Introduction Presence of two primary malignancies is rare and occurs in 3-5% of the cancer patients. As per our extensive internet research, this is the only reported case of a synchronous sino-nasal embryonal rhabdomyosarcoma with squamous cell carcinoma-tongue. The case report is important because of the rare diagnosis and the challenge we faced in the diagnosis and treatment of the pat...

Introduction: Rhabdomyosarcoma is a high-grade malignant neoplasm with skeletal muscle differentiation; common soft tissue sarcoma in children but considered one of the rarest adults. Case description: We report case 35-year-old male chronic productive cough and haemoptysis for five days. A CT scan nasopharynx revealed blocked left maxillary ethmoid sinus bone destruction. These findings raised...

Rhabdomyosarcoma is the most common soft-tissue sarcoma that is most typically found in children under 15 years of age (1). The World Health Organization distinguishes predominantly pleomorphic, alveolar, embryonal and mixed types of rhabdomyosarcoma (2). Head and neck rhabdomyosarcoma is common in childhood, however, is very rare in adults, especially of the embryonal type in the nasal cavity ...

Rhabdomyosarcoma is a soft tissue sarcoma arising from cells of myogenic lineage. They can be divided into Embryonal rhabdomyosarcoma (ERMS), Alveolar rhabdomyosarcoma (ARMS) and Pleomorphic rhabdomyosarcoma. ARMS occurs in 10-25years age group and the most common sites being extremities, perirectal and perineal regions, head and neck region is frequently involved in childhood but is exceedingl...

Sinonasal tumors often mimick inflammatory diseases. If misdiagnosed, results are life threatening. This article comprises of study done on 5 patients who presented with nasal mass. They underwent clinical examination, diagnostic endoscopy, radiology and histopathological examination (HPE). Thorough evaluation helps the surgeon diagnose rare cases thus preventing detrimental outcomes. Herein we...

Rhabdomyosarcoma (RMS) is a fast growing, malignant tumour arising from immature mesenchymal cells, committed to skeletal muscle differentiation. It is more often seen in the paediatric population and constitutes less than 1% of all malignancies and less than 3% of all soft tissue tumours. RMS of the paranasal sinuses constitutes 10-15% of adult head and neck RMS, ethmoidal and maxillary sinuse...

Nasal chondromesenchymal hamartoma (NCMH) is a rare nasal benign tumor, which arises from the nasal cavity or paranasal sinuses. In this article, we present a five-year-old male patient with rhabdomyosarcoma unity in remission that emerged with nasal obstruction. Synchronous diagnosis of pediatric tumors such as pleuropulmonary blastoma in the literature is a remarkable finding. We found a mass...

Abstract Rhabdomyosarcoma is the most common sarcoma of childhood, and this tumor third neoplasm after neuroblastoma nephroblastoma. Rhabdomyosarcomas may originate in any anatomical site, occurring predominantly head neck regions, orbits, skull base, nasal cavity, nasopharynx, where there little or no musculoskeletal tissue. The involvement ear mastoid bone rhabdomyosarcoma uncommon. embryonal...

We report a case of extensive paranasal sinus and orbit rhabdomyosarcoma (RMS) with intra-cranial invasion treated successfully with chemotherapy and radiotherapy. A 13-years-old male patient complained of painless and progressive proptosis of his left eye for two weeks. Ocular examination showed elevated intraocular pressure, limited extraocular movement, proptosis, and conjunctival ciliary in...