Published online Sep 26, 2023. doi: 10.12998/wjcc.v11.i27.6476
Peer-review started: March 31, 2023
First decision: July 3, 2023
Revised: July 16, 2023
Accepted: August 2, 2023
Article in press: August 2, 2023
Published online: September 26, 2023
Processing time: 173 Days and 10 Hours
An unusual case of acute acquired concomitant esotropia (AACE) with congenital paralytic strabismus in the right eye is reported.
A 23-year-old woman presented with complaints of binocular diplopia and esotropia of the right eye lasting 4 years and head tilt to the left since 1 year after birth. The Bielschowsky head tilt test showed right hypertropia on a right head tilt. She did not report any other intracranial pathology. A diagnosis of AACE and right congenital paralytic strabismus was made. Then, she underwent medial rectus muscle recession and lateral rectus muscle resection combined with inferior oblique muscle myectomy in the right eye. One day after surgery, the patient reported that she had no diplopia at either distance or near fixation and was found to be orthophoric in the primary position; furthermore, her head posture immediately and markedly improved.
In future clinical work, in cases of AACE combined with other types of strabis
Core Tip: Clinically, in cases of older children, adults, or even the elderly with sudden diplopia accompanied by simultaneous or subsequent esotropia, acute acquired concomitant esotropia (AACE) should be considered after excluding intracranial space-occupying lesions and vascular diseases. In recent years, the diagnosis and treatment of AACE have improved considerably, and until now no one has reported any case of AACE combined with other types of strabismus either in China or abroad. Here, we report one case of AACE with congenital paralytic strabismus.
