Journal of Cytology
Home About us Ahead of print Instructions Submission Subscribe Advertise Contact e-Alerts Login 
Users Online:232
  Print this page  Email this page Small font sizeDefault font sizeIncrease font size


 
 Table of Contents    
LETTER TO EDITOR  
Year : 2021  |  Volume : 38  |  Issue : 2  |  Page : 110-111
Inguinal lymph node metastasis in a case of recurrent biphasic synovial sarcoma-A cytologic diagnosis


1 Department of Pathology, Kalinga Institute of Medical Sciences, Bhubaneswar, Odisha, India
2 Department of Oncosurgery, Kalinga Institute of Medical Sciences, Bhubaneswar, Odisha, India

Click here for correspondence address and email

Date of Submission03-Jun-2020
Date of Decision21-Jun-2020
Date of Acceptance23-Mar-2021
Date of Web Publication10-May-2021
 

How to cite this article:
Bose A, Pradhan P, Dash K, Senapati U, Sahoo SR, Parida S. Inguinal lymph node metastasis in a case of recurrent biphasic synovial sarcoma-A cytologic diagnosis. J Cytol 2021;38:110-1

How to cite this URL:
Bose A, Pradhan P, Dash K, Senapati U, Sahoo SR, Parida S. Inguinal lymph node metastasis in a case of recurrent biphasic synovial sarcoma-A cytologic diagnosis. J Cytol [serial online] 2021 [cited 2021 Jun 18];38:110-1. Available from: https://www.jcytol.org/text.asp?2021/38/2/110/315769




Synovial sarcomas (SS) are soft tissue tumors (STT) of unknown mesenchymal origin.[1] Not all sarcomas metastasize to lymph nodes with regional lymph node metastasis being less frequently encountered.[2] Here, we present cytologic diagnosis of a case of recurrent SS with an inguinal lymph node metastasis.

A 33-year-old male presented with pain in the left foot for the last 3 months. Examination revealed a scar over the left foot and minimal inguinal lymphadenopathy. Ultrasonography (USG) of the left inguinal region showed enlarged lymph nodes; one with necrotic center suspicious of metastatic deposit. USG-guided FNAC from the same showed moderately cellular smears comprising of loosely cohesive clusters of oval to spindle cells, nuclear atypia, bland chromatin, inconspicuous nucleoli and minimal pleomorphism [Figure 1]a and [Figure 1]b. A distinct second population of round cells arranged in acinar pattern were recognized, having central to eccentric, round nuclei, fine nuclear chromatin and scant to moderate cytoplasm [[Figure 1]b, inset]. Few bare nuclei, mast cells and reactive lymphoid cells were also seen along with necrosis, suspicious of a metastatic spindle-cell sarcoma. A detailed history revealed a similar history 3 years back for which he was operated twice. Previous biopsy and immunohistochemistry slides were reviewed which revealed a high-grade biphasic-SS, positive for vimentin, CK7, epithelial membrane antigen(EMA), CD99, Bcl-2 and negative for S-100 and smooth muscle actin (SMA) [Figure 1]c, [Figure 1]d, [Figure 1]e, [Figure 1]f, [Figure 1]g, [Figure 1]h. As the FNAC material was insufficient, ancillary techniques could not be performed. He defaulted chemotherapy and had presented after an interval of 11 months, so possibility of a metastatic biphasic-SS was suggested. Patient was referred for adjuvant therapy.
Figure 1: Cytosmears showing high cellularity with loosely cohesive clusters of spindle cells with thin vascular fragments (a), dyscohesive cell, singly lying ovoid to spindle cells showing minimal pleomorphism (b). Inset (b) shows round tumor cells showing glandular pattern of arrangement. Histopathology showed spindle cells (c) with expression of vimentin (d), CD99 (e), EMA (f), Bcl-2 (h) and negative for S-100 (g). [a-h: 400X]

Click here to view


SS is a STT, manifesting epithelioid differentiation. Earlier understanding suggested that the tumor took origin from synovium, while the current understanding recategorizes the same as an STT of uncertain differentiation.[1] It is a high grade, relatively chemoresponsive tumor with a specific translocation t(x; 18) (p11.2; q11.2).[3] Sarcomas metastasize conventionally through the hematogenous route. Those which spread to lymph nodes include rhabdomyo-, angio-, clear cell, epithelioid- and synovial-sarcoma. This case is unusual in exhibiting nodal metastasis as SSs show it in 1-50% cases.[2],[4],[5] Current guidelines recommend SSs to be classified in an intermediate-group called the 'potential-risk' histology. Lymph node involvement is poor prognostic factor, sign of dissemination and aggressiveness.[5]

SSs are hypercellular with cohesive clusters, monotonous oval bland nuclei, granular chromatin and prominent nucleoli. Mitoses, necrosis or even rhabdoid cells may be noted.[1],[3] In this particular case, it has been highlighted that in biphasic-SS, tumor cells may be in glandular pattern with mast cells in a reactive lymphoid background. Presence of epithelial component helps but is infrequent. Presence of myxoid stroma and heterogeneous lesions helps in distinguishing SS from myoepithelial carcinomas.[6] 'Cigar-shaped' and 'buckled' nuclei help in differentiating from leiomyosarcoma and malignant peripheral nerve sheath tumor, respectively.[6] SSs express vimentin, cytokeratin, EMA and Bcl-2 while they are negative for SMA and S-100.[6] As is shown by this case, USG can be beneficial in evaluation, aspiration and biopsies of suspicious lymph nodes.[5] In addition, this case emphasizes a detailed clinical history and careful cytomorphologic assessment to identify the biphasic components along with soft pointers, use of immunomarkers and biopsy correlation for making an accurate diagnosis.

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.



 
   References Top

1.
Pyden AD, Lin X. Synovial sarcoma presenting as a lung mass and diagnosed by cytology. Diagn Cytopathol 2016;44:434-7.  Back to cited text no. 1
    
2.
Nelen SD, Vogelaar FJ, Gilissen F, Van der Linden JC, Bosscha K. Lymph node metastasis after a soft tissue sarcoma of the leg: A case report and a review of the literature. Case Rep Surg 2013;2013:930361.  Back to cited text no. 2
    
3.
Rekhi B, Shetty O, Ramadwar M, Rangarajan V, Bajpai J. Role of fine needle aspiration cytology in the diagnosis of a rare case of a poorly differentiated synovial sarcoma with “Rhabdoid” features, including treatment implications. Diagn Cytopathol 2017;45:662-7.  Back to cited text no. 3
    
4.
Crettenand F, Martin D, Cherix S, Demartines N, Matter M. Occurrence and prognosis of lymph node metastases in patients selected for isolated limb perfusion with soft tissue sarcoma. J Cancer. 2018;9:3311-5.  Back to cited text no. 4
    
5.
Rosenthal J, Cardona K, Sayyid SK, Perricone AJ, Reimer N, Monson D, et al. Nodal metastases of soft tissue sarcomas: Risk factors, imaging findings, and implications. Skeletal Radiol 2020;49:221-9.  Back to cited text no. 5
    
6.
Díaz Del Arco C, Fernández Aceñero MJ. Biphasic axillary synovial sarcoma diagnosed by preoperative fine-needle aspiration cytology. Diagn Cytopathol 2017;45:857-60.  Back to cited text no. 6
    

Top
Correspondence Address:
Dr. Prita Pradhan
Department of Pathology, Kalinga Institute of Medical Sciences, Bhubaneswar - 751 024, Odisha
India
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/JOC.JOC_51_20

Rights and Permissions


    Figures

  [Figure 1]



 

Top
 
 
  Search
 
  
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
    Email Alert *
    Add to My List *
* Registration required (free)  


    References
    Article Figures

 Article Access Statistics
    Viewed168    
    Printed3    
    Emailed0    
    PDF Downloaded15    
    Comments [Add]    

Recommend this journal