期刊论文详细信息
BMC Cancer
Lymph node fine needle Cytology in the staging and follow-up of Cutaneous Lymphomas
Pio Zeppa1  Carmine Selleri1  Fabrizio Pane3  Gerardo Botti4  Antonio Vetrani2  Laura Virginia Sosa Fernandez1  Anna Lucia Peluso3  Marco Picardi3  Immacolata Cozzolino2  Elena Vigliar2 
[1]Department of Medicine and Surgery, Azienda Ospedaliera Universitaria “San Giovanni di Dio e Ruggi d’Aragona”, Largo città d’Ippocrate n.1, 84131 Salerno, (IT), Italy
[2]Departments of Advanced Biomedical Sciences of Public Health, University of Naples "Federico II", Naples, Italy
[3]Advanced Biotechnologies, Biochemistry and Medical Biotechnologies, University of Naples “Federico II”, University of Naples, CEINGE, Naples, Italy
[4]Istituto Nazionale Tumori Fondazione "G. Pascale", Naples, Italy
关键词: PCR;    Flow cytometry;    Fine needle cytology;    Cutaneous lymphoma;    Lymph node;   
Others  :  859165
DOI  :  10.1186/1471-2407-14-8
 received in 2013-03-22, accepted in 2013-12-13,  发布年份 2014
PDF
【 摘 要 】

Background

Lymph nodal involvement is an important clinical-pathological sign in primary cutaneous lymphoma (PCL), as it marks the transformation/evolution of the disease from localized to systemic; therefore the surveillance of lymph nodes is important in the staging and follow up of PCL. Fine needle cytology (FNC) is widely used in the diagnosis of lymphadenopathies but has rarely been reported in PCL staging and follow-up. In this study an experience on reactive and neoplastic lymphadenopathies arisen in PCL and investigated by FNC, combined to ancillary techniques, is reported.

Methods

Twenty-one lymph node FNC from as many PCL patients were retrieved; 17 patients had mycosis fungoides (MF) and 4 a primary cutaneous B-cell lymphoma (PBL). In all cases, rapid on site evaluation (ROSE) was performed and additional passes were used to perform flow cytometry (FC), immunocytochemistry (ICC) and/or polymerase chain reaction (PCR) to assess or rule out a possible clonality of the corresponding cell populations.

Results

FNC combined with FC, ICC, and PCR identified 12 cases of reactive, non specific, hyperplasia (BRH), 4 dermatopathic lymphadenopathy (DL), 4 lymph nodal involvement by MF and 1 lymph nodal involvement by cutaneous B-cell lymphoma.

Conclusions

FNC coupled with ancillary techniques is an effective tool to evaluate lymph node status in PCL patients, provided that ROSE and a rational usage of ancillary techniques is performed according to the clinical context and the available material. The method can be reasonably used as first line procedure in PCL staging and follow up, avoiding expensive and often ill tolerated biopsies when not strictly needed.

【 授权许可】

   
2014 Vigliar et al.; licensee BioMed Central Ltd.

【 预 览 】
附件列表
Files Size Format View
20140724081735167.pdf 2217KB PDF download
163KB Image download
163KB Image download
171KB Image download
【 图 表 】

【 参考文献 】
  • [1]Kempf W, Sander CA: Classification of cutaneous lymphomas - an update. Histopathology 2010, 56:57-70.
  • [2]Willemze R, Jaffe ES, Burg G, et al.: WHO-EORTC classification for cutaneous lymphomas. Blood 2005, 105:3768-3785.
  • [3]UICC, et al.: TNM Classification of Malignant Tumors. 7th edition. New York: Wiley-Liss; 2010.
  • [4]AJCC: AJCC Cancer Staging Manual. 7th edition. New York: Springer; 2010.
  • [5]Olsen E, Vonderheid E, Pimpinelli N, et al.: Revisions to the staging and classification of mycosis fungoides and Sezary syndrome: a proposal of the International Society for Cutaneous Lymphomas (ISCL) and the cutaneous lymphoma task force of the European Organization of Research and Treatment of Cancer (EORTC). Blood 2007, 110:1713-1722.
  • [6]Kim YH, Willemze R, Pimpinelli N, et al.: TNM classification system for primary cutaneous lymphomas other than mycosis fungoides and Sezary syndrome: a proposal of the International Society for Cutaneous Lymphomas (ISCL) and the Cutaneous Lymphoma Task Force of the European Organization of Research and Treatment of Cancer (EORTC). Blood 2007, 110:479-484.
  • [7]Kim YH, Liu HL, Mraz-Gernhard S, et al.: Long-term outcome of 525 patients with mycosis fungoides and Sezary syndrome: clinical prognostic factors and risk for disease progression. Arch Dermatol 2003, 139:857-866.
  • [8]Zeppa P, Vigliar E, Cozzolino I, et al.: Fine needle aspiration cytology and flow cytometry immunophenotyping of non-Hodgkin lymphoma: can we do better? Cytopathology 2010, 21:300-310.
  • [9]Zeppa P, Marino G, Troncone G, et al.: Fine-needle cytology and flow cytometry immunophenotyping and subclassification of non-Hodgkin lymphoma: a critical review of 307 cases with technical suggestions. Cancer 2004, 102:55-65.
  • [10]Galindo LM, Garcia FU, Hanau CA, et al.: Fine-needle aspiration biopsy in the evaluation of lymphadenopathy associated with cutaneous T-cell lymphoma (mycosis fungoides/Sézary syndrome). Am J Clin Pathol 2000, 113:865-871.
  • [11]Pai RK, Mullins FM, Kim YH, Kong CS: Cytologic evaluation of lymphadenopathy associated with mycosis fungoides and Sezary syndrome: role of immunophenotypic and molecular ancillary studies. Cancer 2008, 114:323-332.
  • [12]Vonderheid EC, Bernengo MG, Burg G, et al.: Update on erythrodermic cutaneous T-cell lymphoma: report of the International Society for Cutaneous Lymphomas. J Am Acad Dermatol 2002, 46:95-106.
  • [13]Fraser-Andrews EA, Mitchell T, Ferreira S, Seed PT, Russell-Jones R, Calonje E, Whittaker SJ: Molecular staging of lymph nodes from 60 patients with mycosis fungoides and Sézary syndrome: correlation with histopathology and outcome suggests prognostic relevance in mycosis fungoides. Br J Dermatol 2006, 155:756-762.
  • [14]Leenders MW, Broeders M, Croese C, Richir MC, Go HL, Langenhorst BL, Meijer S, Schreurs WH: Ultrasound and fine needle aspiration cytology of axillary lymph nodes in breast cancer. To do or not to do? Breast 2012, 21:578-583.
  • [15]Lam TK, Uren RF, Scolyer RA, Quinn MJ, Shannon KF, Thompson JF: False-negative sentinel node biopsy because of obstruction of lymphatics by metastatic melanoma: the value of ultrasound in conjunction with preoperative lymphoscintigraphy. Melanoma Res 2009, 19:94-99.
  • [16]Jegalian AG, Eberle FC, Pack SD, Mirvis M, Raffeld M, Pittaluga S, Jaffe ES: Follicular lymphoma in situ: clinical implications and comparisons with partial involvement by follicular lymphoma. Blood 2011, 118:2976-2984.
  • [17]da Cunha SG, Ko HM, Saieg MA, Geddie WR: "The petals and thorns" of ROSE (rapid on-site evaluation). Cancer Cytopathol 2012, 121:4-8.
  • [18]Young NA, Al-Saleem TI, Ehya H, Smith MR: Utilization of fine-needle aspiration cytology and flow cytometry in the diagnosis and sub-classification of primary and recurrent lymphoma. Cancer 1998, 84:252-261.
  • [19]Kaleem Z, White G, Vollmer RT: Critical analysis and diagnostic usefulness of limited immunophenotyping of B-cell non-Hodgkin lymphomas by flow cytometry. Am JClin Pathol. 2001, 115:136-142.
  • [20]Dey P: Role of ancillary techniques in diagnosing and subclassifying non-Hodgkin's lymphomas on fine needle aspiration cytology. Cytopathology 2006, 17:275-287.
  • [21]Arber DA, Braziel RM, Bagg A, Bijwaard KE: Evaluation of T cell receptor testing in lymphoid neoplasms: results of a multicenter study of 29 extracted DNA and paraffin-embedded samples. J Mol Diagn 2001, 3:133-140.
  • [22]Delfau-Larue MH, Laroche L, Wechsler J, et al.: Diagnostic value of dominant T-cell clones in peripheral blood in 363 patients presenting consecutively with a clinical suspicion of cutaneous lymphoma. Blood 2000, 96:2987-2992.
  • [23]Langerak AW, Groenen PJ, Brüggemann M, et al.: EuroClonality/BIOMED-2 guidelines for interpretation and reporting of Ig/TCR clonality testing in suspected lymphoproliferations. Leukemia 2012, 26:2159-2171. Review
  • [24]Van Dongen JJ, Langerak AW: Bru¨ggemann M et al. Design and standardization of PCR primers and protocols for detection of clonal immunoglobulin and T-cell receptor gene recombinations in suspect lymphoproliferations: report of the BIOMED-2 Concerted Action BMH4-CT98-3936. Leukemia 2003, 17:2257-2317.
  文献评价指标  
  下载次数:41次 浏览次数:36次