CASTLEMAN DISEASE IN CHILDREN: DIAGNOSIS AND TREATMENT

DOI: 10.38103/jcmhch.2020.64.11

  • Dinh Viet Hung
  • Nguyen Thi Thu Thao
  • Le Tho Duc
  • Nguyen Minh Tuan
  • Dao Trung Hieu
Keywords: Castleman disease, angiofollicular lymph node hyperplasia, giant lymph node hyperplasia, lymph node hamartoma

Abstract

Background: We describe the experiences in diagnosis and results of treatment in pediatric Castleman
disease.
Method: Serial case reports.
Result: From 2016 to 2019, we had 7 cases of pediatric Castleman disease: 3 boys and 4 girl. The
median age at diagnosis was 147 months (121-173 months). Clinical manifestations were found in five
cases. They were all unicentric Castleman disease (6 abdominal mass, one left infraclavicular mass). All
patients were operated with postoperative period uneventful. The median time of postoperative follow up
was 22.7 months (11-53 months) with no signs of relapse.
Conclusions: Pediatric Castleman disease is a rare benign lymph node hyperplasia, it can be localised
or disseminated. Operation is the treatment of choice for localised Castleman disease.

điểm /   đánh giá
Published
2020-09-04
Section
Case Report