Le pronostic est sombre. Les infections opportunistes, propre au terrain sida aggravent ce pronostic. Perspectives et projets. It is associated with lymph node enlargement, hepatosplenomegaly and fever.
|Published (Last):||25 February 2005|
|PDF File Size:||1.98 Mb|
|ePub File Size:||14.35 Mb|
|Price:||Free* [*Free Regsitration Required]|
Nous rapportons trois observations de maladie de Castleman unicentrique. Castleman disease is a rare disorder of the lymphoid system which can be classified into two clinical groups, monocentric disease versus multicentric disease, and two histological types, the hyaline vascular form versus the plasma cell form. We report three cases of monocentric Castleman disease. The second one is characterized by an uncommon radiological presentation, with a calcification within the tumor.
The third one is a plasma cell form with monoclonal proliferation associated with a monoclonal gammapathy. These three cases highlight the polymorphic clinical and radiological features of Castleman disease. They underlie the difficulty of surgical resection due to the tumor vascularization. Anastasio, L. Jaillard, P. Mariage, B. Journal page Archives Contents list. Article Article Outline. Access to the text HTML. Access to the PDF text.
Recommend this article. Save as favorites. Access to the full text of this article requires a subscription. If you are a subscriber, please sign in 'My Account' at the top right of the screen. Akkad d , B. Bouchindhomme e , N. Tacelli f , J.
Delourme a , b , X. Lafitte a , b , A. Scherpereel a , b , c , M. Remy-Jardin b , f , A. Auteur correspondant. Outline Masquer le plan. Top of the page - Article Outline. Contact Help Who are we? As per the Law relating to information storage and personal integrity, you have the right to oppose art 26 of that law , access art 34 of that law and rectify art 36 of that law your personal data.
You may thus request that your data, should it be inaccurate, incomplete, unclear, outdated, not be used or stored, be corrected, clarified, updated or deleted. Personal information regarding our website's visitors, including their identity, is confidential. The owners of this website hereby guarantee to respect the legal confidentiality conditions, applicable in France, and not to disclose this data to third parties.
You can move this window by clicking on the headline. Observations Observation 1. Masquer le plan.
Une maladie de Hodgkin compliquant l’évolution de la maladie de Castleman
Castleman disease is a group of uncommon lymphoproliferative disorders characterized by lymph node enlargement , characteristic features on microscopic analysis of enlarged lymph node tissue, and a range of symptoms and clinical findings. Research on Castleman disease is rapidly evolving and the disease is becoming better understood. These are differentiated by the number and location of affected lymph nodes and the presence of human herpesvirus 8, a known causative agent. Correctly classifying the Castleman disease subtype is important, as the three subtypes vary significantly in symptoms, clinical findings, disease mechanism, treatment approach, and prognosis. In the United States, approximately 6, to 7, new cases are diagnosed each year. Castleman disease is named after Benjamin Castleman , who first described the disease in
Castleman's disease, also called angiofollicular lymph node hyperplasia was first described as a distinct entity by Castleman et al in Two forms are now described a localized and a multicentric. The clinical and biological signs are varied and heterogeneous, and the diagnostic is made on the histologic examination. This atypical lymphoproliferative disorder is of unknown origin, but interleukin 6 play a central part in this disease. Despite the benignity of this "prelymphoma state", an aggressive course with poor prognosis occur usually in the multicentric form. Malignant lymphomas and Kaposi's sarcoma have been associated with Castleman's disease.
We'd like to understand how you use our websites in order to improve them. Register your interest. Castleman disease CD is rare and is characterized by the existence of a localized form and a multicentric form. The evolution can be marked by the emergence of malignant disease. A year-old man, followed for CD for 20 years, was hospitalized for anemia syndrome, lymphadenopathy of the axillary and sus clavicular lymph nodes and a biological inflammatory syndrome. Histology of the lymph node revealed Hodgkin disease HD rich in lymphocytes. The prevalence of hematologic malignancies in CD is difficult to establish because of the small number of cases reported.