Into the unknown: Navigating orbital cellulitis to reveal retinal metastasis of a hidden primary tumor

Mohammed Abu-Rumaileh, Kashvi Patel, Fahham Asghar
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Abstract

Introduction This is a rare patient presentation of retinal metastasis with an unknown primary tumor.   Case Presentation A 65-year-old woman with a past medical history of left breast carcinoma stage 1 status post left mastectomy in 2014, iron deficiency anemia, anxiety, and depression presented to the emergency department with 1-2 weeks of worsening lower abdominal pain and left-sided chest pain. She also complained of right eye pain, blurry vision, and painful eye movement. Ocular examination demonstrated edema, mild proptosis, conjunctival chemosis, and conjunctival injection. Patient was started on bacitracin ointment and ceftriaxone due to concerns of orbital cellulitis. Ophthalmology was consulted, and their assessment was suggestive of bilateral metastatic neoplastic lesion in retina of both eyes, more pronounced in the right than the left eye. Left supraclavicular lymph node biopsy showed metastatic adenocarcinoma, likely of gastrointestinal or pancreaticobiliary primary. MRI brain was suspicious for calvarial metastatic disease, MRI abdomen showed multiple nodules in the liver suggesting metastases, and whole-body nuclear medicine bone scan suggested possible metastases in the hemithorax and bilateral femurs. After several goals of care discussions, the decision was made by the patient and her family to pursue comfort measures only and she was discharged home with home hospice and later passed away.   Conclusion Retinal metastasis is a rare condition due to the absence of lymphatic system in the eye (1). The most common primary tumors to metastasize to the eye are from breast (47%), lung (21%), and the gastrointestinal tract (4%) (2). In some cases, patients may have no other symptoms (1). Thus, retinal metastasis is important to include in the differential diagnosis, especially for patients with a history of treated primary cancer.
进入未知领域:通过眼眶蜂窝组织炎发现隐藏原发肿瘤的视网膜转移
导读:这是一个罕见的原发肿瘤不明的视网膜转移病例。 病例介绍 一位 65 岁的女性患者,既往病史为 2014 年左侧乳房切除术后左侧乳腺癌 1 期、缺铁性贫血、焦虑和抑郁,因下腹疼痛和左侧胸痛加重 1-2 周来急诊就诊。她还主诉右眼疼痛、视力模糊和眼球活动疼痛。眼部检查显示水肿、轻度突眼、结膜化脓和结膜注射。由于担心发生眼眶蜂窝组织炎,患者开始使用杆菌肽软膏和头孢曲松。眼科专家会诊后认为,双眼视网膜均有转移性肿瘤病变,右眼比左眼更明显。左锁骨上淋巴结活检显示为转移性腺癌,很可能是胃肠道或胰胆管原发癌。脑部核磁共振检查怀疑是颅骨转移性疾病,腹部核磁共振检查显示肝脏有多个结节,提示有转移,全身核医学骨扫描提示半胸和双侧股骨可能有转移。经过多次护理目标讨论后,患者及其家人决定只采取舒适措施,她在家庭临终关怀服务下出院回家,随后去世。 结论 由于眼部没有淋巴系统,视网膜转移是一种罕见的病症(1)。最常见的转移至眼部的原发性肿瘤来自乳腺(47%)、肺(21%)和胃肠道(4%)(2)。在某些情况下,患者可能没有其他症状(1)。因此,将视网膜转移纳入鉴别诊断非常重要,尤其是对有原发性癌症治疗史的患者。
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