Geremew Teketel Tadesse, Zewdie Woldie Jember, Nisiro Abebe Melis, Engida Ghion Getenet, Tesgera Tigist Gutema
Department of Pathology, Hawassa University Comprehensive Specialized Hospital, Hawassa, Sidama, Ethiopia.
Department of Pathology, Worabe Comprehensive Specialized Hospital, Ethiopia.
Int J Surg Case Rep. 2025 Jan;126:110812. doi: 10.1016/j.ijscr.2024.110812. Epub 2024 Dec 30.
Orbital lymphomas, are extranodal lymphomas primarily involving the ocular adnexa, which includes conjunctiva, eyelids, eyelashes, eyebrows, lacrimal glands, retro-orbital soft tissues, and the extraocular muscles. Ocular adnexal lymphomas can be primary or secondary. This case is important because there are few case reports in the world, and it is among the first case to be reported from Ethiopia.
Our case is a 32-year-old female patient from the Ethiopia who has presented with painless slowly growing conjuctival mass over the left eye. Histopathologic and IHC examination confirm the diagnosis of primary conjuctival small lymphocytic lymphoma (SLL).
The majority of Ocular adnexal lymphomas are unilateral, with bilateral lesions occurring in about 7 %-24 % of all cases. Ocular adnexal lymphomas are mostly low-grade B-cell non-Hodgkin lymphomas, with approximately half being extranodal marginal zone B-cell lymphomas, with small lymphocytic lymphomas being much less common. The treatment options include radiotherapy, immunotherapy, chemotherapy, or a combination of these treatments. The gold standard treatment of isolated conjunctival lymphoma after resection is localized external-beam radiation therapy.
SLLs of the ocular adnexa are rare, especially in the conjunctiva, with few cases reported in the published literature. The treating physician's should consider primary lymphomas are a possible cause of salmon colored mass in the conjunctiva specially those having history of chronic conjunctivitis. Histopathology with immunohistochemistry confirms the diagnosis of ocular lymphoma.
眼眶淋巴瘤是主要累及眼附属器的结外淋巴瘤,眼附属器包括结膜、眼睑、睫毛、眉毛、泪腺、眶后软组织和眼外肌。眼附属器淋巴瘤可为原发性或继发性。该病例很重要,因为世界上病例报告较少,且是埃塞俄比亚报告的首批病例之一。
我们的病例是一名来自埃塞俄比亚的32岁女性患者,左眼出现无痛性缓慢生长的结膜肿物。组织病理学和免疫组化检查确诊为原发性结膜小淋巴细胞淋巴瘤(SLL)。
大多数眼附属器淋巴瘤为单侧,双侧病变约占所有病例的7%-24%。眼附属器淋巴瘤大多为低级别B细胞非霍奇金淋巴瘤,约一半为结外边缘区B细胞淋巴瘤,小淋巴细胞淋巴瘤则少见得多。治疗选择包括放疗、免疫疗法、化疗或这些治疗方法的联合应用。孤立性结膜淋巴瘤切除术后的金标准治疗是局部外照射放疗。
眼附属器的SLL罕见,尤其是在结膜,已发表文献中报告的病例很少。治疗医生应考虑原发性淋巴瘤是结膜出现鲑鱼色肿物的可能原因,特别是那些有慢性结膜炎病史的患者。组织病理学检查及免疫组化可确诊眼淋巴瘤。