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Jun, F., Li, L., Ning, L., Yan, L., Siquan, T. and Shixi, L. (2009) Giant laryngeal angioleiomyomas: A case report with review of literature. American Journal of Otolaryngology, 30, 219-220. doi:10.1016/j.amjoto.2008.11.001

has been cited by the following article:

• TITLE: Laryngeal angioleiomyoma: A case report of 52-year-old female

  AUTHORS: Ahmad Rezaee, Leili Ebrahimi, Alireza Sadeghipour, Behzad Sarvar Azimzadeh, Amir Reza Azizian

  KEYWORDS: Laryngeal Angioleiomyoma; Contrast-Enhanced Computed Tomography

  JOURNAL NAME: Case Reports in Clinical Medicine, Vol.2 No.1, March 12, 2013

  ABSTRACT: Introduction: Laryngeal angioleiomyoma is a rare benign tumor of larynx with vascular origin. We report a case of laryngeal angioleiomyoma in a 52-year-old female. Case presentation: A 52- year-old Caucasian female was referred to our institute with a chief compliant of severe midnight snoring. Her symptoms were progressive and began from two years ago. There was no history of hoarseness and laryngeal pain. The patient underwent a laryngoscopic examination and a large mass was seen on the left aryepiglotic fold. Surface of lesion was smooth and covered by laryngeal mucosa with no ulcer. There was a rapid enhancing mass on left aryepiglotic fold with bulging into the left piriformis sinus in contrast-enhanced computed tomography. The tumor was complicated by profuse bleeding after biopsy which was not controlled by conventional approaches. The patient was then administered a general anesthesia and the tumor was completely removed via laryngosurgery accompanied by left superior thyroid artery ligation. The specimen was histopathologically compatible with laryngeal angioleiomyoma. Conclusion: Angioleiomyoma of larynx is of benign nature and rarely recurs. However, it can be complicated by profuse bleeding on biopsy and contrast-medium imaging should be considered before surgical intervention to diagnose the tumor properly and prevent life-threatening complications.