Jain Asha S, Duncan Nicole B, Potter Heather D, Burkat Cat N, Warner Evan J
The University of Wisconsin School of Medicine and Public Health, Madison, WI, 53705, USA.
The Department of Ophthalmology and Visual Sciences, University of Wisconsin-Madison, Madison, WI, 53705, USA.
Am J Ophthalmol Case Rep. 2024 Jun 8;35:102089. doi: 10.1016/j.ajoc.2024.102089. eCollection 2024 Sep.
This report describes the clinical and histological characteristics and management of a keratinized lesion of the palpebral conjunctiva in a 59-year-old male. The lesion was identified as a rare acantholytic variant of squamous cell carcinoma that atypically arose from a non-sun exposed region of palpebral conjunctiva. Management was complete excision via Mohs surgery.
A 59-year-old male presented with ocular irritation and chronic foreign body sensation in the right eye. Exam revealed a keratinized lesion in the right lower tarsal conjunctiva, and an initial shave biopsy was non-diagnostic. 12 months later, the patient presented with similar symptoms and a larger, more irregular lesion for which histopathology of a tarsal-involving excisional biopsy was consistent with acantholytic squamous cell carcinoma with involved margins. The patient subsequently underwent complete excision via Mohs surgery and a secondary reconstruction.
Acantholytic variants of squamous cell carcinoma are rare and are described as arising from areas with routine sun exposure. This case reports such a lesion arising from non-sun exposed tarsal conjunctiva, as identified by histopathology of a full-thickness excisional biopsy. The lesion was successfully managed with complete excision via Mohs surgery and secondary reconstruction. Given that this histologic variant may be more aggressive and have higher rates of recurrence than other forms of squamous cell carcinoma, this case highlights the importance of complete excisional biopsy and accurate histopathology of concerning periocular lesions and offers a template for management of similar lesions. The unique presenting location should bring awareness to consideration of this type of malignancy developing on palpebral conjunctiva.
本报告描述了一名59岁男性睑结膜角化病变的临床、组织学特征及治疗情况。该病变被确定为鳞状细胞癌的一种罕见棘层松解变体,非典型地起源于睑结膜非阳光暴露区域。治疗方法为通过莫氏手术进行完整切除。
一名59岁男性因右眼眼部刺激和慢性异物感就诊。检查发现右下睑结膜有角化病变,初次削切活检未明确诊断。12个月后,患者出现类似症状,病变更大且更不规则,累及睑板的切除活检组织病理学检查结果符合伴有切缘受累的棘层松解性鳞状细胞癌。患者随后通过莫氏手术进行了完整切除及二期重建。
鳞状细胞癌的棘层松解变体罕见,通常被描述为起源于经常暴露于阳光的区域。本病例报告了这样一个起源于非阳光暴露的睑板结膜的病变,通过全层切除活检的组织病理学检查得以确定。该病变通过莫氏手术完整切除及二期重建成功治疗。鉴于这种组织学变体可能比其他形式的鳞状细胞癌更具侵袭性且复发率更高,本病例强调了对可疑眼周病变进行完整切除活检及准确组织病理学检查的重要性,并为类似病变的治疗提供了模板。其独特的发病部位应引起对睑结膜发生此类恶性肿瘤的关注。