Orbital Mass in a Patient With Exacerbation of Chronic Migraine – A Case Report

2019 ◽  
Vol 60 (1) ◽  
pp. 274-275
Author(s):  
Kelly H. Yom ◽  
Aaron M. Ricca ◽  
Audrey C. Ko
Keyword(s):  
Case Report ◽  
Chronic Migraine ◽  
Orbital Mass

scholarly journals The Relief Effects of Ramelteon on Refractory Chronic Migraine: A Case Report

2016 ◽  
Vol 14 (4) ◽  
pp. 405-406 ◽  
Author(s):  
Yi-Cheng Hou ◽  
Chien-Han Lai
Keyword(s):  
Case Report ◽  
Chronic Migraine ◽  
Refractory Chronic Migraine

Periocular thelaziasis presenting as an orbital mass – a case report

Orbit ◽  
2019 ◽  
Vol 38 (6) ◽  
pp. 503-506
Author(s):  
Kirthi Koka ◽  
Andrea Tongbram ◽  
Bipasha Mukherjee ◽  
Raman Muthusamy ◽  
Azhahia Nambi ◽  
...  
Keyword(s):  
Case Report ◽  
Orbital Mass

scholarly journals P02.01: Glial peri-orbital heterotopia: a rare type of peri-orbital mass: a case report and a literature review

2018 ◽  
Vol 52 ◽  
pp. 141-141
Author(s):  
E. di Pasquo ◽  
M. Kuleva ◽  
P. Sonigo ◽  
A. Millischer ◽  
D. Bremond-Gignac ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Rare Type ◽  
Orbital Mass

The “Ram's Horns Sign”: A Case Report of an Unusual Side Effect of OnabotulinumtoxinA in a Chronic Migraine Patient

2016 ◽  
Vol 56 (10) ◽  
pp. 1656-1658 ◽  
Author(s):  
Antonio Russo ◽  
Marcello Silvestro ◽  
Alessandro Tessitore ◽  
Gioacchino Tedeschi
Keyword(s):  
Case Report ◽  
Chronic Migraine ◽  
Side Effect ◽  
Migraine Patient

scholarly journals A Rare Presentation of Retinoblastoma as a Fungating Orbital Mass: A Case Report

2020 ◽  
Vol 10 (3) ◽  
pp. 298-302
Author(s):  
Kenan Kıbıcı ◽  
Berrin Erok ◽  
Onat Akın
Keyword(s):  
Case Report ◽  
Rare Presentation ◽  
Orbital Mass

scholarly journals Orbital myeloid sarcoma misdiagnosed for subperiostal hematoma: a case report

2021 ◽  
Vol 15 (1) ◽  
Author(s):  
Bahaa Razem ◽  
Mohamed Raiteb ◽  
Sanaa El Mrini ◽  
Faiçal Slimani
Keyword(s):  
Acute Myeloid Leukemia ◽  
Case Report ◽  
Myeloid Leukemia ◽  
De Novo ◽  
Myeloid Sarcoma ◽  
Orbital Mass ◽  
Genetic Features ◽  
Immature Myeloid Cells ◽  
Acute Myeloid

Abstract Background Myeloid sarcoma is a solid tumor that consists of immature myeloid cells occurring at an extramedullary site. It can present before, concurrent with, or after the diagnosis of acute myeloid leukemia or other myeloproliferative diseases, and a proportion of patients never develop bone marrow infiltration. Only a few isolated cases of pediatric orbital myeloid sarcoma have been reported, and they are often associated with a high misdiagnosis rate. Case report We report a rare case of pediatric orbital myeloid sarcoma associated with blunt trauma in a 3-year-old Caucasian male patient, which was clinically and radiologically misdiagnosed for orbital subperiostal hematoma. The patient underwent a surgical intervention to drain the hematoma when an orbital mass was found. The microscopic, immunologic, and genetic features of the tumor and the myelogram were in favor of LAM2, and the patient was started with chemotherapy with a favorable evolution within 18 months follow-up. Conclusion Orbital myeloid sarcoma usually exhibits clinical and radiological features that can be easily misleading, especially if it happens de novo or as the first manifestation of acute myeloid leukemia. Only a few isolated cases have reported and proposed trauma as a trigger event of the onset of this type of tumor proliferation, but further investigations and evidence are needed to support this hypothesis.

Rare presentation of Adenoid cystic carcinoma presenting as retro-orbital mass: a case report

2017 ◽  
Vol 01 (02) ◽  
Author(s):  
Vinaya kumar Muttagi ◽  
Munish Gairola ◽  
Parveen Ahlawat ◽  
Archana Aggarwal ◽  
Kanika Sharma ◽  
...  
Keyword(s):  
Case Report ◽  
Adenoid Cystic Carcinoma ◽  
Rare Presentation ◽  
Orbital Mass ◽  
Adenoid Cystic

scholarly journals Chronic migraine and chiropractic rehabilitation: A case report

2003 ◽  
Vol 2 (2) ◽  
pp. 55-59 ◽  
Author(s):  
R. Clark Davis
Keyword(s):  
Case Report ◽  
Chronic Migraine
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