1.Sequential treatment with siltuximab and tocilizumab for childhood idiopathic multicentric Castleman disease: a case report.
Ping YI ; Xing-Xing ZHANG ; Tian TANG ; Ying WANG ; Xiao-Chuan WU ; Xing-Fang LI
Chinese Journal of Contemporary Pediatrics 2025;27(5):613-617
The patient, an 11-year-old girl, was admitted with recurrent fever for 20 days, worsening with abdominal distension for 7 days. Upon admission, she presented with recurrent fever, lymphadenopathy, hepatosplenomegaly, polyserositis, and multiple organ dysfunction. Lymph node pathology and clinical manifestations confirmed the diagnosis of idiopathic multicentric Castleman disease-TAFRO syndrome. Treatment with siltuximab combined with glucocorticoids was initiated, followed by maintenance therapy with tocilizumab. The patient is currently in complete clinical remission. Therefore, once a child is diagnosed with idiopathic multicentric Castleman disease -TAFRO syndrome, early use of siltuximab should be considered for rapid disease control, followed by tocilizumab for maintenance therapy.
Humans
;
Castleman Disease/drug therapy*
;
Child
;
Antibodies, Monoclonal, Humanized/administration & dosage*
;
Female
;
Antibodies, Monoclonal/administration & dosage*
2.Treatment of Idiopathic Multicentric Castleman's Disease With Sequential Thalidomide-Cyclophosphamide-Prednisone After Siltuximab:Report of One Case.
Yue DANG ; Jian LI ; Ya-Ping LUO ; Lu ZHANG
Acta Academiae Medicinae Sinicae 2025;47(3):483-486
Castleman's disease is a rare polyclonal lymphoproliferative disorder.This article reports the diagnosis and treatment of a 45-year-old female patient with idiopathic multicentric Castleman's disease.The patient presented recurrent fever,enlarged lymph nodes,and elevated levels of inflammation markers.After multiple serological examinations and tissue biopsies,she was diagnosed with hyaline vascular-type Castleman's disease.Initially,the patient received siltuximab targeting interleukin-6,which significantly improved her condition.Considering the cost and convenience of long-term treatment,she subsequently switched the therapy to an oral treatment regimen of thalidomide,cyclophosphamide,and prednisone (TCP),which maintained disease control.This report aims to highlight the diagnostic complexity and diversity of treatment options for idiopathic multicentric Castleman's disease,demonstrating the potential of the TCP regimen as a cost-effective treatment choice.
Humans
;
Castleman Disease/drug therapy*
;
Female
;
Middle Aged
;
Thalidomide/therapeutic use*
;
Prednisone/therapeutic use*
;
Cyclophosphamide/therapeutic use*
;
Antibodies, Monoclonal/administration & dosage*
4.IgG4-related sclerosing disease mimicking Castleman's disease: report of a case.
Quanhong QIN ; Mingfang ZHANG ; Zhiqi YIN ; Zhandong HU
Chinese Journal of Pathology 2014;43(3):194-195
Antineoplastic Combined Chemotherapy Protocols
;
therapeutic use
;
Castleman Disease
;
immunology
;
pathology
;
Cyclophosphamide
;
therapeutic use
;
Diagnostic Errors
;
Doxorubicin
;
therapeutic use
;
Humans
;
Immunoglobulin G
;
blood
;
Kidney
;
Lymph Node Excision
;
Lymph Nodes
;
pathology
;
surgery
;
Lymphatic Diseases
;
drug therapy
;
immunology
;
pathology
;
surgery
;
Male
;
Middle Aged
;
Nephrectomy
;
Pancreas
;
Plasma Cells
;
immunology
;
pathology
;
Prednisone
;
therapeutic use
;
Submandibular Gland
;
Vincristine
;
therapeutic use
6.Evolvement in pathogen factor and pathogenesis of Castleman's disease.
Yi ZHANG ; Gan-di LI ; Wei-ping LIU
Chinese Journal of Pathology 2005;34(12):812-815
Antiviral Agents
;
therapeutic use
;
Castleman Disease
;
drug therapy
;
metabolism
;
pathology
;
virology
;
Dendritic Cells, Follicular
;
pathology
;
Herpesviridae Infections
;
virology
;
Herpesvirus 8, Human
;
isolation & purification
;
Humans
;
Interleukin-6
;
blood
;
Receptor, Epidermal Growth Factor
;
metabolism

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