Multifocal Langerhans cell histiocytosis of the pediatric spine: a case report and literature review.

CASE REPORT: An 11-month-old boy presented with a 3-month history of lower extremity weakness. CT and MRI of the spine revealed an enhancing epidural mass, extending from T1 through T5 and exiting through multiple foramina. The largest extraspinal extent was located at the T3 vertebral level and was accompanied by complete T3 vertebral collapse. A second lytic lesion at the L2 vertebral body without an obvious enhancing mass was also noted. Open biopsy and decompression of the spinal cord were performed, and histopathological analysis revealed a mixed inflammatory lesion with abundant S-100 and CD1a immunoreactive Langerhans cells consistent with the diagnosis of Langerhans cell histiocytosis (LCH). DISCUSSION: The authors present a very rare pediatric case of spinal LCH causing spinal cord compression. Possible clues to early detection, consideration of differential diagnoses, and a brief literature review are presented.

Decompression, Surgical↗