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1 Introduction Thyroblastoma is a newly recognized entity, included in the 5th Edition WHO Classification of Endocrine and Neuroendocrine Tumors, and is molecularly defined by DICER1 mutations [1]. Histologically, it shows complex multilineage features, including fetal-type thyroid follicles, fetal-type glands, a primitive blastemal component, and spindle cell stroma with possible rhabdomyoblastic differentiation [1].
This case report describes a rare case of nodal low grade serous pelvic neoplasia. Together with histological correlation, it illustrates previously undocumented cytomorphological features and also discusses important differential diagnosis and potential pitfalls for misdiagnosis.
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