scholarly journals Angioimmunoblastic T-Cell Lymphoma: A Questionable Association with Follicular Dendritic Cell Sarcoma

2017 ◽  
Vol 2017 ◽  
pp. 1-4
Author(s):  
Daniel Benharroch ◽  
Miriam Zekzer ◽  
Karen Nalbandyan

An elderly woman presented with generalized lymphadenopathy, several systemic symptoms, and splenomegaly. An inguinal lymph node excision revealed a compound picture. One aspect of the lymph node morphology, including cells with follicular T-helper cell phenotype, was most consistent with angioimmunoblastic T-cell lymphoma. The other component, revealing spindle cells forming whorls with immunostaining for CD21, CD23, and fascin, might be an integral part of this T-cell lymphoma. However, due to the often massive involvement of the nodal tissue by these follicular dendritic cells, these areas were questionably suggestive of involvement by follicular dendritic cell sarcoma. We raise herein the issue of the borderline area between advanced follicular dendritic cell expansion in angioimmunoblastic T-cell lymphoma and a massive follicular dendritic cell proliferation consistent with follicular dendritic cells sarcoma, in the absence of a genomic analysis.

2015 ◽  
Vol 55 (2) ◽  
pp. 61-69 ◽  
Author(s):  
Haruo Ohtani ◽  
Takuya Komeno ◽  
Yoshiko Agatsuma ◽  
Motohiro Kobayashi ◽  
Masayuki Noguchi ◽  
...  

2009 ◽  
Vol 59 (11) ◽  
pp. 809-812 ◽  
Author(s):  
Yosuke Yamada ◽  
Hironori Haga ◽  
Mako Hernandez ◽  
Kanako C. Kubota ◽  
Fumika Orii ◽  
...  

2016 ◽  
Vol 140 (2) ◽  
pp. 186-190 ◽  
Author(s):  
Annie Wu ◽  
Sheeja Pullarkat

Follicular dendritic cell sarcoma is an uncommon neoplastic proliferation of spindled to ovoid cells with morphologic and immunophenotypic features similar to normal follicular dendritic cells. While most follicular dendritic cell sarcomas arise from lymph nodes, at least one-third occur in extranodal sites. A broad differential diagnosis can be developed—as this tumor has morphologic features similar to other tumors, hence creating a diagnostic pitfall—but its immunophenotypic profile is quite specific and is diagnostically crucial. Herein, we review the pathogenesis; histologic morphology; and immunohistochemical, electron microscopy, and clinical features, including treatment and prognosis, of follicular dendritic cell sarcomas. We will briefly describe the role of molecular studies including utility of BRAF mutations in diagnosing this tumor.


2008 ◽  
Vol 132 (10) ◽  
pp. 1683-1687 ◽  
Author(s):  
Kenneth E. Youens ◽  
Michael S. Waugh

Abstract Extranodal follicular dendritic cell sarcoma is a rare tumor of follicular dendritic cells that can occur in a wide variety of sites. Although fairly well characterized histologically, with a distinct immunophenotype, it remains underrecognized, with as many as one third of cases initially misdiagnosed. This is often due to a failure to consider the entity. Patients with this tumor may have a worse prognosis than originally described. Prompted by a recent case at our institution, we briefly review the clinical features, etiology, histologic, and cytologic appearance of the tumor, as well as the ancillary studies useful in resolving diagnostic issues, primarily in an attempt to increase recognition of this rare neoplasm.


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