Gross perianal embryonal rhabdomyosarcoma with severe multiple bone metastases throughout the body: a case report.

Abstract

In adults, embryonal rhabdomyosarcoma (ERMS) is rare and has a poor prognosis. Giant perianal ERMS with severe multiple bone metastases at initial diagnosis has not been reported and lacks effective treatment options. This current case report describes a 31-year-old female patient that presented with a large lump on the right side of the anus. ERMS was diagnosed, accompanied by multiple bone metastases throughout the body and severe thrombocytopenia. She had an extremely low platelet count at initial diagnosis, making systemic chemotherapy inappropriate. Genetic testing did not help identify effective targeted drugs. A multi-target tyrosine kinase inhibitor, anlotinib, was selected to control the tumours combined with local radiotherapy to relieve pain. The lump became smaller and this reduction was maintained for 5 months. At 7 months after the diagnosis, the patient died of thrombocytopenia. This current case may provide supportive evidence for a potential treatment for patients with advanced ERMS, especially those not suitable for chemotherapy or surgery.

• Authors: Jing-Jing Lu, Min-Bin Chen, Xiao-Jiao Gao, Yan Zhang, Yuan-Yuan Liu, Yang Yong, Ping Li
• Journal: The Journal of international medical research (J Int Med Res) Vol. 50 Issue 3 Pg. 3000605221087050 (Mar 2022) ISSN: 1473-2300 [Electronic] England
• PMID: 35317622 (Publication Type: Case Reports, Journal Article)

Topics

• Adult
• Anal Canal (pathology)
• Bone Neoplasms (secondary)
• Female
• Humans
• Rhabdomyosarcoma, Embryonal (drug therapy, genetics, pathology)