Abstract
BackgroundPrimary 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.Case presentationWe 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.Discussion and conclusionsNone 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.
Highlights
Primary lacrimal sac melanoma is an extremely rare condition with fewer than 50 cases reported so far
MR images show hyperintensity signal on T1-weighted images and hypointense signal on T2-weighted images owing to the paramagnetic properties of melanin
We provide a summarize of the computed tomography (CT) and magnetic resonance imaging (MRI) findings and review previous literature on this condition
Summary
Primary malignant melanoma of the lacrimal sac is a rare condition, with less than 50 cases reported over the past 90 years worldwide. Because our case is a relapsing primary malignant melanoma of the lacrimal sac after surgery, bone destruction may result from the previous dacryorhiocydtostomy. Malignant melanoma of the lacrimal sac may present intermediate signal intensity on T1 and iso-or hypersignal on T2 weighted images in most cases. The differential diagnosis of melanoma in the lacrimal sac considers primary epithelial neoplasms (85.6%), malignant lymphoma (7.8%), neural tumors, inflammatory lesions and metastatic tumor [25]. Based on previous reports and our case, most cases do not present typical signals Reporting such radiological findings is important to create awareness on variant images of primary lacrimal sac melanoma.
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