Queen Victoria Hospital, East Grinstead, United Kingdom.
King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia.
Ophthalmic Plast Reconstr Surg. 2020 Nov/Dec;36(6):540-544. doi: 10.1097/IOP.0000000000001621.
To review the clinical and histopathological findings associated with ectopic lacrimal gland tissue.
A systematic review of the literature on ectopic lacrimal gland tissue was performed. Studies which met clinical and histolopathological criteria for ectopic lacrimal gland tissue written in English and published in peer-reviewed journals were included.
Sixty-nine publications detailing 180 cases of ectopic lacrimal gland tissue were published between 1946 and 2018. Males were affected slightly more than females (57% vs. 43%) and 95% cases were unilateral. Patients presented at a mean age of 21 years, most commonly with a mass, although orbital lesions commonly presented with proptosis. The most common location for ectopic lacrimal gland tissue was epibulbar conjunctiva (62%), other locations included orbital (16%), eyelid (11%), intraocular (9%), lacrimal sac (2%), and nasal mucosa (0.6%) sites. Most lesions (86%) were locally resected. The most common histological types were complex choristomas (56%) and simple choristomas (38%). However, neoplastic transformation to pleomorphic adenoma (5%), adenocystic carcinoma (0.6%), and adenocarcinoma (0.6%) was reported.
Ectopic lacrimal gland tissue is rare but should be considered in the differential diagnosis of masses in the epibulbar conjunctiva, eyelid, orbit, and lacrimal sac, particularly in childhood, as the diverse way it presents means that it may mimic more common choristomas. It can undergo neoplastic transformation in the same way as can the lacrimal gland and incomplete excision can result in recurrence.We review the clinical and histopathological findings associated with ectopic lacrimal gland tissue. Ectopic lacrimal gland tissue is susceptible to neoplastic transformation in the same way as is the lacrimal gland.Supplemental Digital Content is available in the text.
回顾与异位泪腺组织相关的临床和组织病理学发现。
对异位泪腺组织的文献进行系统回顾。纳入符合临床和组织病理学标准的、用英文撰写并发表在同行评议期刊上的异位泪腺组织研究。
1946 年至 2018 年间共发表了 69 篇详细描述 180 例异位泪腺组织的文献。男性略多于女性(57%比 43%),95%的病例为单侧。患者的平均发病年龄为 21 岁,最常见的表现是肿块,尽管眼眶病变常表现为眼球突出。异位泪腺组织最常见的部位是球结膜(62%),其他部位包括眼眶(16%)、眼睑(11%)、眼内(9%)、泪囊(2%)和鼻黏膜(0.6%)。大多数病变(86%)经局部切除。最常见的组织学类型是复杂的先天性组织瘤(56%)和单纯先天性组织瘤(38%)。然而,也有报道发生多形性腺瘤(5%)、腺样囊性癌(0.6%)和腺癌(0.6%)的肿瘤性转化。
异位泪腺组织罕见,但在鉴别诊断球结膜、眼睑、眼眶和泪囊的肿块时应考虑到,尤其是在儿童中,因为其表现形式多种多样,可能会模仿更常见的先天性组织瘤。它可以像泪腺一样发生肿瘤性转化,不完全切除可能导致复发。我们回顾了与异位泪腺组织相关的临床和组织病理学发现。异位泪腺组织与泪腺一样容易发生肿瘤性转化。补充数字内容可在文本中查看。