scholarly journals Lymph node fine needle Cytology in the staging and follow-up of Cutaneous Lymphomas

BMC Cancer ◽  
2014 ◽  
Vol 14 (1) ◽  
Author(s):  
Elena Vigliar ◽  
Immacolata Cozzolino ◽  
Marco Picardi ◽  
Anna Lucia Peluso ◽  
Laura Virginia Sosa Fernandez ◽  
...  
Diagnostics ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 1314
Author(s):  
Elena Vigliar ◽  
Gennaro Acanfora ◽  
Antonino Iaccarino ◽  
Massimo Mascolo ◽  
Daniela Russo ◽  
...  

Fine-needle cytology (FNC) is a useful diagnostic tool in the first line evaluation of lymphadenopathy of unknown aetiology. Nevertheless, considering the large number of conditions presenting as lymphadenopathy, lymph node cytology represents a challenging scenario. Recently, an expert panel published the proposal of the Sydney system for performing classification and reporting of lymph node cytopathology; the aim of the present study was to evaluate the applicability of this system. Thus, 300 lymph node FNCs performed over 1 year were reviewed and categorized according to the Sydney system classification. Overall, n = 20 cases (6.7%) were categorized as L1-inadequate/non-diagnostic; n = 104 (34.7%) as benign (L2); n = 25 (8.3%) as atypical (L3); n = 13 (4.3%) as suspicious (L4), and n = 138 (46%) as malignant (L5). FNC diagnoses were correlated with histopathologic and clinical follow-up to assess the diagnostic accuracy and the risk of malignancy (ROM) for each diagnostic category. Statistical analysis showed the following results: sensitivity 98.47%, specificity 95.33%, positive predictive value 96.27%, negative predictive value 98.08%, and accuracy 97.06%. The ROM was 50% for the category L1, 1.92% for L2, 58.3% for L3, and 100% for L4 and L5. In conclusion, FNC coupled with ancillary techniques ensures satisfactory diagnostic accuracy and the implementation of the Sydney system may improve the practice of cytopathologists.


Cytopathology ◽  
2019 ◽  
Vol 30 (4) ◽  
pp. 348-362 ◽  
Author(s):  
Immacolata Cozzolino ◽  
Valentina Giudice ◽  
Chiara Mignogna ◽  
Carmine Selleri ◽  
Alessandro Caputo ◽  
...  

Author(s):  
Giulio Vitagliano ◽  
Giuseppe Santoro ◽  
Luigi Landolfi ◽  
Immacolata Cozzolino ◽  
Anna L. Peluso ◽  
...  

2016 ◽  
Vol 60 (4) ◽  
pp. 372-384 ◽  
Author(s):  
Anna Lucia Peluso ◽  
Antonio Ieni ◽  
Chiara Mignogna ◽  
Pio Zeppa

Lymph node (LN) fine-needle cytology (FNC) coupled with flow cytometry immunophenotyping provides relevant information for the diagnosis of non-Hodgkin lymphoma (NHL). Numerous studies have shown FNC samples to be suitable for different molecular procedures; in this review, some of the molecular procedures most commonly employed for NHL are briefly described and evaluated in this perspective. Fluorescence in situ hybridization and chromogenic in situ hybridization are briefly described. Polymerase chain reaction (PCR)-based assays are used to identify and quantify mutations and translocations, namely immunoglobulin (IGH) and T-cell receptor rearrangements by clonality testing and IGVH somatic hypermutations either by Sanger sequencing, single-strand conformational polymorphisms or RT-PCR strategies. High-throughput technologies (HTT) encompass numerous and different diagnostic tools that share the capacity of multiple molecular investigation and sample processing in a fast and reproducible manner. HTT includes gene expression profiling, comparative genomic hybridization, single-nucleotide polymorphism arrays and next-generation sequencing technologies. A brief description of these tools and their potential application to LN FNC is reported. The challenge for FNC will be to achieve new knowledge and apply new technologies to FNC, exploiting its own basic qualities.


2016 ◽  
Vol 29 (S1) ◽  
pp. 167-171
Author(s):  
Anna Maria Cascone ◽  
Maria Siano ◽  
Basilio Angrisani ◽  
Rosa Maria Di Crescenzo ◽  
Alessandro Vatrella ◽  
...  

2007 ◽  
Vol 156 (3) ◽  
pp. 303-308 ◽  
Author(s):  
Frédéric Illouz ◽  
Patrice Rodien ◽  
Jean Paul Saint-André ◽  
Stéphane Triau ◽  
Sandrine Laboureau-Soares ◽  
...  

Objective: The usefulness of repeated fine-needle cytology (FNC) in thyroid nodules with benign cytology remains unknown. We analyzed the relevance of repeated FNC to detect suspicious or malignant (S/M) cytologies and carcinomas. Design: A retrospective study (1983–2004) was conducted in our endocrinology department. Methods: We reviewed the reports of 895 adequate FNC performed in 298 patients (298 nodules) during a mean follow-up of 5 years. We compared the nodules with at least one suspicious or malignant FNC (S/M nodules) with nodules with repeatedly benign (RB) FNC (RB nodules). Results: Among the nodules with initial benign cytology, we found 35 nodules with one or more later suspicious or malignant results. The interval between the first FNC and the first S/M FNC was 2.9 years. The probability for a nodule to have a repeated benign FNC decreases with time and with the number of FNC. We did not find any clinical or ultrasonographic characteristics related to an S/M cytology. Seven cancers were detected by the second or the third FNC with S/M results. The proportion of cancers among S/M nodules was similar when S/M cytology appears during the first, the second, or the third FNC. Conclusions: We suggest to repeat FNC up to three adequate samples in the follow-up of thyroid nodules so as not to miss the presence of malignant neoplasm.


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