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Follicular dendritic cell tumour/sarcoma: a commonly misdiagnosed tumour in the thorax.

Authors :
Viola P
Vroobel KM
Devaraj A
Jordan S
Ladas G
Dusmet M
Montero A
Rice A
Wotherspoon AC
Nicholson AG
Source :
Histopathology [Histopathology] 2016 Nov; Vol. 69 (5), pp. 752-761. Date of Electronic Publication: 2016 Jul 08.
Publication Year :
2016

Abstract

Aims: Follicular dendritic cell sarcoma is a rare tumour reported to occur occasionally in association with the hyaline-vascular type of Castleman's disease (HVCD). Most cases arise in lymph nodes, although extranodal presentation is described.<br />Methods and Results: Clinical, radiological and histological characteristics, including diagnosis on pre-resection material, were assessed in seven intrathoracic cases from five males and two females with a median age of 38 years. Clinical symptoms were related to mass location, six cases presenting within central and/or posterior mediastinal compartments and one within the lungs. Positron emission tomography-computed tomography demonstrated marked fluoro-deoxy-glucose avidity and the prominent vessels traversing the lesions. Four of six cases (67%) were misdiagnosed initially. HVCD was present in three cases. Two cases with high mitotic rates recurred after resection. All were positive for at least one of the follicular dendritic cell markers (CD21, CD35 and CD23). Six of seven cases (86%) show cyclin D1 expression ranging from 5% to 90%.<br />Conclusions: Follicular dendritic cell sarcoma is often misdiagnosed on biopsy and pathologists need to be aware of the tumour to request the relevant immunohistochemistry, especially in masses presenting in the central/posterior mediastinum with high vascularity and standardized uptake values. Background HVCD appears more common than previously thought.<br /> (© 2016 John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
1365-2559
Volume :
69
Issue :
5
Database :
MEDLINE
Journal :
Histopathology
Publication Type :
Academic Journal
Accession number :
27206572
Full Text :
https://doi.org/10.1111/his.12998