Clinicopathological observation of adult malignant ectodermal mesenchymoma: A case report and literature review.
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RATIONALE: Malignant ectomesenchymoma (MEM) is a relatively rare soft tissue tumor, which predominantly occurs in infants or children under 15 years of age. The classic sites of occurrence are the pelvic perineal region and genitourinary system. Compared to pediatric cases, adult cases exhibit certain differences in clinicopathological features and are more prone to misdiagnosis. A thorough comprehension of their clinicopathologic features is crucial for precise diagnosis and effective management. PATIENT CONCERNS: A 23-year-old male had a lesion located on the right side of his head and face, and the disease course lasted 13 months. A retrospective analysis was conducted on the clinicopathological data, histopathological features, immunophenotype, and molecular pathological changes. DIAGNOSES: The tumor was composed of embryonal rhabdomyosarcoma and undifferentiated neuroectodermal components. Immunohistochemistry showed positivity for rhabdomyosarcoma markers such as Desmin, MyoD1, and Myogenin in the rhabdomyosarcomatous component and positivity for neuroectodermal markers, including synaptophysin and chromogranin A in the neuroectodermal component. No specific molecular alterations were detected in genetic testing. INTERVENTIONS: This is a case of initial misdiagnosis, multimodal comprehensive treatment combining surgery with chemotherapy was the primary therapeutic approach, However, poor clinical outcomes were observed. OUTCOMES: Despite aggressive treatments, the patient died of the disease after 1 year of follow-up. LESSONS: Adult MEM is a biphenotypic sarcoma composed of rhabdomyosarcoma and neuroectodermal tissues. Morphological and immunohistochemical interpretation is crucial for diagnosis. treatment approaches and prognosis are correlated with the completeness of tumor resection and the differentiation degree of both components.