Treatment and outcome of Unicentric Castleman Disease: a retrospective analysis of 71 cases.


Journal

British journal of haematology
ISSN: 1365-2141
Titre abrégé: Br J Haematol
Pays: England
ID NLM: 0372544

Informations de publication

Date de publication:
07 2019
Historique:
received: 08 01 2019
accepted: 26 02 2019
pubmed: 25 4 2019
medline: 27 5 2020
entrez: 25 4 2019
Statut: ppublish

Résumé

We retrospectively analysed 71 cases of Unicentric Castleman disease, a rare, usually asymptomatic, benign lymphoproliferative disorder presenting as a unique nodal mass. Although surgery is considered as the gold standard therapy, only 38 patients (54%) underwent initial surgical resection and 95% were cured. An additional 9 patients had surgery after an attempt at medical reduction. Reduction therapy was used in 21 patients with a 55% response rate, but without evidence for an optimal regimen. Radiotherapy was limited to 8 patients because of associated toxicity. Watch and wait was considered in 13 asymptomatic patients and 11 of these remained stable for up to 17 years.

Identifiants

pubmed: 31016730
doi: 10.1111/bjh.15921
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

269-273

Informations de copyright

© 2019 British Society for Haematology and John Wiley & Sons Ltd.

Auteurs

David Boutboul (D)

Department of Clinical Immunology, Hôpital Saint-Louis, Assistance Publique Hôpitaux de Paris (APHP), Paris, France.
National Reference Centre for Castleman Disease (CRMdC), Paris, France.
UMR1149 CRI INSERM-Université Paris Diderot, Paris, France.
Université Paris Diderot, Paris 7, Paris, France.

Jehane Fadlallah (J)

Department of Clinical Immunology, Hôpital Saint-Louis, Assistance Publique Hôpitaux de Paris (APHP), Paris, France.
Université Paris Diderot, Paris 7, Paris, France.

Sylvain Chawki (S)

Department of Clinical Immunology, Hôpital Saint-Louis, Assistance Publique Hôpitaux de Paris (APHP), Paris, France.

Claire Fieschi (C)

Department of Clinical Immunology, Hôpital Saint-Louis, Assistance Publique Hôpitaux de Paris (APHP), Paris, France.
Université Paris Diderot, Paris 7, Paris, France.
Inserm U1126, Centre Hayem, Hôpital Saint-Louis, Paris, France.

Marion Malphettes (M)

Department of Clinical Immunology, Hôpital Saint-Louis, Assistance Publique Hôpitaux de Paris (APHP), Paris, France.
EA3518, Université Paris Diderot, Paris 7, Paris, France.

Antoine Dossier (A)

Department of Internal Medicine, Hôpital Bichat, Assistance Publique Hôpitaux de Paris (APHP), Paris, France.

Laurence Gérard (L)

Department of Clinical Immunology, Hôpital Saint-Louis, Assistance Publique Hôpitaux de Paris (APHP), Paris, France.
National Reference Centre for Castleman Disease (CRMdC), Paris, France.
EA3518, Université Paris Diderot, Paris 7, Paris, France.

Pierre Mordant (P)

Université Paris Diderot, Paris 7, Paris, France.
INSERM, UMR-S1152, Hôpital Bichat, Université Paris Diderot, Paris 7, Paris, France.
Division of Thoracic and vascular surgery, Hôpital Bichat, Paris, France.

Véronique Meignin (V)

National Reference Centre for Castleman Disease (CRMdC), Paris, France.
Department of Pathology, Hôpital Saint-Louis, Assistance Publique Hôpitaux de Paris (APHP), Paris, France.

Eric Oksenhendler (E)

Department of Clinical Immunology, Hôpital Saint-Louis, Assistance Publique Hôpitaux de Paris (APHP), Paris, France.
National Reference Centre for Castleman Disease (CRMdC), Paris, France.
Université Paris Diderot, Paris 7, Paris, France.
EA3518, Université Paris Diderot, Paris 7, Paris, France.

Lionel Galicier (L)

Department of Clinical Immunology, Hôpital Saint-Louis, Assistance Publique Hôpitaux de Paris (APHP), Paris, France.
National Reference Centre for Castleman Disease (CRMdC), Paris, France.
EA3518, Université Paris Diderot, Paris 7, Paris, France.

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Classifications MeSH