Journals / Erciyes Medical Journal / 2020 / Cilt: 42 - Sayı: 3

Ganglioneuroblastoma: A Rare Tumor in Parapharyngeal Space

Pages
339–342
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

A multidisciplinary approach is especially important in such kind of rare tumors.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Background: Ganglioneuroblastoma is a malignant tumor, usually found in the adrenal glands, retroperitoneal ganglions or posterior mediastinum.
📊
Key Findings & Data:Case Report: A 5-year-old girl was admitted to the pediatrics clinic with the complaint of a mass on the right side of her neck for about six months.
💡
Conclusion & Impact:A multidisciplinary approach is especially important in such kind of rare tumors.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Özet

Background: Ganglioneuroblastoma is a malignant tumor, usually found in the adrenal glands, retroperitoneal ganglions or posterior mediastinum. In the head and neck region, Ganglioneuroblastoma is presented as a sub-type of neuroblastoma that originated from the sympathetic chain. It is often found in the retropharyngeal area, and if it involves the neck region, it is often found in the carotid space posterior to vascular sheat. Case Report: A 5-year-old girl was admitted to the pediatrics clinic with the complaint of a mass on the right side of her neck for about six months. Ultrasonography was carried out as an initial diagnostic tool, and it revealed a solid homogeneous mass. As a second-line diagnostic imaging method, Magnetic Resonance Imaging (MRI) was performed. The T2 weighted MRI sections showed a hyperintense mass was observed with an axial diameter of 37×40 mm and a craniocaudal diameter of 6 cm in the right parapharyngeal and prevertebral space. Although fine-needle aspiration biopsy (FNAB) was the first preferred biopsy method for neck masses, the FNAB report was inadequate. An incisional biopsy was carried out, and the pathology report described the tumor as ganglioneuroma. There were no immature/neuroblastic components in the serial sections. The patient was operated on transcervically. In the final pathology report, the tumor was described as ganglioneuroblastoma, intermixed type. After multidisciplinary consultations, the patient is still being followed with no further additional chemotherapy or radiotherapy. Conclusion: Ganglioneuroblastoma is a rare tumor in the parapharyngeal region. A multidisciplinary approach is especially important in such kind of rare tumors.

🔖

Cite This Article

ULU, Ş., KINAR, A., BUCAK, A. (2020). Ganglioneuroblastoma: A Rare Tumor in Parapharyngeal Space. Erciyes Medical Journal, Cilt: 42 - Sayı: 3, 339–342. https://ajindex.com/articles/213567

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (8)

  1. Kuet ML, Kasbekar AV, Masterson L, Jani P. Management of tumors arising from the parapharyngeal space: A systematic review of 1,293 cases reported over 25 years. Laryngoscope 2015; 125(6): 1372–81
  2. Manjaly JG, Alexander VR, Pepper CM, Ifeacho SN, Hewitt RJ, Hartley BE. Primary cervical ganglioneuroblastoma. Int J Pediatr Otorhinolaryngol 2015; 79(7): 1007–12
  3. Bluestone CD, Simons JP, Healy GB. Bluestone and Stool’s pediatric otolaryngology. 5th edition. USA: People’s Medical Publishing House; 2014.p.1711–823
  4. Basaran B, Polat B, Unsaler S, Ulusan M, Aslan I, Hafiz G. Parapharyngeal space tumours: the efficiency of a transcervical approach without mandibulotomy through review of 44 cases. Acta Otorhinolaryngol Ital 2014; 34(5): 310–6
  5. Ansarin M, Tagliabue M, Chu F, Zorzi S, Proh M, Preda L. Transoral robotic surgery in 6. Lee HS, Kim J, Lee HJ, Koh YW, Choi EC. Transoral robotic surgery for neurogenic tumors of the prestyloid parapharyngeal space. Auris Nasus Larynx 2012; 39(4): 434–7
  6. Lu D, Liu J, Chen Y, Chen F, Yang H. Primary cervical ganglioneuroblastoma: A case report. Medicine (Baltimore) 2018; 97(12): e0090
  7. Gauchan E, Sharma P, Ghartimagar D, Ghosh A. Ganglioneuroblastoma in a newborn with multiple metastases: a case report. J Med Case Rep 2017; 11(1): 239
  8. Bolzacchini E, Martinelli B, Pinotti G. Adult onset of ganglioneuroblastoma of the adrenal gland: case report and review of the literature. Surg Case Rep 2015; 1: 79.