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CASE REPORT
Year : 2022  |  Volume : 19  |  Issue : 4  |  Page : 251-253

Congenital sacrococcygeal rhabdomyosarcoma


Department of Pathology, NRI Medical College, Guntur, Andhra Pradesh, India

Correspondence Address:
Dr. Renuka Venkata Inuganti
Department of Pathology, NRI Medical College, Chinakakani, Guntur - 522 503, Andhra Pradesh
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ajps.ajps_69_21

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Rhabdomyosarcoma (RMS) is one of the common malignant soft-tissue sarcomas affecting children. It originates from the embryonic mesenchyme precursor of striated muscle and is frequently seen in the head-and-neck region, genitourinary system and extremities. Occasionally, it arises from the retroperitoneum, biliary tract and abdomen and is rarely seen in the sacrococcygeal area. A 4-month-male child presented with a nodule over the sacrum. Based on histopathology and immunohistochemical marker studies, a final diagnosis of RMS was rendered. There was no evidence of any teratomatous elements.


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