Key result
A 68-year-old woman with a primary uterine tumor was diagnosed with the extremely rare myxoid variant of malignant fibrous histiocytoma using electron microscopy and immunohistochemistry.
Case Report (n=1)
Highlights the cytologic features of a rare primary uterine myxoid malignant fibrous histiocytoma and the importance of immunohistochemistry and electron microscopy for accurate diagnosis.
Consider rare uterine myxoid MFH in atypical masses; case report leaves open larger studies on prognosis and management.
BACKGROUND: Primary malignant fibrous histiocytoma (MFH) of the uterus is extremely rare. The 10 cases reported in the literature all involved the pleomorphic variant, and to the best of our knowledge, the myxoid variant has not been reported before. We describe the cytologic findings of primary uterine myxoid MFH in relation to the myxoid component, potentially leading to an incorrect diagnosis. CASE: A 68-year-old woman presented with a primary uterine tumor. Endometrial cytology showed numerous loosely arranged, spindle-shaped fibroblastlike cells; atypical histiocytelike cells; and giant cells with a necrotic background. The overall cytologic picture was of a degenerated pleomorphic leiomyosarcoma with an inconclusive diagnosis. A diagnosis of myxoid MFH was established after electron microscopic and immunohistochemical studies of the primary tumor and tumor transplanted, as primary cultured cells, in nude mice. The patient underwent an exploratory laparotomy and died of tumor progression 38 days after the initial consultation, without treatment. CONCLUSION: Because of overlapping cytologic features among uterine sarcomas with myxoid stroma, it is important to recognize the histiocytic lineage of tumor cells by immunohistochemistry and electron microscopy in various presentations of fresh samples.
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Kiyozuka et al. (2001) conducted a case report in Primary uterine myxoid malignant fibrous histiocytoma (n=1). Cytologic examination, electron microscopy, and immunohistochemistry was evaluated on Diagnosis of myxoid malignant fibrous histiocytoma. A 68-year-old woman with a primary uterine tumor was diagnosed with the extremely rare myxoid variant of malignant fibrous histiocytoma using electron microscopy and immunohistochemistry.
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