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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.
Abstract:
We report a new case of cervical Castleman disease (hyaline vascular type) in a 6-year-old child. The mass was shown on computed tomography and magnetic resonance angiography (MRA) to be compressing the bifurcation of the right common carotid artery. At operation four masses were found, which were tightly adherent to both the artery and the right jugular vein. These were removed by blunt dissection and there were no signs of recurrence after 6 months. This is a rare tumour (we know of only 24 other reports), which is usually asymptomatic, and of uncertain prognosis.
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