O'Donnell B A, Martin F J, Kan A E, Filipic M
Sydney Eye Hospital, Woolloomooloo, New South Wales.
Aust N Z J Ophthalmol. 1990 May;18(2):211-3. doi: 10.1111/j.1442-9071.1990.tb00616.x.
There have been nine previously reported cases of intraocular lacrimal gland choristoma. This case report is of an infant with an intraocular lacrimal gland choristoma which was managed conservatively for a 19-month period until the onset of glaucoma. Tumour biopsy was initially performed because until this time the tumour's behaviour suggested it was not malignant. The latter was confirmed on biopsy, however hypotony resulted following the surgical intervention.
此前已有9例眼内泪腺迷离瘤的报道。本病例报告的是一名患有眼内泪腺迷离瘤的婴儿，该患儿在19个月的时间里接受了保守治疗，直至青光眼发作。最初进行了肿瘤活检，因为在此之前肿瘤的表现提示其并非恶性。然而活检证实为恶性，且手术干预后出现了低眼压。
