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Familial hypercholesterolemia with bilateral cholesterol granuloma: A case series. | LitMetric

Familial hypercholesterolemia with bilateral cholesterol granuloma: A case series.

Int J Surg Case Rep

Otorhinolaryngology and Head & Neck Surgery Department, Main Hospital, King Fahad Medical City, P.O. Box. 59046, Riyadh 11525, Saudi Arabia. Electronic address:

Published: July 2019

Introduction: Cholesterol granuloma is a benign mass that commonly involves the petrous apex but rarely affects other structures, such as the mastoid cavity. It is diagnosed histologically by the presence of giant cells, and Its management is individualized based on some factors such as the size and location of the lesion.

Presentation Of Case: The first case was a 33-year-old man who presented to the outpatient clinic with a two-year history of right-sided pulsatile tinnitus, hearing loss, and vertigo. Upon investigations, a large, destructive mass in the tympanomastoid region was found and managed surgically. The other case was for a 41-year-old man who presented to the emergency department with loss of consciousness. Urgent CT was done and revealed an aggressive hypodense posterior fossa mass destroying the right temporal bone that was managed surgically.

Discussion: In this report, we describe two patients with familial hypercholesterolemia who developed bilateral cholesterol granuloma that were managed surgically.

Conclusion: These cases are reported because of their rare location and presentation since few cases of bilateral cholesterol granuloma have been reported in the literature.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6734150PMC
http://dx.doi.org/10.1016/j.ijscr.2019.07.018DOI Listing

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