A rare case with a radiological malpractice claim: Castleman's disease

2018 ◽  
Vol 138 (1-2) ◽  
Author(s):  
Cem Terece ◽  
Sibel Çağlar Atacan ◽  
Kağan Gürpinar
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.


2007 ◽  
Vol 14 (12) ◽  
pp. 1098-1100 ◽  
Author(s):  
Koji. Hatano ◽  
Shigeki Fujita ◽  
Yuichi Tsujimoto ◽  
Tsuyoshi Takada ◽  
Masato Honda ◽  
...  

2015 ◽  
Vol 6 (1) ◽  
pp. 20-22
Author(s):  
Pratik Dipak Shah ◽  
Srijon Mukherji ◽  
Yogendra Chauhan

ABSTRACT Castleman's disease (CD) is a rare, benign disease of unknown cause that induces reactive lymph node hyperplasia. The disease was first defined by Dr Benjamin Castleman. It is an unusual cause of a neck mass. The goal of this paper is to report a rare case of Castleman's disease at unusual site (level IB) and discuss its management. How to cite this article Shah PD, Chauhan Y, Mukherji s. Castleman's Disease: An Orphan Lymphoproliferative Disorder. Int J Head Neck Surg 2015;6(1):20-22.


2018 ◽  
Vol 23 (4) ◽  
pp. 344-346
Author(s):  
Erbil Karaman ◽  
Çağrı Ateş ◽  
Ali Kolusarı ◽  
İsmet Alkış ◽  
Hanım Güler Şahin ◽  
...  

2019 ◽  
Vol 12 (3) ◽  
pp. 885-889
Author(s):  
Kota Shimokihara ◽  
Takashi Kawahara ◽  
Ryo Kasahara ◽  
Jun Kasuga ◽  
Shinpei Sugiura ◽  
...  

Castleman’s disease was first reported in 1954 by Castleman et al. and identified as an uncommon lymphoproliferative disorder. In most cases, Castleman’s diseases are detected in the chest, head, and neck. A 71-year-old man was referred to our hospital due to a retroperitoneal tumor in the para-aortic area by computed tomography (CT). Positron emission tomography-CT revealed an uptake in this tumor, suggesting malignant diseases. Laparoscopic tumorectomy was performed, and the pathological diagnosis was Castleman’s disease, hyaline vascular type. No evidence of recurrence was observed 20 months after surgery. We herein report a rare case of retroperitoneal Castleman’s disease.


2014 ◽  
Vol 2014 ◽  
pp. 1-5
Author(s):  
Eleftherios Spartalis ◽  
Petros Charalampoudis ◽  
Apostolos Kandilis ◽  
Antonios Athanasiou ◽  
Petros Tsaparas ◽  
...  

Castleman’s disease is a benign lymphoproliferative condition with three distinct histological subtypes. Clinically it presents in either a unicentric or multicentric manner and can affect various anatomic regions, the mediastinum being the most frequent location. We herein present a rare case of unifocal retroperitoneal mass proved to be hyaline vascular Castleman’s disease. We perform a review of the current literature pertaining to such lesions, focusing on the management of the various clinical and histological variants of the disease. Surgical excision is the treatment of choice for unifocal Castleman’s disease.


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