Castleman's disease. Angiofollicular benign lymph-node hyperplasia. Radiological features in the differential diagnosis of vascular tumours of the pelvis

1979 ◽  
Vol 52 (617) ◽  
pp. 412-414 ◽  
Author(s):  
P. O. Riba
2001 ◽  
Vol 258 (1) ◽  
pp. 42-44 ◽  
Author(s):  
Ü. Osma ◽  
Sebahattin Cureoglu ◽  
Mehmet Yaldiz ◽  
Ismail Topcu

CHEST Journal ◽  
1994 ◽  
Vol 105 (2) ◽  
pp. 637-639 ◽  
Author(s):  
Alfred C. Nicolosi ◽  
G. Hossein Almassi ◽  
Richard Komorowski

1995 ◽  
Vol 59 (5) ◽  
pp. 1162-1165 ◽  
Author(s):  
Joo Hyun Kim ◽  
Tae Gook Jun ◽  
Sook Whan Sung ◽  
Young Soo Shim ◽  
Sung Koo Han ◽  
...  

Blood ◽  
1989 ◽  
Vol 74 (4) ◽  
pp. 1360-1367 ◽  
Author(s):  
K Yoshizaki ◽  
T Matsuda ◽  
N Nishimoto ◽  
T Kuritani ◽  
L Taeho ◽  
...  

Abstract Castleman's disease is a syndrome consisting of giant lymph node hyperplasia with plasma cell infiltration, fever, anemia, hypergammaglobulinemia, and an increase in the plasma level of acute phase proteins. It has been reported that clinical abnormalities disappear after the resection of the affected lymph nodes, suggesting that products of lymph nodes may cause such clinical abnormalities. Interleukin-6 (IL-6) is a cytokine inducing B-cell differentiation to immunoglobulin-producing cells and regulating biosynthesis of acute phase proteins. This report demonstrates that the germinal centers of hyperplastic lymph nodes of patients with Castleman's disease produce large quantities of IL-6 without any significant production of other cytokines. In a patient with a solitary hyperplastic lymph node, clinical improvement and decrease in serum IL-6 were observed following surgical removal of the involved lymph node. There was a correlation between serum IL-6 level, lymph node hyperplasia, hypergammaglobulinemia, increased level of acute phase proteins, and clinical abnormalities. The findings in this report indicate that the generation of IL-6 by B cells in germinal centers of hyperplastic lymph nodes of Castleman's disease may be the key element responsible for the variety of clinical symptoms in this disease.


1996 ◽  
Vol 110 (9) ◽  
pp. 896-898
Author(s):  
Juan P. Rodrigo ◽  
Jose A. Fernandez ◽  
Juan C. Alvarez ◽  
Justo Gómez ◽  
Carlos Suárez

AbstractGiant lymph node hyperplasia (Castleman's disease) is usually reported as a solitary mediastinal tumour, although involvement of other anatomical sites and a multicentric form have been reported. We describe a rare case of Castleman's disease due to its localisation (the left infratemporal fossa) and histology (plasma-cell variant). A brief review of the main clinico-histological characteristics of Castleman's disease is also presented.


2015 ◽  
Vol 9 (1-2) ◽  
pp. 48
Author(s):  
Gökhan Koç ◽  
Hakan Turk ◽  
Sıtkı Un ◽  
Cemal Selcuk Isoglu ◽  
Ferruh Zorlu

Castleman’s disease (CD) is a non-clonal lymph node hyperplasia, mostly seen in the mediastinum. It has various clinical and pathological outcomes. There are different treatments because of its rare occurance and heterogenity. We present 2 cases which were referred to our clinic as retroperitoneal mass and diagnosed as CD after surgical resection.


1991 ◽  
Vol 67 (786) ◽  
pp. 366-370 ◽  
Author(s):  
Y. Baruch ◽  
Y. Ben-Arie ◽  
H. Kerner ◽  
M. Lorber ◽  
L. A. Best ◽  
...  

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