Inflammatory Myofibroblastic Tumor of the Upper Airways Harboring a New TRAF3-ALK Fusion Transcript

被引:7
作者
Di Ruscio, Valentina [1 ]
Mastronuzzi, Angela [1 ]
Russo, Ida [1 ]
Neri, Marianna [2 ]
Stracuzzi, Alessandra [3 ]
Giovannoni, Isabella [3 ]
Tropiano, Maria Luisa [4 ]
De Ioris, Maria Antonietta [1 ]
Milano, Giuseppe Maria [1 ]
机构
[1] Bambino Gesu Pediat Hosp, IRCCS, Dept Hematol Oncol Cell & Gene Therapy, Piazza St Onofrio 4, Rome 00165, Italy
[2] Annunziata Hosp, Pediat Unit, Via Migliori 1, Cosenza 87100, Italy
[3] Bambino Gesu Pediat Hosp, IRCCS, Pathol Unit, Piazza SantOnofrio 4, Rome 00165, Italy
[4] Bambino Gesu Pediat Hosp, IRCCS, Dept Pediat Surg, Airway Surg Unit, Piazza SantOnofrio 4, Rome 00165, Italy
来源
CHILDREN-BASEL | 2021年 / 8卷 / 06期
关键词
inflammatory myofibroblastic tumor; children; ALK inhibitors; LARGE-CELL LYMPHOMA; SOFT-TISSUE; RARE-CAUSE; PSEUDOTUMOR; LUNG; ALK; CRIZOTINIB; TRACHEA; EXPRESSION; EXPERIENCE;
D O I
10.3390/children8060505
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Inflammatory myofibroblastic tumor (IMT) is a rare disease that mainly involves the lung and the abdomen with an intermediate clinical course but a recurrence rate between 15-30%. Radical surgery represents the gold standard of treatment, while chemotherapy and radiotherapy are considered for unresectable lesions. The identification of ALK translocations in IMT opened the option for the use of target therapies. Indeed, the ALK inhibitors have changed the treatment approach for aggressive lesions, improving the prognosis. Intraluminal upper-way IMT is extremely rare and represents a medical challenge. We reported an endotracheal IMT case presenting a previously unknown TRAF3-ALK fusion transcript.
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收藏
页数:7
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