Cytologic and Immunophenotypic Features of Malignant Cells in Pediatric Body Fluids

2015 ◽  
Vol 59 (4) ◽  
pp. 332-338 ◽  
Author(s):  
Atif A. Ahmed ◽  
Nevene Andraws ◽  
Ahmed M. Almutairi ◽  
Hesham M. Saied ◽  
Asim M. Elbagir-Mohamed

Objective: Cytospin preparations and immunocytochemistry are common methods in hospitals to evaluate malignancies in body fluids. Characteristics of malignant cells in pediatric body fluids have not been adequately evaluated. Study Design: 183 pleural, peritoneal and pericardial pediatric fluid specimens were examined by cytospin preparations and immunocytochemistry from two hospitals using similar procedural techniques. Cytologic diagnoses were correlated with the results of clinical history, histology and ancillary studies. Results: Forty cases with malignancy were identified (21.9%); the most common diagnoses were rhabdomyosarcoma and acute lymphoblastic lymphoma (9 and 8 cases, respectively). Small round cell tumors revealed similar morphology as clusters of small round cells with central nuclei and scant cytoplasm with frequent small vacuoles. Twenty-one cases were evaluated by immunocytochemistry, 12 by flow cytometry and 5 by cytogenetic analysis. CD3, CD20, TdT, CD10, desmin and myogenin were the most common markers. Staining artifacts causing interpretation difficulties were noted in 5 cases that were resolved by molecular studies and deferral for surgical specimens. Conclusions: Small round cell tumors are the most common malignancies encountered in pediatric body fluids and share a nonspecific morphology. Although immunocytochemistry is helpful to arrive at the correct diagnosis, other ancillary studies may be necessary, particularly in hematologic malignancies and other difficult cases.

2021 ◽  
pp. 1-11
Author(s):  
Lucy M. Han ◽  
Christopher J. VandenBussche ◽  
Mads Abildtrup ◽  
Ashish Chandra ◽  
Poonam Vohra

<b><i>Background:</i></b> Small round cell tumors (SRCTs) are a broad category of diverse malignant tumors composed of monotonous undifferentiated cells. Involvement of serous fluids by SRCT is rare; however, the identification of exfoliated malignant cells is a crucial component of management and has significant implications for treatment and prognosis. The most common effusion tumors with SRCT morphology include Ewing sarcoma, synovial sarcoma, rhabdomyosarcoma (RMS), small-cell neuroendocrine carcinoma (SCNC), and desmoplastic SRCT, and the cytomorphologic distinction between these tumors is challenging. The purpose of this article is to describe the morphologic features of the most common SRCT in fluids and propose helpful ancillary testing. <b><i>Summary:</i></b> Effusion SRCTs display similar primitive and undifferentiated morphologic features although each has subtle variations. Ewing sarcoma is a mesenchymal neoplasm and harbors characteristic translocations t(11;22) (<i>EWSR1-FLI1</i>) or t(21;22) (<i>EWSR1-ERG</i>). In fluids, Ewing sarcoma shows poorly differentiated cells of variable size with round to oval nuclei, prominent nucleoli, and scant cytoplasm. In contrast, synovial sarcoma typically involves extremities and expresses a fusion transcript in t(X;18) (<i>SS18-SSX</i>). This soft tissue neoplasm demonstrates uniform cells with irregular nuclear contours, characteristic nuclear folding, and scant cytoplasm. RMS is a neoplasm arising from skeletal muscle, and the alveolar subtype demonstrates a translocation in t(2;13) (<i>PAX3-FOXO1</i>). The malignant cells show a spectrum of small round cells and pleomorphic large cells with rhabdoid morphology. RMS cells characteristically express myogenin and MyoD1, markers of skeletal muscle differentiation. Although SCNC is not a classic SRCT, the morphology is similar. SCNC demonstrates tight clusters of malignant cells with nuclear molding and salt-and-pepper chromatin. This tumor classically has neuroendocrine differentiation and is positive for synaptophysin and chromogranin on immunohistochemistry. And last, desmoplastic SRCT typically presents as an intra-abdominal mass in young men and characteristically harbors the translocation t(11;22) (p13;q12) (<i>EWSR1-WT1</i>). Cytomorphologically, the tumor shows small monomorphic cells occasionally arranged as rosette-like structures. <b><i>Key Message:</i></b> The diagnosis of SRCT can be made in effusion samples and is best achieved with a combination of morphologic features, clinical history, and ancillary testing.


2019 ◽  
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Author(s):  
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2005 ◽  
Vol 124 (suppl_1) ◽  
pp. S110-S121 ◽  
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Stacey E. Mills

2021 ◽  
Author(s):  
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S Serfling ◽  
P Mihatsch ◽  
H Hänscheid ◽  
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Rare Sarcomas ◽  
2020 ◽  
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Author(s):  
C. Honoré ◽  
O. Mir ◽  
J. Adam

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1994 ◽  
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R. Bouvier ◽  
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...  

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