Rhabdomyosarcoma of the head and neck in children: Review and update

被引:47
作者
Reilly, Brian K. [1 ]
Kim, AeRang [2 ]
Pena, Maria T. [3 ]
Dong, Tiffany A. [4 ]
Rossi, Christopher [5 ]
Murnick, Jonathan G. [6 ]
Choi, Sukgi S. [7 ,8 ]
机构
[1] George Washington Univ, Med Ctr, Childrens Natl Med Ctr, Div Otolaryngol, Washington, DC 20010 USA
[2] Childrens Natl Med Ctr, Ctr Canc & Blood Disorder, Washington, DC 20010 USA
[3] Childrens Natl Med Ctr, Washington, DC 20010 USA
[4] George Washington Univ, Med Ctr, Washington, DC 20037 USA
[5] Childrens Natl Med Ctr, Dept Pathol, Washington, DC 20010 USA
[6] Childrens Natl Med Ctr, Dept Diagnost Imaging & Radiol, Washington, DC 20010 USA
[7] Childrens Hosp Pittsburgh, Pediat Otolaryngol, Pittsburgh, PA 15213 USA
[8] Univ Pittsburgh, Sch Med, Otolaryngol, Pittsburgh, PA USA
关键词
Rhabdomyosarcoma; Head and neck cancer; Pediatric neck mass; Second-look; Parameningeal; Non-parameningeal; INTERGROUP RHABDOMYOSARCOMA; CHILDHOOD RHABDOMYOSARCOMA; SURVIVAL; ADULTS;
D O I
10.1016/j.ijporl.2015.06.032
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Objective: To review the clinical presentation, histology, staging, treatment modalities, and survival for pediatric head and neck rhabdomyosarcoma (non-orbital). Study design: Retrospective chart review at a tertiary pediatric hospital of children treated over 18 years (1996-2014) for primary head and neck non-orbital rhabdomyosarcoma. Methods: Medical charts were examined for clinical presentation, staging, histology, genetic abnormalities, treatment modalities, recurrence and complications from treatment. Results: Our cohort was 17 children (7 male, 10 female) with rhabdomyosarcoma with a median age of 6.3 years (range <1-19). The majority of tumors were of parameningeal location (13117) with embryonal histology (11/17). Twenty-nine percent (5/17) demonstrated advanced metastatic disease at initial referral. Fifty-three percent (9/17) had skull base erosion and/or cranial nerve deficits. PET CT scan was performed in 4 patients. The overall survival was 75% for the duration of the study. Primary surgical excision was performed in all 4 patients with nonparameningeal tumors as compared to only 1 patient with a parameningeal tumor. All received chemotherapy and radiotherapy, as none had completely resectable disease. Conclusion: Pediatric non-orbital primary rhabdomyosarcoma of the head and neck usually has a rapid onset and presents with advanced disease. Our analysis found that the majority of patients in our series had a cranial neuropathy at presentation, which highlights how advanced the disease is in these patients at presentation. The first mode of surgical intervention should be directed toward biopsy in junction with a metastatic work-up. Primary excision with negative microscopic margins for nonparameningeal rhabdomyosarcoma is ideal to spare radiotherapy but was not achievable in our cohort. The benefits of second-look biopsy after chemotherapy and radiation are still unproven; however, we believe that it was beneficial in two patients in our review for further resection thus decreasing subsequent radiation. Fluorodeoxy-D-glucose positron emission tomography (PET) to evaluate disease post treatment may further define the role for second look surgery. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
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收藏
页码:1477 / 1483
页数:7
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