Case Report: Primary Squamous Cell Carcinoma of the Orbit in a Patient With Carney's Syndrome Treated With Multidisciplinary Approaches

IF 1.5 Q4 ONCOLOGY Cancer reports Pub Date : 2024-09-26 DOI:10.1002/cnr2.70020
Md. Arifur Rahman, Rajesh Balakrishnan, Mohammad Golam Mostofa, Mohammed Rashedul Islam, Enamul Kabir, Md. Shariful Islam, Bidoura Naznin, Arunangshu Das, Qamruzzaman Chowdhury
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Abstract

Background

Squamous cell carcinoma (SCC) is a rare malignancy of invasive epithelium with keratinocyte differentiation, and it is the most common form of eyelid malignant neoplasm, comprising 5%–10% of malignancies. While SCC rarely affects the orbit, it may be involved through local invasion from a cutaneous primary site or extension by perineural invasion. Only 12 cases of primary orbital SCC have been reported until now. Here, we present a case of primary carcinoma of the right orbit with coexisting Carney's syndrome, a rare genetic disorder associated with multiple endocrine neoplasias (MEN) syndromes.

Case

A 62-year-old South Asian male presented with a painful swelling in the lateral aspect of the right eyebrow and protrusion of the eyeball in August 2020. He had a history of excision of Right atrial Myxoma in March 2020. Orbital computerized tomography (CT) and positron emission tomography (PET-CT) scans revealed an enhancing soft tissue lesion in the right orbit with the involvement of frontal and ethmoid sinuses. Biopsy confirmed HPV-related poorly differentiated SCC, positive for HPV-related markers. The patient received concurrent chemo irradiation with Cisplatin. Follow-up PET-CT done 3 months later showed a new lesion appeared in the right orbital region and right lobe of thyroid. Later had surgical excision and total thyroidectomy, and histopathological examination (HPE) from orbit was reported as invasive SCC and from the thyroid was reported as synchronous papillary thyroid cancer. The patient's proptosis resolved, and subsequent PET-CT and magnetic resonance imaging (MRI) scans did not show any residual or recurrent disease.

Conclusion

Primary SCC of the orbit is an extremely rare disease, and this case report presents the 13th reported case and the first one associated with Carney's syndrome. As there is no standard treatment regimen for primary SCC of the orbit, this case highlights the use of multimodality treatment, including surgical excision and chemo irradiation. The findings emphasize the importance of early detection and management of this uncommon and life-threatening condition, providing hope for patients and aiding in the prevention of recurrence.

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病例报告:采用多学科方法治疗卡尼氏综合征患者的眼眶原发性鳞状细胞癌
背景 鳞状细胞癌(SCC)是一种罕见的具有角质细胞分化的浸润性上皮恶性肿瘤,是眼睑恶性肿瘤中最常见的一种,占恶性肿瘤的 5%-10%。虽然 SCC 很少累及眼眶,但它可能通过皮肤原发部位的局部侵袭或神经周围侵袭的扩展而累及眼眶。迄今为止,仅有12例原发性眼眶SCC的报道。在此,我们介绍一例右眼眶原发性癌并发卡尼氏综合征的病例,卡尼氏综合征是一种罕见的遗传性疾病,与多发性内分泌肿瘤(MEN)综合征有关。 病例 一名 62 岁的南亚男性于 2020 年 8 月因右眉毛外侧肿胀疼痛和眼球突出而就诊。他曾于 2020 年 3 月接受过右心房肌瘤切除术。眼眶计算机断层扫描(CT)和正电子发射计算机断层扫描(PET-CT)显示,右眼眶软组织病变增强,额窦和乙状窦受累。活组织检查证实患者为HPV相关的分化不良SCC,HPV相关标记物阳性。患者同时接受了顺铂化疗照射。3 个月后进行的 PET-CT 随访显示,右眼眶和甲状腺右叶出现了新的病变。后来进行了手术切除和甲状腺全切除,眼眶的组织病理学检查(HPE)报告为浸润性 SCC,甲状腺的组织病理学检查(HPE)报告为同步性甲状腺乳头状癌。患者的突眼症状消失,随后的 PET-CT 和磁共振成像(MRI)扫描也未显示任何残留或复发疾病。 结论 眼眶原发性 SCC 是一种极为罕见的疾病,本病例报告是第 13 例,也是第一例与卡尼氏综合征相关的病例。由于眼眶原发性 SCC 尚无标准治疗方案,本病例强调了多模式治疗的使用,包括手术切除和化学照射。研究结果强调了早期发现和治疗这种不常见且危及生命的疾病的重要性,为患者带来了希望,并有助于预防复发。
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来源期刊
Cancer reports
Cancer reports Medicine-Oncology
CiteScore
2.70
自引率
5.90%
发文量
160
审稿时长
17 weeks
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