Glaucoma ciliary syndrome: Glaucoma ciliary syndrome. It is a recurrent form of glaucoma combined with ciliary tract infection. It involves one eye, but a few eyes are involved, but not synchronously. The age of onset is 11 to 69 years, but it occurs mostly in young adults. It is often recurrent in the same eye, with intervals of several months to 1 to 2 years. The IOP can be 40-60 mmHg at the time of attack, and the duration of high IOP in each attack is usually 1-14 days, which can recover on its own. There is only mild discomfort during the attack, and even at the peak of the attack, there are no obvious symptoms. Visual acuity is generally normal. The anterior chamber angle is open in a state of high intraocular pressure. Mild ciliary manifestations are present: often within 3 days of the onset of hypertension. No anterior or posterior iris adhesions occur. 1, Atrial aqueous: a few cells floating, atrial flash (-). 2, posterior corneal deposits (KP): grayish white, lambda-like, usually no more than 25, set in the lower l/3 of the cornea or hidden in the atrial trabecular meshwork. kp disappears within a few days to 1 month after IOP returns to normal. KP may or may not reappear when IOP fluctuates. Treatment: Anti-inflammatory and IOP-lowering medications should be used. Surgery is not advisable because it does not prevent its recurrence. However, long-term follow-up should be performed. Surgery should be considered if combined open-angle glaucoma is found and visual function is impaired. Note: 1. Since the disease is self-limiting, most of them have a good prognosis, so it is less harmful than glaucoma. However, if combined with primary open angle glaucoma, irreversible damage to visual function can occur, so it must be taken seriously! You should cooperate with the doctor for further examination and regular routine examination of intraocular pressure, fundus and visual field. 2, corticosteroid drugs should not be used for a long time, so as not to cause hormonal glaucoma.