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Sporadic Malignant Triton Tumor of Shoulder: a Case Report.
Al-Alwan, Mohammad; Noar, Ghaith Abu; Al-Alwan, Ayat; Alrwabdeh, Sura; Etawi, Mahmood.
Affiliation
  • Al-Alwan M; Orthopedic Department at Royal Rehabilitation Center at King Hussein Medical Center, Amman, Jordan.
  • Noar GA; Orthopedic Department at Royal Rehabilitation Center at King Hussein Medical Center, Amman, Jordan.
  • Al-Alwan A; Radiology Department at King Hussein Medical Center, Amman, Jordan.
  • Alrwabdeh S; Histopathology Department at King Hussein Medical Center, Amman, Jordan.
  • Etawi M; Orthopedic Department at Royal Rehabilitation Center at King Hussein Medical Center, Amman, Jordan.
Med Arch ; 78(2): 174-176, 2024.
Article de En | MEDLINE | ID: mdl-38566863
ABSTRACT

Background:

Malignant triton tumors (MTT) are subtype of malignant peripheral nerve sheath tumor (MPNST) which develop from Schwan cells of peripheral nerves or within neurofibromas, and shows rhabdomyoblastic differentiation. It is a rare soft tissue tumor with poor prognosis.

Objective:

We report a case of Malignant Triton Tumor (MTT) arising in the right shoulder in a 46 year old male patient presented to our Musculoskeletal Oncology Clinic at Royal Rehabilitation center at King Hussein Medical Center during June 2018. Case presentation The patient was complaining of an 8 months long progressive right shoulder pain and swelling at the posterior lateral area of the shoulder. As accurate diagnosis is crucial in such case, investigations that included x-rays and magnetic resonance imaging (MRI) demonstrated an soft tissue tumor involving the right shoulder area leading to the differential diagnosis of aggressive soft tissue tumor which laid down the plan of an open incisional biopsy to be reported histopathological as a case of Malignant Triton Tumor which is a very rare and aggressive sarcoma originates from the peripheral nerve sheaths as it is subtype of malignant peripheral nerve sheath tumors after which excision of the entire tumor with safety margin was performed and referred for adjuvant chemotherapy.

Conclusion:

The treatment of choice is radical tumor excision with wide margins followed by chemotherapy and /or radiotherapy to improve the 5 years survival rates.
Sujet(s)
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Tumeurs cutanées / Tumeurs des tissus mous / Neurofibrosarcome / Neurinome Limites: Humans / Male / Middle aged Langue: En Journal: Med Arch Année: 2024 Type de document: Article Pays d'affiliation: Jordanie Pays de publication: Bosnie-Herzégovine

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Tumeurs cutanées / Tumeurs des tissus mous / Neurofibrosarcome / Neurinome Limites: Humans / Male / Middle aged Langue: En Journal: Med Arch Année: 2024 Type de document: Article Pays d'affiliation: Jordanie Pays de publication: Bosnie-Herzégovine