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首页> 外文期刊>BMC Ophthalmology >CT and MRI findings in relapsing primary malignant melanoma of the lacrimal sac: a case report and brief literature review
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CT and MRI findings in relapsing primary malignant melanoma of the lacrimal sac: a case report and brief literature review

机译:CT和MRI调查结果在翻转泪囊的原发性恶性黑色素瘤:案例报告和简短的文献综述

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Primary lacrimal sac melanoma is an extremely rare condition with fewer than 50 cases reported so far. Clinically, its symptoms resemble those of dacryocystitis, leading to frequent misdiagnosis. During diagnosis, imaging examination is often performed to differentiate tumors from inflammation. In this report, we present a case of primary lacrimal sac melanoma and summarize the CT and MRI characteristics of lacrimal sac melanoma. We report a 50-year-old female patient who had undergone a dacryocystectomy for the left lacrimal sac mass. Postoperative pathological examination confirmed the presence of primary malignant melanoma. Three months later, a lump in the lacrimal sac area was found. The patient underwent CT and MR examinations. CT scan demonstrated a partially well-defined soft mass in the fossa of left lacrimal sac extending into the nasolacrimal duct and anterior ethmoid sinus. MRI revealed an intermediate signal intensity on T1 and iso-or hyper-signal on T2 weighted images. Histopathological examination on biopsy confirmed recurrence of primary lacrimal sac melanoma. None has described the CT and MR findings of primary lacrimal sac melanoma so far. Typically, MR images show hyperintensity signal on T1-weighted images and hypointense signal on T2-weighted images owing to the paramagnetic properties of melanin. In contrast to previous reports and the present case, most cases do not present these typical signals. Thus, reporting such radiological findings is important to create awareness on variant images of primary lacrimal sac melanoma. This will reduce misdiagnosis and mistreatment.
机译:原发性泪囊囊马洲瘤是一个极少数罕见的病症,迄今为止报告的少于50例。临床上,其症状类似于泪囊炎的症状,导致频繁的误诊。在诊断过程中,通常进行成像检查以区分肿瘤免受炎症。在本报告中,我们提出了一种原发性泪囊囊马曼诺的案例,并总结了泪囊囊马野瘤的CT和MRI特征。我们举报了一个50岁的女性患者,为左泪囊囊囊切除了泪囊切除术。术后病理检查证实了原发性恶性黑色素瘤的存在。三个月后,发现了泪囊区域的肿块。病人接受了CT和先生检查。 CT扫描证明左泪囊的窝中的部分明确定义的软质量延伸到鼻升降管道和前乙状体鼻窦中。 MRI在T2加权图像上揭示了T1和ISO或超信号的中间信号强度。体检的组织病理学检查证实原发性泪囊囊黑色素瘤的复发。到目前为止,没有描述原发性泪囊囊黑素瘤的CT和先生。通常,由于黑色素素的顺磁性特性,MR图像在T1加权图像和T2加权图像上的低压信号上显示出高度信号信号。与先前的报告和当前情况相比,大多数情况下都不呈现这些典型信号。因此,报告此类放射发现对于创造对原发性泪囊囊瘤的变异图像的认识是重要的。这将减少误诊和虐待。

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