Cervical Castleman disease in children

Lai-ping Zhong1, Guan-fu Chen, Shi-fang Zhao

  • 1Department of Oral and Maxillofacial Surgery, College of Medicine, Second Affiliated Hospital, Zhejiang University, No. 88 Jiefang Road, Hangzhou 310009, China. zhonglp@hotmail.com

Insights

A rare cervical Castleman disease (hyaline vascular type) case in a child compressed the carotid artery. Surgical removal was successful, with no recurrence after six months, offering a positive outlook for this rare tumor.

Area of Science:

  • Pediatric Oncology
  • Vascular Surgery
  • Head and Neck Pathology

Background:

  • Castleman disease is a rare lymphoproliferative disorder with unknown etiology.
  • The hyaline vascular subtype is the most common variant, typically affecting the mediastinum.
  • Cervical involvement, particularly in pediatric patients, is exceptionally rare.

Observation:

  • A 6-year-old child presented with a cervical mass.
  • Computed tomography and magnetic resonance angiography revealed a mass compressing the right common carotid artery bifurcation.
  • Intraoperative findings included four masses tightly adherent to the carotid artery and jugular vein.

Findings:

  • Surgical excision of the cervical Castleman disease was performed using blunt dissection.
  • Histopathological analysis confirmed the hyaline vascular subtype.
  • No signs of recurrence were observed at the 6-month postoperative follow-up.

Implications:

  • This case highlights the importance of considering rare diagnoses like Castleman disease in pediatric cervical masses.
  • Successful surgical management can be achieved even with vascular encasement.
  • Further research is needed to understand the long-term prognosis and optimal treatment strategies for pediatric cervical Castleman disease.

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