Intraconal Orbital Angioleiomyoma: A Case Report and Review of Literature
author
Abstract:
Purpose: To present a patient with interaconal orbital angioleiomyoma. Case Report: A 22-year-old woman presented with painless slowly progressive proptosis. CT and MRI demonstrated a well-defined Interaconal globe size mass (inferomedially). It was isointense in T1 and T2 weighted and homogenously enhanced by Gadolinium. During the surgery, the tumor was excised via a lateral orbitotomy approach; significant hemorrhage and adhesions to surrounding tissues were noticeable. Histopathologic analysis of the specimen revealed smooth muscle cells with vascular components. IHC assay was positive for SMA and CD34, which confirmed the diagnosis of angioleiomyoma. The patient recovered uneventfully and one year of follow-up showed no recurrence or complications. Conclusion: ALM is an uncommon benign smooth muscle tumor with a vascular component. Orbital involvement (especially interaconal) is extremely rare; caution about considerable intraoperative bleeding and adhesions to surrounding tissue is recommended.
similar resources
Cavernous Sinus Angioleiomyoma: Case Report and Review of the Literature
Cavernous sinus angioleiomyoma (ALM) is extremely rare. Only three cases have been reported to be cavernous sinus ALM, and very few reports described characteristic findings for intracranial ALMs in detail. We report a new case of cavernous sinus ALM, with detailed information on the clinical presentation, radiology, pathology, and surgical approach. A 52-year-old woman had a 6-month history of...
full textAngioleiomyoma of the Hand: A Case Series and Review of the Literature
Background: Angioleiomyomas are rare tumors arising from vascular tissue that can occasionally present in the hand.Reports of angioleiomyomas in this location are highly limited. Here, we describe the presentation and outcomes of aseries of cases of angioleiomyomas.Methods: A retrospective case review of five patients with angioleiomyomas arising in the hand was performed. Pat...
full textProliferating Pilomatricoma: A Case Report and Review of Literature
Proliferating pilomatricoma is a distinctive rare variant of pilomatricoma first described in 1997.Very few cases of proliferating pilomatricoma have been reported in the literature until date. This report is a case of 65 years old male presenting with hard nodular lump on the right side of neck slowly increasing in size for the last 8 months. Wide excision of the lump was performed with clear ...
full textMALAKOPLAKIA OF THE COLON: A CASE REPORT AND LITERATURE REVIEW
Malakoplakia is a rare disease with undefined etiology that has been almost exclusively reported in urology and pathology journals. We are presenting a case of colonic malakoplakia in an I8-year old young man who was referred to us with a four-year history of intermittent rectorrhagia. The pathological examination of the endoscopically resected specimen revealed pathognomonic features of ma...
full textHypoglossal Schowannoma: A Case Report and Review of Literature
Introduction: Schawannomas (neuromas, neurilemmomas) are benign tumors originating from showann cells or nerve fiber sheet cells. They are solitary, encapsulated tumors usually attached to, or surrounded by a nerve. Case Report: We present a case of left hypoglossal nerve schwannoma in a 19 year old man who was admitted with progressive left tongue atrophy. Conclusion: Schwannoma of the hy...
full textEosinophilic Cellulitis: Report of a case and literature review
Eosinophilic cellulitis is a rare skin disorder may be idiopathic or be associated with other conditions. We present a 42- year- old female patient with bilateral atypical cellulitis – like lesions on her arms. The patient had a documented infection with Leptospira recently, and had a positive history for fascioliasis two years before.Histopathology examination of the l...
full textMy Resources
Journal title
volume 25 issue 2
pages 137- 141
publication date 2019-12
By following a journal you will be notified via email when a new issue of this journal is published.
No Keywords
Hosted on Doprax cloud platform doprax.com
copyright © 2015-2023