Congenital sacrococcygeal rhabdomyosarcoma.
| Autor: | Inuganti RV; Department of Pathology, NRI Medical College, Guntur, Andhra Pradesh, India., Boddapati A; Department of Pathology, NRI Medical College, Guntur, Andhra Pradesh, India., Mathi A; Department of Pathology, NRI Medical College, Guntur, Andhra Pradesh, India., Shaik R; Department of Pathology, NRI Medical College, Guntur, Andhra Pradesh, India. |
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| Jazyk: | angličtina |
| Zdroj: | African journal of paediatric surgery : AJPS [Afr J Paediatr Surg] 2022 Oct-Dec; Vol. 19 (4), pp. 251-253. |
| DOI: | 10.4103/ajps.ajps_69_21 |
| Abstrakt: | 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. Competing Interests: None |
| Databáze: | MEDLINE |
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