Conjunctival stromal tumour: A case report

Jane E. Buys , Christiaan H. Gouws , Stefanus W.D. van der Walt , Jacqueline Goedhals
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Abstract

Conjunctival stromal tumour (COST) is a rare and newly described mesenchymal tumour of the conjunctiva. We present a case of a slow-growing conjunctival lesion in a 54-year-old female. Due to persistent irritant symptoms, the lesion was excised. Histopathological assessment showed a paucicellular tumour set in an oedematous and collagenous background within the lamina propria. Significant nuclear degenerative atypia was noted. Lesional cells were positive for CD34 immunohistochemistry. The features were consistent with COST. The condition is typically unilateral and arises in the bulbar conjunctiva, with both inflammatory and neoplastic origins considered. They are sporadic and occur most frequently in adults. COSTs are indolent and managed effectively with complete surgical excision. Conjunctival myxoma is the most important differential diagnosis due to its association with the Carney complex, a potentially life-threatening condition that requires close clinical follow-up. Accurate recognition of COST and myxoma is crucial to stratify care appropriately.

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结膜基质瘤:病例报告
结膜基质瘤(Conjunctival stromal tumour,COST)是一种新近描述的罕见结膜间质瘤。我们报告了一例生长缓慢的结膜病变,患者是一名 54 岁的女性。由于持续的刺激症状,病变被切除。组织病理学评估显示,固有膜内的水肿和胶原背景中存在一个白细胞瘤。核变性不典型性明显。病变细胞的 CD34 免疫组化呈阳性。这些特征与 COST 一致。这种病通常是单侧的,发生在球结膜,有炎症性和肿瘤性两种起源。该病为散发性,多发于成年人。结膜肌瘤的症状不明显,通过手术完全切除后可得到有效控制。结膜肌瘤是最重要的鉴别诊断,因为它与卡尼综合征有关,卡尼综合征可能危及生命,需要密切的临床随访。准确识别结膜囊肿和肌瘤对于合理分层治疗至关重要。
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